{"database": "metadata", "table": "run_metadata", "is_view": false, "human_description_en": "where experiment.library_layout = \"PAIRED\", technology = \"10x\" and tissue_curation_coarse = \"Cancer or Tumor\"", "rows": [[61554, "SRR14804251", "SRX11137027", "SRS9200152", "SRP287858", "PRJNA670235", "Spatially resolved transcriptomics reveals the architecture of the tumor microenvironment interface", "GSE159709", "Transcriptome Analysis", "Cancer cells interact with a wide variety of other cell types  but our understanding of microenvironmental heterogeneity and how it influences tumor phenotypes is limited. While single cell RNA seq scRNA seq has helped define these TME cell types  it provides limited information on the mechanisms that define how individual tumor cells interact with TME. Here  we integrate spatial transcriptomics with scRNA seq to define the architecture and nature of nascent tumor and surrounding microenvironment cells as they come into contact through the process of invasion. Using a well defined transgenic zebrafish model of BRAFV600E driven melanoma  we identify a transcriptionally unique \u201cinterface\u201d cluster localized at the boundary between tumor cells and surrounding tissues. Using an unbiased  data driven approach  we identify spatially patterned gene modules specific to the interface and show that the interface is a distinct transcriptional entity that histologically resembles the microenvironment but transcriptionally resembles the tumor. By complementing ST with scRNA seq  we demonstrate that the interface is composed of specialized tumor and microenvironment cells. Both cell types in the interface upregulate a common set of cilia genes  and we find enrichment of cilia proteins only where the tumor meets the TME. Cilia gene expression is regulated by ETS family transcription factors  which normally act to suppress their expression outside of this region. This unique ETS driven interface transcriptional state is conserved across ten different human patient samples  suggesting this is a conserved feature of human melanoma. Taken together  our results demonstrate the power of spatial and single cell transcriptomics techniques in uncovering novel biological mechanisms that drive tumor invasion into new tissues.  Overall design: Spatial transcriptomics Visium platform of zebrafish bearing BRAF V600E driven melanomas. Single cell RNA seq 10X Genomics v3 of two such zebrafish. Single nucleus RNA seq 10X Genomics v3 of three such zebrafish pooled into one reaction.", null, "pubmed:34725363", null, "Nuc seq", "GSM5380072", null, "tissue:Zebrafish melanomas BRAF V600E|sample type:Single nucleus suspension", "Nuc seq", "Illumina RTA v2 software was used for basecalling and quality determination. The 10x Genomics three prime v3 raw FASTQ data was processed using 10X Genomics proprietary CellRanger v5.0.1 pipeline. Genome build: GRCz10.88 Supplementary files format and content: For 10x Genomics three prime GEX v3 data: output of CellRanger pipeline including gene expression matrix  features and barcodes.", "Zebrafish melanomas BRAF V600E", null, "Adult tumor bearing fish were dissected to obtain only the tumor and surrounding tissues i.e head and tail were removed. The tissue was then ground in a Dounce homogenizer on ice in Nuclei EZ Prep Lysis Buffer Sigma Aldrich #NUC101. The nuclear suspension was then spun down at 4\u00b0C 500g  5 min. post resuspending the pellet in 1 mL wash buffer 250 mM sucrose  50 mM citric acid  1% BSA  20 mM DTT  0.2U/\u00b5L RNAse inhibitor  the sample was again spun at 4\u00b0C for 5 min at 500g. The pellet was resuspended in 1 mL wash buffer and subsequently sorted at 4\u00b0C to isolate individual nuclei  using a BD FACSAria III cell sorter BD Biosciences. Approximately equal numbers of GFP+ tumor and GFP  microenvironment nuclei were collected. Equal numbers of sorted GFP+ tumor and GFP  microenvironment nuclei were centrifuged at 600g for 5 minutes at 4\u00b0C. Droplet based snRNA seq was performed using the Chromium Single Cell 3\u2019 Library & Gel Bead Kit v3 10X Genomics and Chromium Single Cell 3\u2019 Chip G 10X Genomics. Approximately 12 000 nuclei were encapsulated in a single v3 reaction. GEM generation and library preparation were performed according to manufacturer\u2019s instructions.\u00a0", null, "sample type:Single nucleus suspension", "GSM5380072", "GSM5380072: Nuc seq; Danio rerio; RNA Seq", "GSM5380072", null, "1", "Adult tumor bearing fish were dissected to obtain only the tumor and surrounding tissues i.e head and tail were removed. The tissue was then ground in a Dounce homogenizer on ice in Nuclei EZ Prep Lysis Buffer Sigma Aldrich #NUC101. The nuclear suspension was then spun down at 4\u00b0C 500g  5 min. post resuspending the pellet in 1 mL wash buffer 250 mM sucrose  50 mM citric acid  1% BSA  20 mM DTT  0.2U/\u00b5L RNAse inhibitor  the sample was again spun at 4\u00b0C for 5 min at 500g. The pellet was resuspended in 1 mL wash buffer and subsequently sorted at 4\u00b0C to isolate individual nuclei  using a BD FACSAria III cell sorter BD Biosciences. Approximately equal numbers of GFP+ tumor and GFP  microenvironment nuclei were collected. Equal numbers of sorted GFP+ tumor and GFP  microenvironment nuclei were centrifuged at 600g for 5 minutes at 4\u00b0C. Droplet based snRNA seq was performed using the Chromium Single Cell three prime Library & Gel Bead Kit v3 10X Genomics and Chromium Single Cell three prime Chip G 10X Genomics. Approximately 12 000 nuclei were encapsulated in a single v3 reaction. GEM generation and library preparation were performed according to manufacturer's instructions.", "GEO Accession:GSM5380072", "RNA-Seq", "TRANSCRIPTOMIC", "cDNA", "PAIRED", "ILLUMINA", "Illumina NovaSeq 6000", null, "SRP287858", null, null, "2498_Zebrafish_IGO_11175_B_17_S16_L001_R1_001.fastq-001.gz 2498_Zebrafish_IGO_11175_B_17_S16_L001_R2_001.fastq-003.gz", "fastq fastq", 16881438541.0, 139516021.0, "GSM5380072 r1", "0:29 1:92", "A:4751346944;C:3672149977;G:3866179079;T:4591370192;N:392349", 29, 92, null, null, 4751346944, 3672149977, 3866179079, 4591370192, 392349, "SRX11137027", "SRS9200152", "SRA1145723", "GEO", "Memorial Sloan Kettering Cancer Center", 2, 0.0064, 0.82934, 0.00273, 0.1289, 0.99462, 0.75615, 0.43651, 0.54303, 29, 92, "T", "B", "sc-like readlen", "illumina", "novaseq_era", "unknown", "cdna_unspecified", "unknown", "sc", "single_cell_droplet", "10x", null, "United States", "2021-06-14", "Adult", "Adult", "Cancer or Tumor", "Cancer or Tumor"], [61555, "SRR14804252", "SRX11137027", "SRS9200152", "SRP287858", "PRJNA670235", "Spatially resolved transcriptomics reveals the architecture of the tumor microenvironment interface", "GSE159709", "Transcriptome Analysis", "Cancer cells interact with a wide variety of other cell types  but our understanding of microenvironmental heterogeneity and how it influences tumor phenotypes is limited. While single cell RNA seq scRNA seq has helped define these TME cell types  it provides limited information on the mechanisms that define how individual tumor cells interact with TME. Here  we integrate spatial transcriptomics with scRNA seq to define the architecture and nature of nascent tumor and surrounding microenvironment cells as they come into contact through the process of invasion. Using a well defined transgenic zebrafish model of BRAFV600E driven melanoma  we identify a transcriptionally unique \u201cinterface\u201d cluster localized at the boundary between tumor cells and surrounding tissues. Using an unbiased  data driven approach  we identify spatially patterned gene modules specific to the interface and show that the interface is a distinct transcriptional entity that histologically resembles the microenvironment but transcriptionally resembles the tumor. By complementing ST with scRNA seq  we demonstrate that the interface is composed of specialized tumor and microenvironment cells. Both cell types in the interface upregulate a common set of cilia genes  and we find enrichment of cilia proteins only where the tumor meets the TME. Cilia gene expression is regulated by ETS family transcription factors  which normally act to suppress their expression outside of this region. This unique ETS driven interface transcriptional state is conserved across ten different human patient samples  suggesting this is a conserved feature of human melanoma. Taken together  our results demonstrate the power of spatial and single cell transcriptomics techniques in uncovering novel biological mechanisms that drive tumor invasion into new tissues.  Overall design: Spatial transcriptomics Visium platform of zebrafish bearing BRAF V600E driven melanomas. Single cell RNA seq 10X Genomics v3 of two such zebrafish. Single nucleus RNA seq 10X Genomics v3 of three such zebrafish pooled into one reaction.", null, "pubmed:34725363", null, "Nuc seq", "GSM5380072", null, "tissue:Zebrafish melanomas BRAF V600E|sample type:Single nucleus suspension", "Nuc seq", "Illumina RTA v2 software was used for basecalling and quality determination. The 10x Genomics three prime v3 raw FASTQ data was processed using 10X Genomics proprietary CellRanger v5.0.1 pipeline. Genome build: GRCz10.88 Supplementary files format and content: For 10x Genomics three prime GEX v3 data: output of CellRanger pipeline including gene expression matrix  features and barcodes.", "Zebrafish melanomas BRAF V600E", null, "Adult tumor bearing fish were dissected to obtain only the tumor and surrounding tissues i.e head and tail were removed. The tissue was then ground in a Dounce homogenizer on ice in Nuclei EZ Prep Lysis Buffer Sigma Aldrich #NUC101. The nuclear suspension was then spun down at 4\u00b0C 500g  5 min. post resuspending the pellet in 1 mL wash buffer 250 mM sucrose  50 mM citric acid  1% BSA  20 mM DTT  0.2U/\u00b5L RNAse inhibitor  the sample was again spun at 4\u00b0C for 5 min at 500g. The pellet was resuspended in 1 mL wash buffer and subsequently sorted at 4\u00b0C to isolate individual nuclei  using a BD FACSAria III cell sorter BD Biosciences. Approximately equal numbers of GFP+ tumor and GFP  microenvironment nuclei were collected. Equal numbers of sorted GFP+ tumor and GFP  microenvironment nuclei were centrifuged at 600g for 5 minutes at 4\u00b0C. Droplet based snRNA seq was performed using the Chromium Single Cell 3\u2019 Library & Gel Bead Kit v3 10X Genomics and Chromium Single Cell 3\u2019 Chip G 10X Genomics. Approximately 12 000 nuclei were encapsulated in a single v3 reaction. GEM generation and library preparation were performed according to manufacturer\u2019s instructions.\u00a0", null, "sample type:Single nucleus suspension", "GSM5380072", "GSM5380072: Nuc seq; Danio rerio; RNA Seq", "GSM5380072", null, "1", "Adult tumor bearing fish were dissected to obtain only the tumor and surrounding tissues i.e head and tail were removed. The tissue was then ground in a Dounce homogenizer on ice in Nuclei EZ Prep Lysis Buffer Sigma Aldrich #NUC101. The nuclear suspension was then spun down at 4\u00b0C 500g  5 min. post resuspending the pellet in 1 mL wash buffer 250 mM sucrose  50 mM citric acid  1% BSA  20 mM DTT  0.2U/\u00b5L RNAse inhibitor  the sample was again spun at 4\u00b0C for 5 min at 500g. The pellet was resuspended in 1 mL wash buffer and subsequently sorted at 4\u00b0C to isolate individual nuclei  using a BD FACSAria III cell sorter BD Biosciences. Approximately equal numbers of GFP+ tumor and GFP  microenvironment nuclei were collected. Equal numbers of sorted GFP+ tumor and GFP  microenvironment nuclei were centrifuged at 600g for 5 minutes at 4\u00b0C. Droplet based snRNA seq was performed using the Chromium Single Cell three prime Library & Gel Bead Kit v3 10X Genomics and Chromium Single Cell three prime Chip G 10X Genomics. Approximately 12 000 nuclei were encapsulated in a single v3 reaction. GEM generation and library preparation were performed according to manufacturer's instructions.", "GEO Accession:GSM5380072", "RNA-Seq", "TRANSCRIPTOMIC", "cDNA", "PAIRED", "ILLUMINA", "Illumina NovaSeq 6000", null, "SRP287858", null, null, "2498_Zebrafish_IGO_11175_B_17_S16_L002_R1_001.fastq-002.gz 2498_Zebrafish_IGO_11175_B_17_S16_L002_R2_001.fastq-004.gz", "fastq fastq", 16950408541.0, 140086021.0, "GSM5380072 r2", "0:29 1:92", "A:4767053400;C:3688816562;G:3885746735;T:4608355293;N:436551", 29, 92, null, null, 4767053400, 3688816562, 3885746735, 4608355293, 436551, "SRX11137027", "SRS9200152", "SRA1145723", "GEO", "Memorial Sloan Kettering Cancer Center", 2, 0.00657, 0.8291, 0.00269, 0.12832, 0.9946, 0.75657, 0.45883, 0.54175, 29, 92, "T", "B", "sc-like readlen", "illumina", "novaseq_era", "unknown", "cdna_unspecified", "unknown", "sc", "single_cell_droplet", "10x", null, "United States", "2021-06-14", "Adult", "Adult", "Cancer or Tumor", "Cancer or Tumor"], [61556, "SRR14804253", "SRX11137027", "SRS9200152", "SRP287858", "PRJNA670235", "Spatially resolved transcriptomics reveals the architecture of the tumor microenvironment interface", "GSE159709", "Transcriptome Analysis", "Cancer cells interact with a wide variety of other cell types  but our understanding of microenvironmental heterogeneity and how it influences tumor phenotypes is limited. While single cell RNA seq scRNA seq has helped define these TME cell types  it provides limited information on the mechanisms that define how individual tumor cells interact with TME. Here  we integrate spatial transcriptomics with scRNA seq to define the architecture and nature of nascent tumor and surrounding microenvironment cells as they come into contact through the process of invasion. Using a well defined transgenic zebrafish model of BRAFV600E driven melanoma  we identify a transcriptionally unique \u201cinterface\u201d cluster localized at the boundary between tumor cells and surrounding tissues. Using an unbiased  data driven approach  we identify spatially patterned gene modules specific to the interface and show that the interface is a distinct transcriptional entity that histologically resembles the microenvironment but transcriptionally resembles the tumor. By complementing ST with scRNA seq  we demonstrate that the interface is composed of specialized tumor and microenvironment cells. Both cell types in the interface upregulate a common set of cilia genes  and we find enrichment of cilia proteins only where the tumor meets the TME. Cilia gene expression is regulated by ETS family transcription factors  which normally act to suppress their expression outside of this region. This unique ETS driven interface transcriptional state is conserved across ten different human patient samples  suggesting this is a conserved feature of human melanoma. Taken together  our results demonstrate the power of spatial and single cell transcriptomics techniques in uncovering novel biological mechanisms that drive tumor invasion into new tissues.  Overall design: Spatial transcriptomics Visium platform of zebrafish bearing BRAF V600E driven melanomas. Single cell RNA seq 10X Genomics v3 of two such zebrafish. Single nucleus RNA seq 10X Genomics v3 of three such zebrafish pooled into one reaction.", null, "pubmed:34725363", null, "Nuc seq", "GSM5380072", null, "tissue:Zebrafish melanomas BRAF V600E|sample type:Single nucleus suspension", "Nuc seq", "Illumina RTA v2 software was used for basecalling and quality determination. The 10x Genomics three prime v3 raw FASTQ data was processed using 10X Genomics proprietary CellRanger v5.0.1 pipeline. Genome build: GRCz10.88 Supplementary files format and content: For 10x Genomics three prime GEX v3 data: output of CellRanger pipeline including gene expression matrix  features and barcodes.", "Zebrafish melanomas BRAF V600E", null, "Adult tumor bearing fish were dissected to obtain only the tumor and surrounding tissues i.e head and tail were removed. The tissue was then ground in a Dounce homogenizer on ice in Nuclei EZ Prep Lysis Buffer Sigma Aldrich #NUC101. The nuclear suspension was then spun down at 4\u00b0C 500g  5 min. post resuspending the pellet in 1 mL wash buffer 250 mM sucrose  50 mM citric acid  1% BSA  20 mM DTT  0.2U/\u00b5L RNAse inhibitor  the sample was again spun at 4\u00b0C for 5 min at 500g. The pellet was resuspended in 1 mL wash buffer and subsequently sorted at 4\u00b0C to isolate individual nuclei  using a BD FACSAria III cell sorter BD Biosciences. Approximately equal numbers of GFP+ tumor and GFP  microenvironment nuclei were collected. Equal numbers of sorted GFP+ tumor and GFP  microenvironment nuclei were centrifuged at 600g for 5 minutes at 4\u00b0C. Droplet based snRNA seq was performed using the Chromium Single Cell 3\u2019 Library & Gel Bead Kit v3 10X Genomics and Chromium Single Cell 3\u2019 Chip G 10X Genomics. Approximately 12 000 nuclei were encapsulated in a single v3 reaction. GEM generation and library preparation were performed according to manufacturer\u2019s instructions.\u00a0", null, "sample type:Single nucleus suspension", "GSM5380072", "GSM5380072: Nuc seq; Danio rerio; RNA Seq", "GSM5380072", null, "1", "Adult tumor bearing fish were dissected to obtain only the tumor and surrounding tissues i.e head and tail were removed. The tissue was then ground in a Dounce homogenizer on ice in Nuclei EZ Prep Lysis Buffer Sigma Aldrich #NUC101. The nuclear suspension was then spun down at 4\u00b0C 500g  5 min. post resuspending the pellet in 1 mL wash buffer 250 mM sucrose  50 mM citric acid  1% BSA  20 mM DTT  0.2U/\u00b5L RNAse inhibitor  the sample was again spun at 4\u00b0C for 5 min at 500g. The pellet was resuspended in 1 mL wash buffer and subsequently sorted at 4\u00b0C to isolate individual nuclei  using a BD FACSAria III cell sorter BD Biosciences. Approximately equal numbers of GFP+ tumor and GFP  microenvironment nuclei were collected. Equal numbers of sorted GFP+ tumor and GFP  microenvironment nuclei were centrifuged at 600g for 5 minutes at 4\u00b0C. Droplet based snRNA seq was performed using the Chromium Single Cell three prime Library & Gel Bead Kit v3 10X Genomics and Chromium Single Cell three prime Chip G 10X Genomics. Approximately 12 000 nuclei were encapsulated in a single v3 reaction. GEM generation and library preparation were performed according to manufacturer's instructions.", "GEO Accession:GSM5380072", "RNA-Seq", "TRANSCRIPTOMIC", "cDNA", "PAIRED", "ILLUMINA", "Illumina NovaSeq 6000", null, "SRP287858", null, null, "2498_Zebrafish_HTO_IGO_11175_B_18_S18_L001_R1_001.fastq.gz 2498_Zebrafish_HTO_IGO_11175_B_18_S18_L001_R2_001.fastq-004.gz", "fastq fastq", 6220719747.0, 51410907.0, "GSM5380072 r3", "0:29 1:92", "A:3158621534;C:796885709;G:1264774949;T:1000285734;N:151821", 29, 92, null, null, 3158621534, 796885709, 1264774949, 1000285734, 151821, "SRX11137027", "SRS9200152", "SRA1145723", "GEO", "Memorial Sloan Kettering Cancer Center", 2, 0.00012, 0.14112, 9e-05, 0.135, 0.99993, 0.99953, 0.33333, 0.55555, 29, 92, "T", "B", "sc-like readlen", "illumina", "novaseq_era", "unknown", "cdna_unspecified", "unknown", "sc", "single_cell_droplet", "10x", null, "United States", "2021-06-14", "Adult", "Adult", "Cancer or Tumor", "Cancer or Tumor"], [61557, "SRR14804254", "SRX11137027", "SRS9200152", "SRP287858", "PRJNA670235", "Spatially resolved transcriptomics reveals the architecture of the tumor microenvironment interface", "GSE159709", "Transcriptome Analysis", "Cancer cells interact with a wide variety of other cell types  but our understanding of microenvironmental heterogeneity and how it influences tumor phenotypes is limited. While single cell RNA seq scRNA seq has helped define these TME cell types  it provides limited information on the mechanisms that define how individual tumor cells interact with TME. Here  we integrate spatial transcriptomics with scRNA seq to define the architecture and nature of nascent tumor and surrounding microenvironment cells as they come into contact through the process of invasion. Using a well defined transgenic zebrafish model of BRAFV600E driven melanoma  we identify a transcriptionally unique \u201cinterface\u201d cluster localized at the boundary between tumor cells and surrounding tissues. Using an unbiased  data driven approach  we identify spatially patterned gene modules specific to the interface and show that the interface is a distinct transcriptional entity that histologically resembles the microenvironment but transcriptionally resembles the tumor. By complementing ST with scRNA seq  we demonstrate that the interface is composed of specialized tumor and microenvironment cells. Both cell types in the interface upregulate a common set of cilia genes  and we find enrichment of cilia proteins only where the tumor meets the TME. Cilia gene expression is regulated by ETS family transcription factors  which normally act to suppress their expression outside of this region. This unique ETS driven interface transcriptional state is conserved across ten different human patient samples  suggesting this is a conserved feature of human melanoma. Taken together  our results demonstrate the power of spatial and single cell transcriptomics techniques in uncovering novel biological mechanisms that drive tumor invasion into new tissues.  Overall design: Spatial transcriptomics Visium platform of zebrafish bearing BRAF V600E driven melanomas. Single cell RNA seq 10X Genomics v3 of two such zebrafish. Single nucleus RNA seq 10X Genomics v3 of three such zebrafish pooled into one reaction.", null, "pubmed:34725363", null, "Nuc seq", "GSM5380072", null, "tissue:Zebrafish melanomas BRAF V600E|sample type:Single nucleus suspension", "Nuc seq", "Illumina RTA v2 software was used for basecalling and quality determination. The 10x Genomics three prime v3 raw FASTQ data was processed using 10X Genomics proprietary CellRanger v5.0.1 pipeline. Genome build: GRCz10.88 Supplementary files format and content: For 10x Genomics three prime GEX v3 data: output of CellRanger pipeline including gene expression matrix  features and barcodes.", "Zebrafish melanomas BRAF V600E", null, "Adult tumor bearing fish were dissected to obtain only the tumor and surrounding tissues i.e head and tail were removed. The tissue was then ground in a Dounce homogenizer on ice in Nuclei EZ Prep Lysis Buffer Sigma Aldrich #NUC101. The nuclear suspension was then spun down at 4\u00b0C 500g  5 min. post resuspending the pellet in 1 mL wash buffer 250 mM sucrose  50 mM citric acid  1% BSA  20 mM DTT  0.2U/\u00b5L RNAse inhibitor  the sample was again spun at 4\u00b0C for 5 min at 500g. The pellet was resuspended in 1 mL wash buffer and subsequently sorted at 4\u00b0C to isolate individual nuclei  using a BD FACSAria III cell sorter BD Biosciences. Approximately equal numbers of GFP+ tumor and GFP  microenvironment nuclei were collected. Equal numbers of sorted GFP+ tumor and GFP  microenvironment nuclei were centrifuged at 600g for 5 minutes at 4\u00b0C. Droplet based snRNA seq was performed using the Chromium Single Cell 3\u2019 Library & Gel Bead Kit v3 10X Genomics and Chromium Single Cell 3\u2019 Chip G 10X Genomics. Approximately 12 000 nuclei were encapsulated in a single v3 reaction. GEM generation and library preparation were performed according to manufacturer\u2019s instructions.\u00a0", null, "sample type:Single nucleus suspension", "GSM5380072", "GSM5380072: Nuc seq; Danio rerio; RNA Seq", "GSM5380072", null, "1", "Adult tumor bearing fish were dissected to obtain only the tumor and surrounding tissues i.e head and tail were removed. The tissue was then ground in a Dounce homogenizer on ice in Nuclei EZ Prep Lysis Buffer Sigma Aldrich #NUC101. The nuclear suspension was then spun down at 4\u00b0C 500g  5 min. post resuspending the pellet in 1 mL wash buffer 250 mM sucrose  50 mM citric acid  1% BSA  20 mM DTT  0.2U/\u00b5L RNAse inhibitor  the sample was again spun at 4\u00b0C for 5 min at 500g. The pellet was resuspended in 1 mL wash buffer and subsequently sorted at 4\u00b0C to isolate individual nuclei  using a BD FACSAria III cell sorter BD Biosciences. Approximately equal numbers of GFP+ tumor and GFP  microenvironment nuclei were collected. Equal numbers of sorted GFP+ tumor and GFP  microenvironment nuclei were centrifuged at 600g for 5 minutes at 4\u00b0C. Droplet based snRNA seq was performed using the Chromium Single Cell three prime Library & Gel Bead Kit v3 10X Genomics and Chromium Single Cell three prime Chip G 10X Genomics. Approximately 12 000 nuclei were encapsulated in a single v3 reaction. GEM generation and library preparation were performed according to manufacturer's instructions.", "GEO Accession:GSM5380072", "RNA-Seq", "TRANSCRIPTOMIC", "cDNA", "PAIRED", "ILLUMINA", "Illumina NovaSeq 6000", null, "SRP287858", null, null, "2498_Zebrafish_HTO_IGO_11175_B_18_S18_L002_R1_001.fastq.gz 2498_Zebrafish_HTO_IGO_11175_B_18_S18_L002_R2_001.fastq-003.gz", "fastq fastq", 6140782307.0, 50750267.0, "GSM5380072 r4", "0:29 1:92", "A:3118957514;C:786290907;G:1248322710;T:987056069;N:155107", 29, 92, null, null, 3118957514, 786290907, 1248322710, 987056069, 155107, "SRX11137027", "SRS9200152", "SRA1145723", "GEO", "Memorial Sloan Kettering Cancer Center", 2, 0.00011, 0.13904, 9e-05, 0.13261, 0.99995, 0.99959, 1.0, 0.42857, 29, 92, "T", "B", "sc-like readlen", "illumina", "novaseq_era", "unknown", "cdna_unspecified", "unknown", "sc", "single_cell_droplet", "10x", null, "United States", "2021-06-14", "Adult", "Adult", "Cancer or Tumor", "Cancer or Tumor"], [61558, "SRR12851622", "SRX9318589", "SRS7543399", "SRP287858", "PRJNA670235", "Spatially resolved transcriptomics reveals the architecture of the tumor microenvironment interface", "GSE159709", "Transcriptome Analysis", "Cancer cells interact with a wide variety of other cell types  but our understanding of microenvironmental heterogeneity and how it influences tumor phenotypes is limited. While single cell RNA seq scRNA seq has helped define these TME cell types  it provides limited information on the mechanisms that define how individual tumor cells interact with TME. Here  we integrate spatial transcriptomics with scRNA seq to define the architecture and nature of nascent tumor and surrounding microenvironment cells as they come into contact through the process of invasion. Using a well defined transgenic zebrafish model of BRAFV600E driven melanoma  we identify a transcriptionally unique \u201cinterface\u201d cluster localized at the boundary between tumor cells and surrounding tissues. Using an unbiased  data driven approach  we identify spatially patterned gene modules specific to the interface and show that the interface is a distinct transcriptional entity that histologically resembles the microenvironment but transcriptionally resembles the tumor. By complementing ST with scRNA seq  we demonstrate that the interface is composed of specialized tumor and microenvironment cells. Both cell types in the interface upregulate a common set of cilia genes  and we find enrichment of cilia proteins only where the tumor meets the TME. Cilia gene expression is regulated by ETS family transcription factors  which normally act to suppress their expression outside of this region. This unique ETS driven interface transcriptional state is conserved across ten different human patient samples  suggesting this is a conserved feature of human melanoma. Taken together  our results demonstrate the power of spatial and single cell transcriptomics techniques in uncovering novel biological mechanisms that drive tumor invasion into new tissues.  Overall design: Spatial transcriptomics Visium platform of zebrafish bearing BRAF V600E driven melanomas. Single cell RNA seq 10X Genomics v3 of two such zebrafish. Single nucleus RNA seq 10X Genomics v3 of three such zebrafish pooled into one reaction.", null, "pubmed:34725363", null, "SingleCell F", "GSM4838135", null, "tissue:Zebrafish melanomas BRAF V600E|sample type:Single cell suspension", "SingleCell F", "Illumina RTA v2 software was used for basecalling and quality determination. The Visium raw FASTQ data was processed using 10X Genomics proprietary SpaceRanger v1.0.0 pipeline. The single cell RNA seq raw FASTQ data was processed using the 10X Genomics proprietary CellRanger v3.1.0 pipeline Genome build: GRCz10.88 Supplementary files format and content: For 10x Genomics spatial transcriptomic data: output of SpaceRanger pipeline  including gene expression and spatial contents. For 10x Genomics single cell RNA Seq: output of CellRanger pipeline  including gene expression  features and barcodes.", "Zebrafish melanomas BRAF V600E", null, "For spatial transcriptomics using the Visium platform from 10X genomics: Adult tumor bearing fish were euthanized on ice and washed in 1X PBS. post dissection of the head and tail  the remaining tissue was equilibrated in cold OCT for 2 minutes  before transfer to a tissue mold filled with fresh OCT for snap freezing in liquid nitrogen chilled isopentane. Tissue blocks were stored at  80\u00b0C. For cryosectioning  both the tissue block and the ST slide were equilibrated inside the cryostat for 15 30 minutes at 16\u00b0C before sectioning. Transverse sections through the entire fish were cut at a thickness of 10 \u00b5m and immediately placed on the ST slide Visium Spatial Gene Expression Slides  10X Genomics. ST slides containing sections were stored at  80\u00b0C for a maximum of one week before use. For single cell RNA seq using the 10X genomics 3\u2019 GEX v3 platform: Adult tumor bearing fish were dissected to obtain only the tumor and surrounding tissues i.e head and tail were removed. Tissue was minced with a fresh scalpel and incubated in 0.16 mg/mL liberase Sigma Aldrich #5401020001 in 0.9X PBS for 15 minutes at RT. Tissue was then further dissociated by repeated pipetting with a wide bore P1000  followed by incubation for an additional 15 minutes at RT. post adding 500 uL FBS to stop the dissociation reaction  samples were filtered through a 70 \u00b5m filter and centrifuged at 500g for 5 minutes at RT. The resulting pellet was resuspended in DMEM supplemented with 2% FBS  and cells were sorted at room temperature to remove debris and doublets  using a BD FACSAria III cell sorter BD Biosciences. Equal numbers of GFP+ tumor and GFP  macroenvironment cells were collected.\u00a0 For spatial transcriptomics using the Visium platform from 10X genomics: Samples were processed according to the Visium Spatial Gene Expression User Guide 10X Genomics and all reagents were from the Visium Spatial Gene Expression Kit 10X Genomics. Briefly  sections were fixed in chilled methanol for 30 min at  20\u00b0C  stained with hematoxylin and eosin  and mounted in 85% glycerol for imaging. Imaging was performed on a Leica SCN400 F whole slide scanner at 40X magnification. post imaging  sections were permeabilized at 37\u00b0C for 45 minutes. post permeabilization  the on slide reverse transcription RT reaction was performed at 53\u00b0C for 2 hours. Permeabilization time and RT reaction length were determined using the Visium Spatial Tissue Optimization Kit 10X Genomics. Second strand synthesis was subsequently performed on slide for 15 minutes at 65\u00b0C. All on slide reactions were performed in a thermocycler with a metal slide adaptor plate. Following second strand synthesis  samples were transferred to tubes for cDNA amplification and cleanup. Library quality was assayed using a Bioanalyzer High Sensitivity chip Agilent. For single cell RNA seq using the 10X genomics 3\u2019 GEX v3 platform: Equal numbers of sorted GFP+ tumor and GFP  macroenvironment cells were centrifuged at 300g for 5 minutes at RT  and resuspended in DMEM + 10% FBS. Droplet based scRNA seq was performed using the Chromium Single Cell 3\u2019 Library & Gel Bead Kit v3 10X Genomics and Chromium Single Cell 3\u2019 Chip G 10X Genomics. Approximately 10 000 cells from two fish were split encapsulated in a single v3 reaction. GEM generation and library preparation were performed according to manufacturer\u2019s instructions.", null, "sample type:Single cell suspension", "GSM4838135", "GSM4838135: SingleCell F; Danio rerio; RNA Seq", "GSM4838135", null, "1", "For spatial transcriptomics using the Visium platform from 10X genomics: Adult tumor bearing fish were euthanized on ice and washed in 1X PBS. post dissection of the head and tail  the remaining tissue was equilibrated in cold OCT for 2 minutes  before transfer to a tissue mold filled with fresh OCT for snap freezing in liquid nitrogen chilled isopentane. Tissue blocks were stored at  80\u00b0C. For cryosectioning  both the tissue block and the ST slide were equilibrated inside the cryostat for 15 30 minutes at 16\u00b0C before sectioning. Transverse sections through the entire fish were cut at a thickness of 10 \u00b5m and immediately placed on the ST slide Visium Spatial Gene Expression Slides  10X Genomics. ST slides containing sections were stored at  80\u00b0C for a maximum of one week before use. For single cell RNA seq using the 10X genomics three prime GEX v3 platform: Adult tumor bearing fish were dissected to obtain only the tumor and surrounding tissues i.e head and tail were removed. Tissue was minced with a fresh scalpel and incubated in 0.16 mg/mL liberase Sigma Aldrich #5401020001 in 0.9X PBS for 15 minutes at RT. Tissue was then further dissociated by repeated pipetting with a wide bore P1000  followed by incubation for an additional 15 minutes at RT. post adding 500 uL FBS to stop the dissociation reaction  samples were filtered through a 70 \u00b5m filter and centrifuged at 500g for 5 minutes at RT. The resulting pellet was resuspended in DMEM supplemented with 2% FBS  and cells were sorted at room temperature to remove debris and doublets  using a BD FACSAria III cell sorter BD Biosciences. Equal numbers of GFP+ tumor and GFP  macroenvironment cells were collected.  For spatial transcriptomics using the Visium platform from 10X genomics: Samples were processed according to the Visium Spatial Gene Expression User Guide 10X Genomics and all reagents were from the Visium Spatial Gene Expression Kit 10X Genomics. Briefly  sections were fixed in chilled methanol for 30 min at  20\u00b0C  stained with hematoxylin and eosin  and mounted in 85% glycerol for imaging. Imaging was performed on a Leica SCN400 F whole slide scanner at 40X magnification. post imaging  sections were permeabilized at 37\u00b0C for 45 minutes. post permeabilization  the on slide reverse transcription RT reaction was performed at 53\u00b0C for 2 hours. Permeabilization time and RT reaction length were determined using the Visium Spatial Tissue Optimization Kit 10X Genomics. Second strand synthesis was subsequently performed on slide for 15 minutes at 65\u00b0C. All on slide reactions were performed in a thermocycler with a metal slide adaptor plate. Following second strand synthesis  samples were transferred to tubes for cDNA amplification and cleanup. Library quality was assayed using a Bioanalyzer High Sensitivity chip Agilent. For single cell RNA seq using the 10X genomics three prime GEX v3 platform: Equal numbers of sorted GFP+ tumor and GFP  macroenvironment cells were centrifuged at 300g for 5 minutes at RT  and resuspended in DMEM + 10% FBS. Droplet based scRNA seq was performed using the Chromium Single Cell three prime Library & Gel Bead Kit v3 10X Genomics and Chromium Single Cell three prime Chip G 10X Genomics. Approximately 10 000 cells from two fish were split encapsulated in a single v3 reaction. GEM generation and library preparation were performed according to manufacturer's instructions.", "GEO Accession:GSM4838135", "RNA-Seq", "TRANSCRIPTOMIC", "cDNA", "PAIRED", "ILLUMINA", "NextSeq 500", null, "SRP287858", null, null, "10X_SingleCell_Sample_F_S1_L000_R1_001.fastq.gz 10X_SingleCell_Sample_F_S1_L000_R2_001.fastq.gz", "fastq fastq", 44547263840.0, 278420399.0, "GSM4838135 r1", "0:28 1:132", "A:12810925700;C:9421837786;G:9930050611;T:12378989254;N:5460489", 28, 132, null, null, 12810925700, 9421837786, 9930050611, 12378989254, 5460489, "SRX9318589", "SRS7543399", "SRA1145723", "GEO", "Memorial Sloan Kettering Cancer Center", 2, 0.00339, 0.91854, 0.00135, 0.1624, 0.99494, 0.79744, 0.35078, 0.56648, 28, 132, "T", "B", "sc-like readlen", "illumina", "nextseq", "unknown", "random_priming", "unknown", "sc", "single_cell_droplet", "10x", null, "United States", "2020-10-20", "Adult", "Adult", "Cancer or Tumor", "Cancer or Tumor"], [61559, "SRR12851621", "SRX9318588", "SRS7543398", "SRP287858", "PRJNA670235", "Spatially resolved transcriptomics reveals the architecture of the tumor microenvironment interface", "GSE159709", "Transcriptome Analysis", "Cancer cells interact with a wide variety of other cell types  but our understanding of microenvironmental heterogeneity and how it influences tumor phenotypes is limited. While single cell RNA seq scRNA seq has helped define these TME cell types  it provides limited information on the mechanisms that define how individual tumor cells interact with TME. Here  we integrate spatial transcriptomics with scRNA seq to define the architecture and nature of nascent tumor and surrounding microenvironment cells as they come into contact through the process of invasion. Using a well defined transgenic zebrafish model of BRAFV600E driven melanoma  we identify a transcriptionally unique \u201cinterface\u201d cluster localized at the boundary between tumor cells and surrounding tissues. Using an unbiased  data driven approach  we identify spatially patterned gene modules specific to the interface and show that the interface is a distinct transcriptional entity that histologically resembles the microenvironment but transcriptionally resembles the tumor. By complementing ST with scRNA seq  we demonstrate that the interface is composed of specialized tumor and microenvironment cells. Both cell types in the interface upregulate a common set of cilia genes  and we find enrichment of cilia proteins only where the tumor meets the TME. Cilia gene expression is regulated by ETS family transcription factors  which normally act to suppress their expression outside of this region. This unique ETS driven interface transcriptional state is conserved across ten different human patient samples  suggesting this is a conserved feature of human melanoma. Taken together  our results demonstrate the power of spatial and single cell transcriptomics techniques in uncovering novel biological mechanisms that drive tumor invasion into new tissues.  Overall design: Spatial transcriptomics Visium platform of zebrafish bearing BRAF V600E driven melanomas. Single cell RNA seq 10X Genomics v3 of two such zebrafish. Single nucleus RNA seq 10X Genomics v3 of three such zebrafish pooled into one reaction.", null, "pubmed:34725363", null, "SingleCell E", "GSM4838134", null, "tissue:Zebrafish melanomas BRAF V600E|sample type:Single cell suspension", "SingleCell E", "Illumina RTA v2 software was used for basecalling and quality determination. The Visium raw FASTQ data was processed using 10X Genomics proprietary SpaceRanger v1.0.0 pipeline. The single cell RNA seq raw FASTQ data was processed using the 10X Genomics proprietary CellRanger v3.1.0 pipeline Genome build: GRCz10.88 Supplementary files format and content: For 10x Genomics spatial transcriptomic data: output of SpaceRanger pipeline  including gene expression and spatial contents. For 10x Genomics single cell RNA Seq: output of CellRanger pipeline  including gene expression  features and barcodes.", "Zebrafish melanomas BRAF V600E", null, "For spatial transcriptomics using the Visium platform from 10X genomics: Adult tumor bearing fish were euthanized on ice and washed in 1X PBS. post dissection of the head and tail  the remaining tissue was equilibrated in cold OCT for 2 minutes  before transfer to a tissue mold filled with fresh OCT for snap freezing in liquid nitrogen chilled isopentane. Tissue blocks were stored at  80\u00b0C. For cryosectioning  both the tissue block and the ST slide were equilibrated inside the cryostat for 15 30 minutes at 16\u00b0C before sectioning. Transverse sections through the entire fish were cut at a thickness of 10 \u00b5m and immediately placed on the ST slide Visium Spatial Gene Expression Slides  10X Genomics. ST slides containing sections were stored at  80\u00b0C for a maximum of one week before use. For single cell RNA seq using the 10X genomics 3\u2019 GEX v3 platform: Adult tumor bearing fish were dissected to obtain only the tumor and surrounding tissues i.e head and tail were removed. Tissue was minced with a fresh scalpel and incubated in 0.16 mg/mL liberase Sigma Aldrich #5401020001 in 0.9X PBS for 15 minutes at RT. Tissue was then further dissociated by repeated pipetting with a wide bore P1000  followed by incubation for an additional 15 minutes at RT. post adding 500 uL FBS to stop the dissociation reaction  samples were filtered through a 70 \u00b5m filter and centrifuged at 500g for 5 minutes at RT. The resulting pellet was resuspended in DMEM supplemented with 2% FBS  and cells were sorted at room temperature to remove debris and doublets  using a BD FACSAria III cell sorter BD Biosciences. Equal numbers of GFP+ tumor and GFP  macroenvironment cells were collected.\u00a0 For spatial transcriptomics using the Visium platform from 10X genomics: Samples were processed according to the Visium Spatial Gene Expression User Guide 10X Genomics and all reagents were from the Visium Spatial Gene Expression Kit 10X Genomics. Briefly  sections were fixed in chilled methanol for 30 min at  20\u00b0C  stained with hematoxylin and eosin  and mounted in 85% glycerol for imaging. Imaging was performed on a Leica SCN400 F whole slide scanner at 40X magnification. post imaging  sections were permeabilized at 37\u00b0C for 45 minutes. post permeabilization  the on slide reverse transcription RT reaction was performed at 53\u00b0C for 2 hours. Permeabilization time and RT reaction length were determined using the Visium Spatial Tissue Optimization Kit 10X Genomics. Second strand synthesis was subsequently performed on slide for 15 minutes at 65\u00b0C. All on slide reactions were performed in a thermocycler with a metal slide adaptor plate. Following second strand synthesis  samples were transferred to tubes for cDNA amplification and cleanup. Library quality was assayed using a Bioanalyzer High Sensitivity chip Agilent. For single cell RNA seq using the 10X genomics 3\u2019 GEX v3 platform: Equal numbers of sorted GFP+ tumor and GFP  macroenvironment cells were centrifuged at 300g for 5 minutes at RT  and resuspended in DMEM + 10% FBS. Droplet based scRNA seq was performed using the Chromium Single Cell 3\u2019 Library & Gel Bead Kit v3 10X Genomics and Chromium Single Cell 3\u2019 Chip G 10X Genomics. Approximately 10 000 cells from two fish were split encapsulated in a single v3 reaction. GEM generation and library preparation were performed according to manufacturer\u2019s instructions.", null, "sample type:Single cell suspension", "GSM4838134", "GSM4838134: SingleCell E; Danio rerio; RNA Seq", "GSM4838134", null, "1", "For spatial transcriptomics using the Visium platform from 10X genomics: Adult tumor bearing fish were euthanized on ice and washed in 1X PBS. post dissection of the head and tail  the remaining tissue was equilibrated in cold OCT for 2 minutes  before transfer to a tissue mold filled with fresh OCT for snap freezing in liquid nitrogen chilled isopentane. Tissue blocks were stored at  80\u00b0C. For cryosectioning  both the tissue block and the ST slide were equilibrated inside the cryostat for 15 30 minutes at 16\u00b0C before sectioning. Transverse sections through the entire fish were cut at a thickness of 10 \u00b5m and immediately placed on the ST slide Visium Spatial Gene Expression Slides  10X Genomics. ST slides containing sections were stored at  80\u00b0C for a maximum of one week before use. For single cell RNA seq using the 10X genomics three prime GEX v3 platform: Adult tumor bearing fish were dissected to obtain only the tumor and surrounding tissues i.e head and tail were removed. Tissue was minced with a fresh scalpel and incubated in 0.16 mg/mL liberase Sigma Aldrich #5401020001 in 0.9X PBS for 15 minutes at RT. Tissue was then further dissociated by repeated pipetting with a wide bore P1000  followed by incubation for an additional 15 minutes at RT. post adding 500 uL FBS to stop the dissociation reaction  samples were filtered through a 70 \u00b5m filter and centrifuged at 500g for 5 minutes at RT. The resulting pellet was resuspended in DMEM supplemented with 2% FBS  and cells were sorted at room temperature to remove debris and doublets  using a BD FACSAria III cell sorter BD Biosciences. Equal numbers of GFP+ tumor and GFP  macroenvironment cells were collected.  For spatial transcriptomics using the Visium platform from 10X genomics: Samples were processed according to the Visium Spatial Gene Expression User Guide 10X Genomics and all reagents were from the Visium Spatial Gene Expression Kit 10X Genomics. Briefly  sections were fixed in chilled methanol for 30 min at  20\u00b0C  stained with hematoxylin and eosin  and mounted in 85% glycerol for imaging. Imaging was performed on a Leica SCN400 F whole slide scanner at 40X magnification. post imaging  sections were permeabilized at 37\u00b0C for 45 minutes. post permeabilization  the on slide reverse transcription RT reaction was performed at 53\u00b0C for 2 hours. Permeabilization time and RT reaction length were determined using the Visium Spatial Tissue Optimization Kit 10X Genomics. Second strand synthesis was subsequently performed on slide for 15 minutes at 65\u00b0C. All on slide reactions were performed in a thermocycler with a metal slide adaptor plate. Following second strand synthesis  samples were transferred to tubes for cDNA amplification and cleanup. Library quality was assayed using a Bioanalyzer High Sensitivity chip Agilent. For single cell RNA seq using the 10X genomics three prime GEX v3 platform: Equal numbers of sorted GFP+ tumor and GFP  macroenvironment cells were centrifuged at 300g for 5 minutes at RT  and resuspended in DMEM + 10% FBS. Droplet based scRNA seq was performed using the Chromium Single Cell three prime Library & Gel Bead Kit v3 10X Genomics and Chromium Single Cell three prime Chip G 10X Genomics. Approximately 10 000 cells from two fish were split encapsulated in a single v3 reaction. GEM generation and library preparation were performed according to manufacturer's instructions.", "GEO Accession:GSM4838134", "RNA-Seq", "TRANSCRIPTOMIC", "cDNA", "PAIRED", "ILLUMINA", "NextSeq 500", null, "SRP287858", null, null, "10X_SingleCell_Sample_E_S1_L000_R1_001.fastq.gz 10X_SingleCell_Sample_E_S1_L000_R2_001.fastq.gz", "fastq fastq", 44430354080.0, 277689713.0, "GSM4838134 r1", "0:28 1:132", "A:12355044923;C:9923404810;G:10323616312;T:11822807950;N:5480085", 28, 132, null, null, 12355044923, 9923404810, 10323616312, 11822807950, 5480085, "SRX9318588", "SRS7543398", "SRA1145723", "GEO", "Memorial Sloan Kettering Cancer Center", 2, 0.00204, 0.9315, 0.00092, 0.09404, 0.9964, 0.83027, 0.40865, 0.54937, 28, 132, "T", "B", "sc-like readlen", "illumina", "nextseq", "unknown", "random_priming", "unknown", "sc", "single_cell_droplet", "10x", null, "United States", "2020-10-20", "Adult", "Adult", "Cancer or Tumor", "Cancer or Tumor"], [61560, "SRR12851620", "SRX9318587", "SRS7543397", "SRP287858", "PRJNA670235", "Spatially resolved transcriptomics reveals the architecture of the tumor microenvironment interface", "GSE159709", "Transcriptome Analysis", "Cancer cells interact with a wide variety of other cell types  but our understanding of microenvironmental heterogeneity and how it influences tumor phenotypes is limited. While single cell RNA seq scRNA seq has helped define these TME cell types  it provides limited information on the mechanisms that define how individual tumor cells interact with TME. Here  we integrate spatial transcriptomics with scRNA seq to define the architecture and nature of nascent tumor and surrounding microenvironment cells as they come into contact through the process of invasion. Using a well defined transgenic zebrafish model of BRAFV600E driven melanoma  we identify a transcriptionally unique \u201cinterface\u201d cluster localized at the boundary between tumor cells and surrounding tissues. Using an unbiased  data driven approach  we identify spatially patterned gene modules specific to the interface and show that the interface is a distinct transcriptional entity that histologically resembles the microenvironment but transcriptionally resembles the tumor. By complementing ST with scRNA seq  we demonstrate that the interface is composed of specialized tumor and microenvironment cells. Both cell types in the interface upregulate a common set of cilia genes  and we find enrichment of cilia proteins only where the tumor meets the TME. Cilia gene expression is regulated by ETS family transcription factors  which normally act to suppress their expression outside of this region. This unique ETS driven interface transcriptional state is conserved across ten different human patient samples  suggesting this is a conserved feature of human melanoma. Taken together  our results demonstrate the power of spatial and single cell transcriptomics techniques in uncovering novel biological mechanisms that drive tumor invasion into new tissues.  Overall design: Spatial transcriptomics Visium platform of zebrafish bearing BRAF V600E driven melanomas. Single cell RNA seq 10X Genomics v3 of two such zebrafish. Single nucleus RNA seq 10X Genomics v3 of three such zebrafish pooled into one reaction.", null, "pubmed:34725363", null, "Visium C", "GSM4838133", null, "tissue:Zebrafish melanomas BRAF V600E|sample type:Tissue cryosections", "Visium C", "Illumina RTA v2 software was used for basecalling and quality determination. The Visium raw FASTQ data was processed using 10X Genomics proprietary SpaceRanger v1.0.0 pipeline. The single cell RNA seq raw FASTQ data was processed using the 10X Genomics proprietary CellRanger v3.1.0 pipeline Genome build: GRCz10.88 Supplementary files format and content: For 10x Genomics spatial transcriptomic data: output of SpaceRanger pipeline  including gene expression and spatial contents. For 10x Genomics single cell RNA Seq: output of CellRanger pipeline  including gene expression  features and barcodes. Supplementary files format and content: * image.tif: Tissue section used for Spatial Transcriptomics experiment.", "Zebrafish melanomas BRAF V600E", null, "For spatial transcriptomics using the Visium platform from 10X genomics: Adult tumor bearing fish were euthanized on ice and washed in 1X PBS. post dissection of the head and tail  the remaining tissue was equilibrated in cold OCT for 2 minutes  before transfer to a tissue mold filled with fresh OCT for snap freezing in liquid nitrogen chilled isopentane. Tissue blocks were stored at  80\u00b0C. For cryosectioning  both the tissue block and the ST slide were equilibrated inside the cryostat for 15 30 minutes at 16\u00b0C before sectioning. Transverse sections through the entire fish were cut at a thickness of 10 \u00b5m and immediately placed on the ST slide Visium Spatial Gene Expression Slides  10X Genomics. ST slides containing sections were stored at  80\u00b0C for a maximum of one week before use. For single cell RNA seq using the 10X genomics 3\u2019 GEX v3 platform: Adult tumor bearing fish were dissected to obtain only the tumor and surrounding tissues i.e head and tail were removed. Tissue was minced with a fresh scalpel and incubated in 0.16 mg/mL liberase Sigma Aldrich #5401020001 in 0.9X PBS for 15 minutes at RT. Tissue was then further dissociated by repeated pipetting with a wide bore P1000  followed by incubation for an additional 15 minutes at RT. post adding 500 uL FBS to stop the dissociation reaction  samples were filtered through a 70 \u00b5m filter and centrifuged at 500g for 5 minutes at RT. The resulting pellet was resuspended in DMEM supplemented with 2% FBS  and cells were sorted at room temperature to remove debris and doublets  using a BD FACSAria III cell sorter BD Biosciences. Equal numbers of GFP+ tumor and GFP  macroenvironment cells were collected.\u00a0 For spatial transcriptomics using the Visium platform from 10X genomics: Samples were processed according to the Visium Spatial Gene Expression User Guide 10X Genomics and all reagents were from the Visium Spatial Gene Expression Kit 10X Genomics. Briefly  sections were fixed in chilled methanol for 30 min at  20\u00b0C  stained with hematoxylin and eosin  and mounted in 85% glycerol for imaging. Imaging was performed on a Leica SCN400 F whole slide scanner at 40X magnification. post imaging  sections were permeabilized at 37\u00b0C for 45 minutes. post permeabilization  the on slide reverse transcription RT reaction was performed at 53\u00b0C for 2 hours. Permeabilization time and RT reaction length were determined using the Visium Spatial Tissue Optimization Kit 10X Genomics. Second strand synthesis was subsequently performed on slide for 15 minutes at 65\u00b0C. All on slide reactions were performed in a thermocycler with a metal slide adaptor plate. Following second strand synthesis  samples were transferred to tubes for cDNA amplification and cleanup. Library quality was assayed using a Bioanalyzer High Sensitivity chip Agilent. For single cell RNA seq using the 10X genomics 3\u2019 GEX v3 platform: Equal numbers of sorted GFP+ tumor and GFP  macroenvironment cells were centrifuged at 300g for 5 minutes at RT  and resuspended in DMEM + 10% FBS. Droplet based scRNA seq was performed using the Chromium Single Cell 3\u2019 Library & Gel Bead Kit v3 10X Genomics and Chromium Single Cell 3\u2019 Chip G 10X Genomics. Approximately 10 000 cells from two fish were split encapsulated in a single v3 reaction. GEM generation and library preparation were performed according to manufacturer\u2019s instructions.", null, "sample type:Tissue cryosections", "GSM4838133", "GSM4838133: Visium C; Danio rerio; RNA Seq", "GSM4838133", null, "1", "For spatial transcriptomics using the Visium platform from 10X genomics: Adult tumor bearing fish were euthanized on ice and washed in 1X PBS. post dissection of the head and tail  the remaining tissue was equilibrated in cold OCT for 2 minutes  before transfer to a tissue mold filled with fresh OCT for snap freezing in liquid nitrogen chilled isopentane. Tissue blocks were stored at  80\u00b0C. For cryosectioning  both the tissue block and the ST slide were equilibrated inside the cryostat for 15 30 minutes at 16\u00b0C before sectioning. Transverse sections through the entire fish were cut at a thickness of 10 \u00b5m and immediately placed on the ST slide Visium Spatial Gene Expression Slides  10X Genomics. ST slides containing sections were stored at  80\u00b0C for a maximum of one week before use. For single cell RNA seq using the 10X genomics three prime GEX v3 platform: Adult tumor bearing fish were dissected to obtain only the tumor and surrounding tissues i.e head and tail were removed. Tissue was minced with a fresh scalpel and incubated in 0.16 mg/mL liberase Sigma Aldrich #5401020001 in 0.9X PBS for 15 minutes at RT. Tissue was then further dissociated by repeated pipetting with a wide bore P1000  followed by incubation for an additional 15 minutes at RT. post adding 500 uL FBS to stop the dissociation reaction  samples were filtered through a 70 \u00b5m filter and centrifuged at 500g for 5 minutes at RT. The resulting pellet was resuspended in DMEM supplemented with 2% FBS  and cells were sorted at room temperature to remove debris and doublets  using a BD FACSAria III cell sorter BD Biosciences. Equal numbers of GFP+ tumor and GFP  macroenvironment cells were collected.  For spatial transcriptomics using the Visium platform from 10X genomics: Samples were processed according to the Visium Spatial Gene Expression User Guide 10X Genomics and all reagents were from the Visium Spatial Gene Expression Kit 10X Genomics. Briefly  sections were fixed in chilled methanol for 30 min at  20\u00b0C  stained with hematoxylin and eosin  and mounted in 85% glycerol for imaging. Imaging was performed on a Leica SCN400 F whole slide scanner at 40X magnification. post imaging  sections were permeabilized at 37\u00b0C for 45 minutes. post permeabilization  the on slide reverse transcription RT reaction was performed at 53\u00b0C for 2 hours. Permeabilization time and RT reaction length were determined using the Visium Spatial Tissue Optimization Kit 10X Genomics. Second strand synthesis was subsequently performed on slide for 15 minutes at 65\u00b0C. All on slide reactions were performed in a thermocycler with a metal slide adaptor plate. Following second strand synthesis  samples were transferred to tubes for cDNA amplification and cleanup. Library quality was assayed using a Bioanalyzer High Sensitivity chip Agilent. For single cell RNA seq using the 10X genomics three prime GEX v3 platform: Equal numbers of sorted GFP+ tumor and GFP  macroenvironment cells were centrifuged at 300g for 5 minutes at RT  and resuspended in DMEM + 10% FBS. Droplet based scRNA seq was performed using the Chromium Single Cell three prime Library & Gel Bead Kit v3 10X Genomics and Chromium Single Cell three prime Chip G 10X Genomics. Approximately 10 000 cells from two fish were split encapsulated in a single v3 reaction. GEM generation and library preparation were performed according to manufacturer's instructions.", "GEO Accession:GSM4838133", "RNA-Seq", "TRANSCRIPTOMIC", "cDNA", "PAIRED", "ILLUMINA", "NextSeq 500", null, "SRP287858", null, null, "Visium_Sample_C_S3_L000_R1_001.fastq.gz Visium_Sample_C_S3_L000_R2_001.fastq.gz", "fastq fastq", 13306156376.0, 89906462.0, "GSM4838133 r1", "0:28 1:120", "A:4587866955;C:2519579655;G:2801896206;T:3387510435;N:9303125", 28, 120, null, null, 4587866955, 2519579655, 2801896206, 3387510435, 9303125, "SRX9318587", "SRS7543397", "SRA1145723", "GEO", "Memorial Sloan Kettering Cancer Center", 2, 0.0035, 0.64737, 0.00263, 0.05262, 0.99734, 0.91959, 0.55029, 0.53722, 28, 120, "T", "B", "sc-like readlen", "illumina", "nextseq", "unknown", "random_priming", "unknown", "sc", "single_cell_droplet", "10x", null, "United States", "2020-10-20", "Adult", "Adult", "Cancer or Tumor", "Cancer or Tumor"], [61561, "SRR12851619", "SRX9318586", "SRS7543396", "SRP287858", "PRJNA670235", "Spatially resolved transcriptomics reveals the architecture of the tumor microenvironment interface", "GSE159709", "Transcriptome Analysis", "Cancer cells interact with a wide variety of other cell types  but our understanding of microenvironmental heterogeneity and how it influences tumor phenotypes is limited. While single cell RNA seq scRNA seq has helped define these TME cell types  it provides limited information on the mechanisms that define how individual tumor cells interact with TME. Here  we integrate spatial transcriptomics with scRNA seq to define the architecture and nature of nascent tumor and surrounding microenvironment cells as they come into contact through the process of invasion. Using a well defined transgenic zebrafish model of BRAFV600E driven melanoma  we identify a transcriptionally unique \u201cinterface\u201d cluster localized at the boundary between tumor cells and surrounding tissues. Using an unbiased  data driven approach  we identify spatially patterned gene modules specific to the interface and show that the interface is a distinct transcriptional entity that histologically resembles the microenvironment but transcriptionally resembles the tumor. By complementing ST with scRNA seq  we demonstrate that the interface is composed of specialized tumor and microenvironment cells. Both cell types in the interface upregulate a common set of cilia genes  and we find enrichment of cilia proteins only where the tumor meets the TME. Cilia gene expression is regulated by ETS family transcription factors  which normally act to suppress their expression outside of this region. This unique ETS driven interface transcriptional state is conserved across ten different human patient samples  suggesting this is a conserved feature of human melanoma. Taken together  our results demonstrate the power of spatial and single cell transcriptomics techniques in uncovering novel biological mechanisms that drive tumor invasion into new tissues.  Overall design: Spatial transcriptomics Visium platform of zebrafish bearing BRAF V600E driven melanomas. Single cell RNA seq 10X Genomics v3 of two such zebrafish. Single nucleus RNA seq 10X Genomics v3 of three such zebrafish pooled into one reaction.", null, "pubmed:34725363", null, "Visium B", "GSM4838132", null, "tissue:Zebrafish melanomas BRAF V600E|sample type:Tissue cryosections", "Visium B", "Illumina RTA v2 software was used for basecalling and quality determination. The Visium raw FASTQ data was processed using 10X Genomics proprietary SpaceRanger v1.0.0 pipeline. The single cell RNA seq raw FASTQ data was processed using the 10X Genomics proprietary CellRanger v3.1.0 pipeline Genome build: GRCz10.88 Supplementary files format and content: For 10x Genomics spatial transcriptomic data: output of SpaceRanger pipeline  including gene expression and spatial contents. For 10x Genomics single cell RNA Seq: output of CellRanger pipeline  including gene expression  features and barcodes. Supplementary files format and content: * image.tif: Tissue section used for Spatial Transcriptomics experiment.", "Zebrafish melanomas BRAF V600E", null, "For spatial transcriptomics using the Visium platform from 10X genomics: Adult tumor bearing fish were euthanized on ice and washed in 1X PBS. post dissection of the head and tail  the remaining tissue was equilibrated in cold OCT for 2 minutes  before transfer to a tissue mold filled with fresh OCT for snap freezing in liquid nitrogen chilled isopentane. Tissue blocks were stored at  80\u00b0C. For cryosectioning  both the tissue block and the ST slide were equilibrated inside the cryostat for 15 30 minutes at 16\u00b0C before sectioning. Transverse sections through the entire fish were cut at a thickness of 10 \u00b5m and immediately placed on the ST slide Visium Spatial Gene Expression Slides  10X Genomics. ST slides containing sections were stored at  80\u00b0C for a maximum of one week before use. For single cell RNA seq using the 10X genomics 3\u2019 GEX v3 platform: Adult tumor bearing fish were dissected to obtain only the tumor and surrounding tissues i.e head and tail were removed. Tissue was minced with a fresh scalpel and incubated in 0.16 mg/mL liberase Sigma Aldrich #5401020001 in 0.9X PBS for 15 minutes at RT. Tissue was then further dissociated by repeated pipetting with a wide bore P1000  followed by incubation for an additional 15 minutes at RT. post adding 500 uL FBS to stop the dissociation reaction  samples were filtered through a 70 \u00b5m filter and centrifuged at 500g for 5 minutes at RT. The resulting pellet was resuspended in DMEM supplemented with 2% FBS  and cells were sorted at room temperature to remove debris and doublets  using a BD FACSAria III cell sorter BD Biosciences. Equal numbers of GFP+ tumor and GFP  macroenvironment cells were collected.\u00a0 For spatial transcriptomics using the Visium platform from 10X genomics: Samples were processed according to the Visium Spatial Gene Expression User Guide 10X Genomics and all reagents were from the Visium Spatial Gene Expression Kit 10X Genomics. Briefly  sections were fixed in chilled methanol for 30 min at  20\u00b0C  stained with hematoxylin and eosin  and mounted in 85% glycerol for imaging. Imaging was performed on a Leica SCN400 F whole slide scanner at 40X magnification. post imaging  sections were permeabilized at 37\u00b0C for 45 minutes. post permeabilization  the on slide reverse transcription RT reaction was performed at 53\u00b0C for 2 hours. Permeabilization time and RT reaction length were determined using the Visium Spatial Tissue Optimization Kit 10X Genomics. Second strand synthesis was subsequently performed on slide for 15 minutes at 65\u00b0C. All on slide reactions were performed in a thermocycler with a metal slide adaptor plate. Following second strand synthesis  samples were transferred to tubes for cDNA amplification and cleanup. Library quality was assayed using a Bioanalyzer High Sensitivity chip Agilent. For single cell RNA seq using the 10X genomics 3\u2019 GEX v3 platform: Equal numbers of sorted GFP+ tumor and GFP  macroenvironment cells were centrifuged at 300g for 5 minutes at RT  and resuspended in DMEM + 10% FBS. Droplet based scRNA seq was performed using the Chromium Single Cell 3\u2019 Library & Gel Bead Kit v3 10X Genomics and Chromium Single Cell 3\u2019 Chip G 10X Genomics. Approximately 10 000 cells from two fish were split encapsulated in a single v3 reaction. GEM generation and library preparation were performed according to manufacturer\u2019s instructions.", null, "sample type:Tissue cryosections", "GSM4838132", "GSM4838132: Visium B; Danio rerio; RNA Seq", "GSM4838132", null, "1", "For spatial transcriptomics using the Visium platform from 10X genomics: Adult tumor bearing fish were euthanized on ice and washed in 1X PBS. post dissection of the head and tail  the remaining tissue was equilibrated in cold OCT for 2 minutes  before transfer to a tissue mold filled with fresh OCT for snap freezing in liquid nitrogen chilled isopentane. Tissue blocks were stored at  80\u00b0C. For cryosectioning  both the tissue block and the ST slide were equilibrated inside the cryostat for 15 30 minutes at 16\u00b0C before sectioning. Transverse sections through the entire fish were cut at a thickness of 10 \u00b5m and immediately placed on the ST slide Visium Spatial Gene Expression Slides  10X Genomics. ST slides containing sections were stored at  80\u00b0C for a maximum of one week before use. For single cell RNA seq using the 10X genomics three prime GEX v3 platform: Adult tumor bearing fish were dissected to obtain only the tumor and surrounding tissues i.e head and tail were removed. Tissue was minced with a fresh scalpel and incubated in 0.16 mg/mL liberase Sigma Aldrich #5401020001 in 0.9X PBS for 15 minutes at RT. Tissue was then further dissociated by repeated pipetting with a wide bore P1000  followed by incubation for an additional 15 minutes at RT. post adding 500 uL FBS to stop the dissociation reaction  samples were filtered through a 70 \u00b5m filter and centrifuged at 500g for 5 minutes at RT. The resulting pellet was resuspended in DMEM supplemented with 2% FBS  and cells were sorted at room temperature to remove debris and doublets  using a BD FACSAria III cell sorter BD Biosciences. Equal numbers of GFP+ tumor and GFP  macroenvironment cells were collected.  For spatial transcriptomics using the Visium platform from 10X genomics: Samples were processed according to the Visium Spatial Gene Expression User Guide 10X Genomics and all reagents were from the Visium Spatial Gene Expression Kit 10X Genomics. Briefly  sections were fixed in chilled methanol for 30 min at  20\u00b0C  stained with hematoxylin and eosin  and mounted in 85% glycerol for imaging. Imaging was performed on a Leica SCN400 F whole slide scanner at 40X magnification. post imaging  sections were permeabilized at 37\u00b0C for 45 minutes. post permeabilization  the on slide reverse transcription RT reaction was performed at 53\u00b0C for 2 hours. Permeabilization time and RT reaction length were determined using the Visium Spatial Tissue Optimization Kit 10X Genomics. Second strand synthesis was subsequently performed on slide for 15 minutes at 65\u00b0C. All on slide reactions were performed in a thermocycler with a metal slide adaptor plate. Following second strand synthesis  samples were transferred to tubes for cDNA amplification and cleanup. Library quality was assayed using a Bioanalyzer High Sensitivity chip Agilent. For single cell RNA seq using the 10X genomics three prime GEX v3 platform: Equal numbers of sorted GFP+ tumor and GFP  macroenvironment cells were centrifuged at 300g for 5 minutes at RT  and resuspended in DMEM + 10% FBS. Droplet based scRNA seq was performed using the Chromium Single Cell three prime Library & Gel Bead Kit v3 10X Genomics and Chromium Single Cell three prime Chip G 10X Genomics. Approximately 10 000 cells from two fish were split encapsulated in a single v3 reaction. GEM generation and library preparation were performed according to manufacturer's instructions.", "GEO Accession:GSM4838132", "RNA-Seq", "TRANSCRIPTOMIC", "cDNA", "PAIRED", "ILLUMINA", "NextSeq 500", null, "SRP287858", null, null, "Visium_Sample_B_S2_L000_R2_001.fastq.gz Visium_Sample_B_S2_L000_R1_001.fastq.gz", "fastq fastq", 9316849676.0, 62951687.0, "GSM4838132 r1", "0:28 1:120", "A:2870712770;C:1917570201;G:2077620827;T:2444412876;N:6533002", 28, 120, null, null, 2870712770, 1917570201, 2077620827, 2444412876, 6533002, "SRX9318586", "SRS7543396", "SRA1145723", "GEO", "Memorial Sloan Kettering Cancer Center", 2, 0.00194, 0.80482, 0.00091, 0.06131, 0.99711, 0.90325, 0.5736, 0.52314, 28, 120, "T", "B", "sc-like readlen", "illumina", "nextseq", "unknown", "random_priming", "unknown", "sc", "single_cell_droplet", "10x", null, "United States", "2020-10-20", "Adult", "Adult", "Cancer or Tumor", "Cancer or Tumor"], [61562, "SRR12851618", "SRX9318585", "SRS7543395", "SRP287858", "PRJNA670235", "Spatially resolved transcriptomics reveals the architecture of the tumor microenvironment interface", "GSE159709", "Transcriptome Analysis", "Cancer cells interact with a wide variety of other cell types  but our understanding of microenvironmental heterogeneity and how it influences tumor phenotypes is limited. While single cell RNA seq scRNA seq has helped define these TME cell types  it provides limited information on the mechanisms that define how individual tumor cells interact with TME. Here  we integrate spatial transcriptomics with scRNA seq to define the architecture and nature of nascent tumor and surrounding microenvironment cells as they come into contact through the process of invasion. Using a well defined transgenic zebrafish model of BRAFV600E driven melanoma  we identify a transcriptionally unique \u201cinterface\u201d cluster localized at the boundary between tumor cells and surrounding tissues. Using an unbiased  data driven approach  we identify spatially patterned gene modules specific to the interface and show that the interface is a distinct transcriptional entity that histologically resembles the microenvironment but transcriptionally resembles the tumor. By complementing ST with scRNA seq  we demonstrate that the interface is composed of specialized tumor and microenvironment cells. Both cell types in the interface upregulate a common set of cilia genes  and we find enrichment of cilia proteins only where the tumor meets the TME. Cilia gene expression is regulated by ETS family transcription factors  which normally act to suppress their expression outside of this region. This unique ETS driven interface transcriptional state is conserved across ten different human patient samples  suggesting this is a conserved feature of human melanoma. Taken together  our results demonstrate the power of spatial and single cell transcriptomics techniques in uncovering novel biological mechanisms that drive tumor invasion into new tissues.  Overall design: Spatial transcriptomics Visium platform of zebrafish bearing BRAF V600E driven melanomas. Single cell RNA seq 10X Genomics v3 of two such zebrafish. Single nucleus RNA seq 10X Genomics v3 of three such zebrafish pooled into one reaction.", null, "pubmed:34725363", null, "Visium A", "GSM4838131", null, "tissue:Zebrafish melanomas BRAF V600E|sample type:Tissue cryosections", "Visium A", "Illumina RTA v2 software was used for basecalling and quality determination. The Visium raw FASTQ data was processed using 10X Genomics proprietary SpaceRanger v1.0.0 pipeline. The single cell RNA seq raw FASTQ data was processed using the 10X Genomics proprietary CellRanger v3.1.0 pipeline Genome build: GRCz10.88 Supplementary files format and content: For 10x Genomics spatial transcriptomic data: output of SpaceRanger pipeline  including gene expression and spatial contents. For 10x Genomics single cell RNA Seq: output of CellRanger pipeline  including gene expression  features and barcodes. Supplementary files format and content: * image.tif: Tissue section used for Spatial Transcriptomics experiment.", "Zebrafish melanomas BRAF V600E", null, "For spatial transcriptomics using the Visium platform from 10X genomics: Adult tumor bearing fish were euthanized on ice and washed in 1X PBS. post dissection of the head and tail  the remaining tissue was equilibrated in cold OCT for 2 minutes  before transfer to a tissue mold filled with fresh OCT for snap freezing in liquid nitrogen chilled isopentane. Tissue blocks were stored at  80\u00b0C. For cryosectioning  both the tissue block and the ST slide were equilibrated inside the cryostat for 15 30 minutes at 16\u00b0C before sectioning. Transverse sections through the entire fish were cut at a thickness of 10 \u00b5m and immediately placed on the ST slide Visium Spatial Gene Expression Slides  10X Genomics. ST slides containing sections were stored at  80\u00b0C for a maximum of one week before use. For single cell RNA seq using the 10X genomics 3\u2019 GEX v3 platform: Adult tumor bearing fish were dissected to obtain only the tumor and surrounding tissues i.e head and tail were removed. Tissue was minced with a fresh scalpel and incubated in 0.16 mg/mL liberase Sigma Aldrich #5401020001 in 0.9X PBS for 15 minutes at RT. Tissue was then further dissociated by repeated pipetting with a wide bore P1000  followed by incubation for an additional 15 minutes at RT. post adding 500 uL FBS to stop the dissociation reaction  samples were filtered through a 70 \u00b5m filter and centrifuged at 500g for 5 minutes at RT. The resulting pellet was resuspended in DMEM supplemented with 2% FBS  and cells were sorted at room temperature to remove debris and doublets  using a BD FACSAria III cell sorter BD Biosciences. Equal numbers of GFP+ tumor and GFP  macroenvironment cells were collected.\u00a0 For spatial transcriptomics using the Visium platform from 10X genomics: Samples were processed according to the Visium Spatial Gene Expression User Guide 10X Genomics and all reagents were from the Visium Spatial Gene Expression Kit 10X Genomics. Briefly  sections were fixed in chilled methanol for 30 min at  20\u00b0C  stained with hematoxylin and eosin  and mounted in 85% glycerol for imaging. Imaging was performed on a Leica SCN400 F whole slide scanner at 40X magnification. post imaging  sections were permeabilized at 37\u00b0C for 45 minutes. post permeabilization  the on slide reverse transcription RT reaction was performed at 53\u00b0C for 2 hours. Permeabilization time and RT reaction length were determined using the Visium Spatial Tissue Optimization Kit 10X Genomics. Second strand synthesis was subsequently performed on slide for 15 minutes at 65\u00b0C. All on slide reactions were performed in a thermocycler with a metal slide adaptor plate. Following second strand synthesis  samples were transferred to tubes for cDNA amplification and cleanup. Library quality was assayed using a Bioanalyzer High Sensitivity chip Agilent. For single cell RNA seq using the 10X genomics 3\u2019 GEX v3 platform: Equal numbers of sorted GFP+ tumor and GFP  macroenvironment cells were centrifuged at 300g for 5 minutes at RT  and resuspended in DMEM + 10% FBS. Droplet based scRNA seq was performed using the Chromium Single Cell 3\u2019 Library & Gel Bead Kit v3 10X Genomics and Chromium Single Cell 3\u2019 Chip G 10X Genomics. Approximately 10 000 cells from two fish were split encapsulated in a single v3 reaction. GEM generation and library preparation were performed according to manufacturer\u2019s instructions.", null, "sample type:Tissue cryosections", "GSM4838131", "GSM4838131: Visium A; Danio rerio; RNA Seq", "GSM4838131", null, "1", "For spatial transcriptomics using the Visium platform from 10X genomics: Adult tumor bearing fish were euthanized on ice and washed in 1X PBS. post dissection of the head and tail  the remaining tissue was equilibrated in cold OCT for 2 minutes  before transfer to a tissue mold filled with fresh OCT for snap freezing in liquid nitrogen chilled isopentane. Tissue blocks were stored at  80\u00b0C. For cryosectioning  both the tissue block and the ST slide were equilibrated inside the cryostat for 15 30 minutes at 16\u00b0C before sectioning. Transverse sections through the entire fish were cut at a thickness of 10 \u00b5m and immediately placed on the ST slide Visium Spatial Gene Expression Slides  10X Genomics. ST slides containing sections were stored at  80\u00b0C for a maximum of one week before use. For single cell RNA seq using the 10X genomics three prime GEX v3 platform: Adult tumor bearing fish were dissected to obtain only the tumor and surrounding tissues i.e head and tail were removed. Tissue was minced with a fresh scalpel and incubated in 0.16 mg/mL liberase Sigma Aldrich #5401020001 in 0.9X PBS for 15 minutes at RT. Tissue was then further dissociated by repeated pipetting with a wide bore P1000  followed by incubation for an additional 15 minutes at RT. post adding 500 uL FBS to stop the dissociation reaction  samples were filtered through a 70 \u00b5m filter and centrifuged at 500g for 5 minutes at RT. The resulting pellet was resuspended in DMEM supplemented with 2% FBS  and cells were sorted at room temperature to remove debris and doublets  using a BD FACSAria III cell sorter BD Biosciences. Equal numbers of GFP+ tumor and GFP  macroenvironment cells were collected.  For spatial transcriptomics using the Visium platform from 10X genomics: Samples were processed according to the Visium Spatial Gene Expression User Guide 10X Genomics and all reagents were from the Visium Spatial Gene Expression Kit 10X Genomics. Briefly  sections were fixed in chilled methanol for 30 min at  20\u00b0C  stained with hematoxylin and eosin  and mounted in 85% glycerol for imaging. Imaging was performed on a Leica SCN400 F whole slide scanner at 40X magnification. post imaging  sections were permeabilized at 37\u00b0C for 45 minutes. post permeabilization  the on slide reverse transcription RT reaction was performed at 53\u00b0C for 2 hours. Permeabilization time and RT reaction length were determined using the Visium Spatial Tissue Optimization Kit 10X Genomics. Second strand synthesis was subsequently performed on slide for 15 minutes at 65\u00b0C. All on slide reactions were performed in a thermocycler with a metal slide adaptor plate. Following second strand synthesis  samples were transferred to tubes for cDNA amplification and cleanup. Library quality was assayed using a Bioanalyzer High Sensitivity chip Agilent. For single cell RNA seq using the 10X genomics three prime GEX v3 platform: Equal numbers of sorted GFP+ tumor and GFP  macroenvironment cells were centrifuged at 300g for 5 minutes at RT  and resuspended in DMEM + 10% FBS. Droplet based scRNA seq was performed using the Chromium Single Cell three prime Library & Gel Bead Kit v3 10X Genomics and Chromium Single Cell three prime Chip G 10X Genomics. Approximately 10 000 cells from two fish were split encapsulated in a single v3 reaction. GEM generation and library preparation were performed according to manufacturer's instructions.", "GEO Accession:GSM4838131", "RNA-Seq", "TRANSCRIPTOMIC", "cDNA", "PAIRED", "ILLUMINA", "NextSeq 500", null, "SRP287858", null, null, "Visium_Sample_A_S1_L001_R1_001.fastq.gz Visium_Sample_A_S1_L001_R2_001.fastq.gz", "fastq fastq", 8186801004.0, 55316223.0, "GSM4838131 r1", "0:28 1:120", "A:3045741900;C:1541903021;G:1757255221;T:1836190790;N:5710072", 28, 120, null, null, 3045741900, 1541903021, 1757255221, 1836190790, 5710072, "SRX9318585", "SRS7543395", "SRA1145723", "GEO", "Memorial Sloan Kettering Cancer Center", 2, 0.00549, 0.65605, 0.00319, 0.10569, 0.99734, 0.93545, 0.52914, 0.56848, 28, 120, "T", "B", "sc-like readlen", "illumina", "nextseq", "unknown", "random_priming", "unknown", "sc", "single_cell_droplet", "10x", null, "United States", "2020-10-20", "Adult", "Adult", "Cancer or Tumor", "Cancer or Tumor"], [63239, "SRR13693865", "SRX10083163", "SRS8241179", "SRP305927", "PRJNA701473", "Single cell RNA seq analysis for normal lymphocytes and IRF4 driven zebrafish tumors", "GSE166646", "Transcriptome Analysis", "Single cell RNA seq analysis was carried out for 1 normal sample from a control zebrafish line lck mCherry and 5 non tumor and 14 tumor samples from the IRF4 transgenic line lck IRF4.  Tumor cells were harvested from the animals with or without xxx p53 mutation at different time points of tumor development. Overall design: Human IRF4 gene was overexpressed together with mCherry under the zebrafish lck promoter.  Samples were harvested from control or IRF4 transgenic zebrafish lck IRF4 with or without xxx p53 mutation. mCherry positive cells sorted by flow cytometry.  Normal cells was prepared from a control zebrafish which overexpresses only mCherry.  Single cell RNA seq analysis was performed by 10X Genomics using three prime Chromium Single Cell Technique.", "parent bioproject:PRJNA701471", "pubmed:35504924", null, "Tumor cells  Late stage  IRF4;p53+/  fish 5 scRNA Seq", "GSM5076953", null, "source name:Zebrafish cells  transgenic|tissue:tumors driven by overexpression of human IRF4|sorted cells:mCherry sorted cells|genotype:IRF4 overexpression and p53 mutation|time:Late stage", "Tumor cells  Late stage  IRF4;p53+/  fish 5 scRNA Seq", "Annotations from Ensembl GRCz11 for zebrafish genes and transcripts were used and concatenated with mCherry and human IRF4 ENSG00000137265 gene information.  Single cell data were generated using mkref from cellranger package. Alignment  barcode assignation  and generation of cell gene count matrices were all performed using cellranger count from 10x genomics version 3.1.0 cellranger count   id zv11 {sampleID}   fastqs={directory scSeq}   sample={sampleID}  transcriptome={mkgtf generated STAR library} Genome build: GRCz11 Danio Rerio + mCherry + Human IRF4 ENSG00000137265 Supplementary files format and content: HDF5 Gene Barcode Matrix format containing UMI counts of each gene for individual cells.  The data files can be deconvoluted to tsv and mtx files using cellranger reanalyze", "Zebrafish cells  transgenic", "No treatment", "post sorting  the cells were washed and processed for barcoding using the 10x Genomics Chromium Single Cell three prime Solution v2 kit following manufacturer's instructions. Illumina P5 and P7 sequences and sample index sequences are added during the Sample Index PCR. The final library fragments contain the P5  P7  Read 1 and Read 2 sequences used in Illumina bridge amplification and sequencing. Additionally  each fragment contains the 10x Barcode  UMI and cDNA insert sequence used in data analysis. Single cell RNA Seq", "The human IRF4 gene and mCherry fluorescent marker gene were transduced under the zebrafish lck promoter in zebrafish.  post the development of lymphoma phenotype  tumor cells were harvested and sorted by flow cytometry based on mCherry fluorescence expression.  A zebrafish which was transduced only with mCherry was used as a control.", "tissue:tumors driven by overexpression of human IRF4|sorted cells:mCherry sorted cells|genotype:IRF4 overexpression and p53 mutation|time:Late stage", "GSM5076953", "GSM5076953: Tumor cells  Late stage  IRF4;p53+/  fish 5 scRNA Seq; Danio rerio; RNA Seq", "GSM5076953", null, "1", "post sorting  the cells were washed and processed for barcoding using the 10x Genomics Chromium Single Cell three prime Solution v2 kit following manufacturer's instructions. Illumina P5 and P7 sequences and sample index sequences are added during the Sample Index PCR. The final library fragments contain the P5  P7  Read 1 and Read 2 sequences used in Illumina bridge amplification and sequencing. Additionally  each fragment contains the 10x Barcode  UMI and cDNA insert sequence used in data analysis. Single cell RNA Seq", "GEO Accession:GSM5076953", "RNA-Seq", "TRANSCRIPTOMIC", "cDNA", "PAIRED", "ILLUMINA", "HiSeq X Ten", null, "SRP305927", null, "loader:fastq load.py|options:  platform=Illumina   readTypes=TTB   read1PairFiles=S3 I1.fastq.gz   read2PairFiles=S3 R1.fastq.gz   read3PairFiles=S3 R2.fastq.gz", null, null, 30902398692.0, 234109081.0, "GSM5076953 r1", "0:8 1:26 2:98", "A:8591012397;C:7005723022;G:7425233397;T:7870465271;N:9964605", 8, 26, 98, null, 8591012397, 7005723022, 7425233397, 7870465271, 9964605, "SRX10083163", "SRS8241179", "SRA1195246", "GEO", "Takaomi Sanda Lab, Cancer Science Institute, National University of Singapore", 1, 0.92664, null, 0.18689, null, 0.83376, null, 0.51575, null, 98, null, "B", null, "usable mapping rate", "illumina", "hiseq_era", "unknown", "cdna_unspecified", "unknown", "sc", "single_cell_droplet", "10x", null, "Singapore", "2021-02-11", "Undetermined", "Undetermined", "Cancer or Tumor", "Cancer or Tumor"], [63240, "SRR13693864", "SRX10083162", "SRS8241178", "SRP305927", "PRJNA701473", "Single cell RNA seq analysis for normal lymphocytes and IRF4 driven zebrafish tumors", "GSE166646", "Transcriptome Analysis", "Single cell RNA seq analysis was carried out for 1 normal sample from a control zebrafish line lck mCherry and 5 non tumor and 14 tumor samples from the IRF4 transgenic line lck IRF4.  Tumor cells were harvested from the animals with or without xxx p53 mutation at different time points of tumor development. Overall design: Human IRF4 gene was overexpressed together with mCherry under the zebrafish lck promoter.  Samples were harvested from control or IRF4 transgenic zebrafish lck IRF4 with or without xxx p53 mutation. mCherry positive cells sorted by flow cytometry.  Normal cells was prepared from a control zebrafish which overexpresses only mCherry.  Single cell RNA seq analysis was performed by 10X Genomics using three prime Chromium Single Cell Technique.", "parent bioproject:PRJNA701471", "pubmed:35504924", null, "Tumor cells  Late stage  IRF4;p53+/  fish 4 scRNA Seq", "GSM5076952", null, "source name:Zebrafish cells  transgenic|tissue:tumors driven by overexpression of human IRF4|sorted cells:mCherry sorted cells|genotype:IRF4 overexpression and p53 mutation|time:Late stage", "Tumor cells  Late stage  IRF4;p53+/  fish 4 scRNA Seq", "Annotations from Ensembl GRCz11 for zebrafish genes and transcripts were used and concatenated with mCherry and human IRF4 ENSG00000137265 gene information.  Single cell data were generated using mkref from cellranger package. Alignment  barcode assignation  and generation of cell gene count matrices were all performed using cellranger count from 10x genomics version 3.1.0 cellranger count   id zv11 {sampleID}   fastqs={directory scSeq}   sample={sampleID}  transcriptome={mkgtf generated STAR library} Genome build: GRCz11 Danio Rerio + mCherry + Human IRF4 ENSG00000137265 Supplementary files format and content: HDF5 Gene Barcode Matrix format containing UMI counts of each gene for individual cells.  The data files can be deconvoluted to tsv and mtx files using cellranger reanalyze", "Zebrafish cells  transgenic", "No treatment", "post sorting  the cells were washed and processed for barcoding using the 10x Genomics Chromium Single Cell three prime Solution v2 kit following manufacturer's instructions. Illumina P5 and P7 sequences and sample index sequences are added during the Sample Index PCR. The final library fragments contain the P5  P7  Read 1 and Read 2 sequences used in Illumina bridge amplification and sequencing. Additionally  each fragment contains the 10x Barcode  UMI and cDNA insert sequence used in data analysis. Single cell RNA Seq", "The human IRF4 gene and mCherry fluorescent marker gene were transduced under the zebrafish lck promoter in zebrafish.  post the development of lymphoma phenotype  tumor cells were harvested and sorted by flow cytometry based on mCherry fluorescence expression.  A zebrafish which was transduced only with mCherry was used as a control.", "tissue:tumors driven by overexpression of human IRF4|sorted cells:mCherry sorted cells|genotype:IRF4 overexpression and p53 mutation|time:Late stage", "GSM5076952", "GSM5076952: Tumor cells  Late stage  IRF4;p53+/  fish 4 scRNA Seq; Danio rerio; RNA Seq", "GSM5076952", null, "1", "post sorting  the cells were washed and processed for barcoding using the 10x Genomics Chromium Single Cell three prime Solution v2 kit following manufacturer's instructions. Illumina P5 and P7 sequences and sample index sequences are added during the Sample Index PCR. The final library fragments contain the P5  P7  Read 1 and Read 2 sequences used in Illumina bridge amplification and sequencing. Additionally  each fragment contains the 10x Barcode  UMI and cDNA insert sequence used in data analysis. Single cell RNA Seq", "GEO Accession:GSM5076952", "RNA-Seq", "TRANSCRIPTOMIC", "cDNA", "PAIRED", "ILLUMINA", "HiSeq X Ten", null, "SRP305927", null, "loader:fastq load.py|options:  platform=Illumina   readTypes=TTB   read1PairFiles=S2 I1.fastq.gz   read2PairFiles=S2 R1.fastq.gz   read3PairFiles=S2 R2.fastq.gz", "S2_I1.fastq S2_R1.fastq S2_R2.fastq", "fastq fastq fastq", 31435037700.0, 238144225.0, "GSM5076952 r1", "0:8 1:26 2:98", "A:8766861031;C:6971129836;G:7458655794;T:8228099570;N:10291469", 8, 26, 98, null, 8766861031, 6971129836, 7458655794, 8228099570, 10291469, "SRX10083162", "SRS8241178", "SRA1195246", "GEO", "Takaomi Sanda Lab, Cancer Science Institute, National University of Singapore", 1, 0.92786, null, 0.2437, null, 0.82406, null, 0.51326, null, 98, null, "B", null, "usable mapping rate", "illumina", "hiseq_era", "unknown", "cdna_unspecified", "unknown", "sc", "single_cell_droplet", "10x", null, "Singapore", "2021-02-11", "Undetermined", "Undetermined", "Cancer or Tumor", "Cancer or Tumor"], [63241, "SRR13693863", "SRX10083161", "SRS8241177", "SRP305927", "PRJNA701473", "Single cell RNA seq analysis for normal lymphocytes and IRF4 driven zebrafish tumors", "GSE166646", "Transcriptome Analysis", "Single cell RNA seq analysis was carried out for 1 normal sample from a control zebrafish line lck mCherry and 5 non tumor and 14 tumor samples from the IRF4 transgenic line lck IRF4.  Tumor cells were harvested from the animals with or without xxx p53 mutation at different time points of tumor development. Overall design: Human IRF4 gene was overexpressed together with mCherry under the zebrafish lck promoter.  Samples were harvested from control or IRF4 transgenic zebrafish lck IRF4 with or without xxx p53 mutation. mCherry positive cells sorted by flow cytometry.  Normal cells was prepared from a control zebrafish which overexpresses only mCherry.  Single cell RNA seq analysis was performed by 10X Genomics using three prime Chromium Single Cell Technique.", "parent bioproject:PRJNA701471", "pubmed:35504924", null, "Tumor cells  Late stage  IRF4;p53+/  fish 3 scRNA Seq", "GSM5076951", null, "source name:Zebrafish cells  transgenic|tissue:tumors driven by overexpression of human IRF4|sorted cells:mCherry sorted cells|genotype:IRF4 overexpression and p53 mutation|time:Late stage", "Tumor cells  Late stage  IRF4;p53+/  fish 3 scRNA Seq", "Annotations from Ensembl GRCz11 for zebrafish genes and transcripts were used and concatenated with mCherry and human IRF4 ENSG00000137265 gene information.  Single cell data were generated using mkref from cellranger package. Alignment  barcode assignation  and generation of cell gene count matrices were all performed using cellranger count from 10x genomics version 3.1.0 cellranger count   id zv11 {sampleID}   fastqs={directory scSeq}   sample={sampleID}  transcriptome={mkgtf generated STAR library} Genome build: GRCz11 Danio Rerio + mCherry + Human IRF4 ENSG00000137265 Supplementary files format and content: HDF5 Gene Barcode Matrix format containing UMI counts of each gene for individual cells.  The data files can be deconvoluted to tsv and mtx files using cellranger reanalyze", "Zebrafish cells  transgenic", "No treatment", "post sorting  the cells were washed and processed for barcoding using the 10x Genomics Chromium Single Cell three prime Solution v2 kit following manufacturer's instructions. Illumina P5 and P7 sequences and sample index sequences are added during the Sample Index PCR. The final library fragments contain the P5  P7  Read 1 and Read 2 sequences used in Illumina bridge amplification and sequencing. Additionally  each fragment contains the 10x Barcode  UMI and cDNA insert sequence used in data analysis. Single cell RNA Seq", "The human IRF4 gene and mCherry fluorescent marker gene were transduced under the zebrafish lck promoter in zebrafish.  post the development of lymphoma phenotype  tumor cells were harvested and sorted by flow cytometry based on mCherry fluorescence expression.  A zebrafish which was transduced only with mCherry was used as a control.", "tissue:tumors driven by overexpression of human IRF4|sorted cells:mCherry sorted cells|genotype:IRF4 overexpression and p53 mutation|time:Late stage", "GSM5076951", "GSM5076951: Tumor cells  Late stage  IRF4;p53+/  fish 3 scRNA Seq; Danio rerio; RNA Seq", "GSM5076951", null, "1", "post sorting  the cells were washed and processed for barcoding using the 10x Genomics Chromium Single Cell three prime Solution v2 kit following manufacturer's instructions. Illumina P5 and P7 sequences and sample index sequences are added during the Sample Index PCR. The final library fragments contain the P5  P7  Read 1 and Read 2 sequences used in Illumina bridge amplification and sequencing. Additionally  each fragment contains the 10x Barcode  UMI and cDNA insert sequence used in data analysis. Single cell RNA Seq", "GEO Accession:GSM5076951", "RNA-Seq", "TRANSCRIPTOMIC", "cDNA", "PAIRED", "ILLUMINA", "HiSeq X Ten", null, "SRP305927", null, "loader:fastq load.py|options:  platform=Illumina   readTypes=TTB   read1PairFiles=D3 I1.fastq.gz   read2PairFiles=D3 R1.fastq.gz   read3PairFiles=D3 R2.fastq.gz", "D3_I1.fastq.gz D3_R1.fastq.gz D3_R2.fastq.gz", "fastq fastq fastq", 28995027468.0, 219659299.0, "GSM5076951 r1", "0:8 1:26 2:98", "A:8296536133;C:6414043957;G:6689913049;T:7585241915;N:9292414", 8, 26, 98, null, 8296536133, 6414043957, 6689913049, 7585241915, 9292414, "SRX10083161", "SRS8241177", "SRA1195246", "GEO", "Takaomi Sanda Lab, Cancer Science Institute, National University of Singapore", 1, 0.91752, null, 0.20118, null, 0.82903, null, 0.51629, null, 98, null, "B", null, "usable mapping rate", "illumina", "hiseq_era", "unknown", "cdna_unspecified", "unknown", "sc", "single_cell_droplet", "10x", null, "Singapore", "2021-02-11", "Undetermined", "Undetermined", "Cancer or Tumor", "Cancer or Tumor"], [63242, "SRR13693862", "SRX10083160", "SRS8241176", "SRP305927", "PRJNA701473", "Single cell RNA seq analysis for normal lymphocytes and IRF4 driven zebrafish tumors", "GSE166646", "Transcriptome Analysis", "Single cell RNA seq analysis was carried out for 1 normal sample from a control zebrafish line lck mCherry and 5 non tumor and 14 tumor samples from the IRF4 transgenic line lck IRF4.  Tumor cells were harvested from the animals with or without xxx p53 mutation at different time points of tumor development. Overall design: Human IRF4 gene was overexpressed together with mCherry under the zebrafish lck promoter.  Samples were harvested from control or IRF4 transgenic zebrafish lck IRF4 with or without xxx p53 mutation. mCherry positive cells sorted by flow cytometry.  Normal cells was prepared from a control zebrafish which overexpresses only mCherry.  Single cell RNA seq analysis was performed by 10X Genomics using three prime Chromium Single Cell Technique.", "parent bioproject:PRJNA701471", "pubmed:35504924", null, "Tumor cells  Late stage  IRF4;p53+/  fish 2 scRNA Seq", "GSM5076950", null, "source name:Zebrafish cells  transgenic|tissue:tumors driven by overexpression of human IRF4|sorted cells:mCherry sorted cells|genotype:IRF4 overexpression and p53 mutation|time:Late stage", "Tumor cells  Late stage  IRF4;p53+/  fish 2 scRNA Seq", "Annotations from Ensembl GRCz11 for zebrafish genes and transcripts were used and concatenated with mCherry and human IRF4 ENSG00000137265 gene information.  Single cell data were generated using mkref from cellranger package. Alignment  barcode assignation  and generation of cell gene count matrices were all performed using cellranger count from 10x genomics version 3.1.0 cellranger count   id zv11 {sampleID}   fastqs={directory scSeq}   sample={sampleID}  transcriptome={mkgtf generated STAR library} Genome build: GRCz11 Danio Rerio + mCherry + Human IRF4 ENSG00000137265 Supplementary files format and content: HDF5 Gene Barcode Matrix format containing UMI counts of each gene for individual cells.  The data files can be deconvoluted to tsv and mtx files using cellranger reanalyze", "Zebrafish cells  transgenic", "No treatment", "post sorting  the cells were washed and processed for barcoding using the 10x Genomics Chromium Single Cell three prime Solution v2 kit following manufacturer's instructions. Illumina P5 and P7 sequences and sample index sequences are added during the Sample Index PCR. The final library fragments contain the P5  P7  Read 1 and Read 2 sequences used in Illumina bridge amplification and sequencing. Additionally  each fragment contains the 10x Barcode  UMI and cDNA insert sequence used in data analysis. Single cell RNA Seq", "The human IRF4 gene and mCherry fluorescent marker gene were transduced under the zebrafish lck promoter in zebrafish.  post the development of lymphoma phenotype  tumor cells were harvested and sorted by flow cytometry based on mCherry fluorescence expression.  A zebrafish which was transduced only with mCherry was used as a control.", "tissue:tumors driven by overexpression of human IRF4|sorted cells:mCherry sorted cells|genotype:IRF4 overexpression and p53 mutation|time:Late stage", "GSM5076950", "GSM5076950: Tumor cells  Late stage  IRF4;p53+/  fish 2 scRNA Seq; Danio rerio; RNA Seq", "GSM5076950", null, "1", "post sorting  the cells were washed and processed for barcoding using the 10x Genomics Chromium Single Cell three prime Solution v2 kit following manufacturer's instructions. Illumina P5 and P7 sequences and sample index sequences are added during the Sample Index PCR. The final library fragments contain the P5  P7  Read 1 and Read 2 sequences used in Illumina bridge amplification and sequencing. Additionally  each fragment contains the 10x Barcode  UMI and cDNA insert sequence used in data analysis. Single cell RNA Seq", "GEO Accession:GSM5076950", "RNA-Seq", "TRANSCRIPTOMIC", "cDNA", "PAIRED", "ILLUMINA", "HiSeq X Ten", null, "SRP305927", null, "loader:fastq load.py|options:  platform=Illumina   readTypes=TTB   read1PairFiles=D2 I1.fastq.gz   read2PairFiles=D2 R1.fastq.gz   read3PairFiles=D2 R2.fastq.gz", "D2_I1.fastq.gz D2_R1.fastq.gz D2_R2.fastq.gz", "fastq fastq fastq", 34413827844.0, 260710817.0, "GSM5076950 r1", "0:8 1:26 2:98", "A:9806323881;C:7657614846;G:7929340289;T:9009399182;N:11149646", 8, 26, 98, null, 9806323881, 7657614846, 7929340289, 9009399182, 11149646, "SRX10083160", "SRS8241176", "SRA1195246", "GEO", "Takaomi Sanda Lab, Cancer Science Institute, National University of Singapore", 1, 0.91903, null, 0.19966, null, 0.83591, null, 0.53703, null, 98, null, "B", null, "usable mapping rate", "illumina", "hiseq_era", "unknown", "cdna_unspecified", "unknown", "sc", "single_cell_droplet", "10x", null, "Singapore", "2021-02-11", "Undetermined", "Undetermined", "Cancer or Tumor", "Cancer or Tumor"], [63243, "SRR13693861", "SRX10083159", "SRS8241175", "SRP305927", "PRJNA701473", "Single cell RNA seq analysis for normal lymphocytes and IRF4 driven zebrafish tumors", "GSE166646", "Transcriptome Analysis", "Single cell RNA seq analysis was carried out for 1 normal sample from a control zebrafish line lck mCherry and 5 non tumor and 14 tumor samples from the IRF4 transgenic line lck IRF4.  Tumor cells were harvested from the animals with or without xxx p53 mutation at different time points of tumor development. Overall design: Human IRF4 gene was overexpressed together with mCherry under the zebrafish lck promoter.  Samples were harvested from control or IRF4 transgenic zebrafish lck IRF4 with or without xxx p53 mutation. mCherry positive cells sorted by flow cytometry.  Normal cells was prepared from a control zebrafish which overexpresses only mCherry.  Single cell RNA seq analysis was performed by 10X Genomics using three prime Chromium Single Cell Technique.", "parent bioproject:PRJNA701471", "pubmed:35504924", null, "Tumor cells  Late stage  IRF4;p53+/  fish 1 scRNA Seq", "GSM5076949", null, "source name:Zebrafish cells  transgenic|tissue:tumors driven by overexpression of human IRF4|sorted cells:mCherry sorted cells|genotype:IRF4 overexpression and p53 mutation|time:Late stage", "Tumor cells  Late stage  IRF4;p53+/  fish 1 scRNA Seq", "Annotations from Ensembl GRCz11 for zebrafish genes and transcripts were used and concatenated with mCherry and human IRF4 ENSG00000137265 gene information.  Single cell data were generated using mkref from cellranger package. Alignment  barcode assignation  and generation of cell gene count matrices were all performed using cellranger count from 10x genomics version 3.1.0 cellranger count   id zv11 {sampleID}   fastqs={directory scSeq}   sample={sampleID}  transcriptome={mkgtf generated STAR library} Genome build: GRCz11 Danio Rerio + mCherry + Human IRF4 ENSG00000137265 Supplementary files format and content: HDF5 Gene Barcode Matrix format containing UMI counts of each gene for individual cells.  The data files can be deconvoluted to tsv and mtx files using cellranger reanalyze", "Zebrafish cells  transgenic", "No treatment", "post sorting  the cells were washed and processed for barcoding using the 10x Genomics Chromium Single Cell three prime Solution v2 kit following manufacturer's instructions. Illumina P5 and P7 sequences and sample index sequences are added during the Sample Index PCR. The final library fragments contain the P5  P7  Read 1 and Read 2 sequences used in Illumina bridge amplification and sequencing. Additionally  each fragment contains the 10x Barcode  UMI and cDNA insert sequence used in data analysis. Single cell RNA Seq", "The human IRF4 gene and mCherry fluorescent marker gene were transduced under the zebrafish lck promoter in zebrafish.  post the development of lymphoma phenotype  tumor cells were harvested and sorted by flow cytometry based on mCherry fluorescence expression.  A zebrafish which was transduced only with mCherry was used as a control.", "tissue:tumors driven by overexpression of human IRF4|sorted cells:mCherry sorted cells|genotype:IRF4 overexpression and p53 mutation|time:Late stage", "GSM5076949", "GSM5076949: Tumor cells  Late stage  IRF4;p53+/  fish 1 scRNA Seq; Danio rerio; RNA Seq", "GSM5076949", null, "1", "post sorting  the cells were washed and processed for barcoding using the 10x Genomics Chromium Single Cell three prime Solution v2 kit following manufacturer's instructions. Illumina P5 and P7 sequences and sample index sequences are added during the Sample Index PCR. The final library fragments contain the P5  P7  Read 1 and Read 2 sequences used in Illumina bridge amplification and sequencing. Additionally  each fragment contains the 10x Barcode  UMI and cDNA insert sequence used in data analysis. Single cell RNA Seq", "GEO Accession:GSM5076949", "RNA-Seq", "TRANSCRIPTOMIC", "cDNA", "PAIRED", "ILLUMINA", "HiSeq X Ten", null, "SRP305927", null, "loader:fastq load.py|options:  platform=Illumina   readTypes=TTB   read1PairFiles=D1 I1.fastq.gz   read2PairFiles=D1 R1.fastq.gz   read3PairFiles=D1 R2.fastq.gz", "D1_I1.fastq.gz D1_R1.fastq.gz D1_R2.fastq.gz", "fastq fastq fastq", 32611994976.0, 247060568.0, "GSM5076949 r1", "0:8 1:26 2:98", "A:9284005966;C:7280091614;G:7543060588;T:8494420994;N:10415814", 8, 26, 98, null, 9284005966, 7280091614, 7543060588, 8494420994, 10415814, "SRX10083159", "SRS8241175", "SRA1195246", "GEO", "Takaomi Sanda Lab, Cancer Science Institute, National University of Singapore", 1, 0.92638, null, 0.18797, null, 0.83713, null, 0.55228, null, 98, null, "B", null, "usable mapping rate", "illumina", "hiseq_era", "unknown", "cdna_unspecified", "unknown", "sc", "single_cell_droplet", "10x", null, "Singapore", "2021-02-11", "Undetermined", "Undetermined", "Cancer or Tumor", "Cancer or Tumor"], [63244, "SRR13693860", "SRX10083158", "SRS8241174", "SRP305927", "PRJNA701473", "Single cell RNA seq analysis for normal lymphocytes and IRF4 driven zebrafish tumors", "GSE166646", "Transcriptome Analysis", "Single cell RNA seq analysis was carried out for 1 normal sample from a control zebrafish line lck mCherry and 5 non tumor and 14 tumor samples from the IRF4 transgenic line lck IRF4.  Tumor cells were harvested from the animals with or without xxx p53 mutation at different time points of tumor development. Overall design: Human IRF4 gene was overexpressed together with mCherry under the zebrafish lck promoter.  Samples were harvested from control or IRF4 transgenic zebrafish lck IRF4 with or without xxx p53 mutation. mCherry positive cells sorted by flow cytometry.  Normal cells was prepared from a control zebrafish which overexpresses only mCherry.  Single cell RNA seq analysis was performed by 10X Genomics using three prime Chromium Single Cell Technique.", "parent bioproject:PRJNA701471", "pubmed:35504924", null, "Tumor cells  Late stage  Ick:IRF4 fish 6 scRNA Seq", "GSM5076948", null, "source name:Zebrafish cells  transgenic|tissue:tumors driven by overexpression of human IRF4|sorted cells:mCherry sorted cells|genotype:IRF4 overexpression|time:Late stage", "Tumor cells  Late stage  Ick:IRF4 fish 6 scRNA Seq", "Annotations from Ensembl GRCz11 for zebrafish genes and transcripts were used and concatenated with mCherry and human IRF4 ENSG00000137265 gene information.  Single cell data were generated using mkref from cellranger package. Alignment  barcode assignation  and generation of cell gene count matrices were all performed using cellranger count from 10x genomics version 3.1.0 cellranger count   id zv11 {sampleID}   fastqs={directory scSeq}   sample={sampleID}  transcriptome={mkgtf generated STAR library} Genome build: GRCz11 Danio Rerio + mCherry + Human IRF4 ENSG00000137265 Supplementary files format and content: HDF5 Gene Barcode Matrix format containing UMI counts of each gene for individual cells.  The data files can be deconvoluted to tsv and mtx files using cellranger reanalyze", "Zebrafish cells  transgenic", "No treatment", "post sorting  the cells were washed and processed for barcoding using the 10x Genomics Chromium Single Cell three prime Solution v2 kit following manufacturer's instructions. Illumina P5 and P7 sequences and sample index sequences are added during the Sample Index PCR. The final library fragments contain the P5  P7  Read 1 and Read 2 sequences used in Illumina bridge amplification and sequencing. Additionally  each fragment contains the 10x Barcode  UMI and cDNA insert sequence used in data analysis. Single cell RNA Seq", "The human IRF4 gene and mCherry fluorescent marker gene were transduced under the zebrafish lck promoter in zebrafish.  post the development of lymphoma phenotype  tumor cells were harvested and sorted by flow cytometry based on mCherry fluorescence expression.  A zebrafish which was transduced only with mCherry was used as a control.", "tissue:tumors driven by overexpression of human IRF4|sorted cells:mCherry sorted cells|genotype:IRF4 overexpression|time:Late stage", "GSM5076948", "GSM5076948: Tumor cells  Late stage  Ick:IRF4 fish 6 scRNA Seq; Danio rerio; RNA Seq", "GSM5076948", null, "1", "post sorting  the cells were washed and processed for barcoding using the 10x Genomics Chromium Single Cell three prime Solution v2 kit following manufacturer's instructions. Illumina P5 and P7 sequences and sample index sequences are added during the Sample Index PCR. The final library fragments contain the P5  P7  Read 1 and Read 2 sequences used in Illumina bridge amplification and sequencing. Additionally  each fragment contains the 10x Barcode  UMI and cDNA insert sequence used in data analysis. Single cell RNA Seq", "GEO Accession:GSM5076948", "RNA-Seq", "TRANSCRIPTOMIC", "cDNA", "PAIRED", "ILLUMINA", "HiSeq X Ten", null, "SRP305927", null, "loader:fastq load.py|options:  platform=Illumina   readTypes=TTB   read1PairFiles=3S I1.fastq.gz   read2PairFiles=3S R1.fastq.gz   read3PairFiles=3S R2.fastq.gz", "3S_I1.fastq.gz 3S_R1.fastq.gz 3S_R2.fastq.gz", "fastq fastq fastq", 27615581268.0, 209208949.0, "GSM5076948 r1", "0:8 1:26 2:98", "A:7903060121;C:6181635403;G:6459419292;T:7062664494;N:8801958", 8, 26, 98, null, 7903060121, 6181635403, 6459419292, 7062664494, 8801958, "SRX10083158", "SRS8241174", "SRA1195246", "GEO", "Takaomi Sanda Lab, Cancer Science Institute, National University of Singapore", 1, 0.91885, null, 0.167, null, 0.84952, null, 0.49561, null, 98, null, "B", null, "usable mapping rate", "illumina", "hiseq_era", "unknown", "cdna_unspecified", "unknown", "sc", "single_cell_droplet", "10x", null, "Singapore", "2021-02-11", "Undetermined", "Undetermined", "Cancer or Tumor", "Cancer or Tumor"], [63245, "SRR13693859", "SRX10083157", "SRS8241173", "SRP305927", "PRJNA701473", "Single cell RNA seq analysis for normal lymphocytes and IRF4 driven zebrafish tumors", "GSE166646", "Transcriptome Analysis", "Single cell RNA seq analysis was carried out for 1 normal sample from a control zebrafish line lck mCherry and 5 non tumor and 14 tumor samples from the IRF4 transgenic line lck IRF4.  Tumor cells were harvested from the animals with or without xxx p53 mutation at different time points of tumor development. Overall design: Human IRF4 gene was overexpressed together with mCherry under the zebrafish lck promoter.  Samples were harvested from control or IRF4 transgenic zebrafish lck IRF4 with or without xxx p53 mutation. mCherry positive cells sorted by flow cytometry.  Normal cells was prepared from a control zebrafish which overexpresses only mCherry.  Single cell RNA seq analysis was performed by 10X Genomics using three prime Chromium Single Cell Technique.", "parent bioproject:PRJNA701471", "pubmed:35504924", null, "Tumor cells  Late stage  Ick:IRF4 fish 5 scRNA Seq", "GSM5076947", null, "source name:Zebrafish cells  transgenic|tissue:tumors driven by overexpression of human IRF4|sorted cells:mCherry sorted cells|genotype:IRF4 overexpression|time:Late stage", "Tumor cells  Late stage  Ick:IRF4 fish 5 scRNA Seq", "Annotations from Ensembl GRCz11 for zebrafish genes and transcripts were used and concatenated with mCherry and human IRF4 ENSG00000137265 gene information.  Single cell data were generated using mkref from cellranger package. Alignment  barcode assignation  and generation of cell gene count matrices were all performed using cellranger count from 10x genomics version 3.1.0 cellranger count   id zv11 {sampleID}   fastqs={directory scSeq}   sample={sampleID}  transcriptome={mkgtf generated STAR library} Genome build: GRCz11 Danio Rerio + mCherry + Human IRF4 ENSG00000137265 Supplementary files format and content: HDF5 Gene Barcode Matrix format containing UMI counts of each gene for individual cells.  The data files can be deconvoluted to tsv and mtx files using cellranger reanalyze", "Zebrafish cells  transgenic", "No treatment", "post sorting  the cells were washed and processed for barcoding using the 10x Genomics Chromium Single Cell three prime Solution v2 kit following manufacturer's instructions. Illumina P5 and P7 sequences and sample index sequences are added during the Sample Index PCR. The final library fragments contain the P5  P7  Read 1 and Read 2 sequences used in Illumina bridge amplification and sequencing. Additionally  each fragment contains the 10x Barcode  UMI and cDNA insert sequence used in data analysis. Single cell RNA Seq", "The human IRF4 gene and mCherry fluorescent marker gene were transduced under the zebrafish lck promoter in zebrafish.  post the development of lymphoma phenotype  tumor cells were harvested and sorted by flow cytometry based on mCherry fluorescence expression.  A zebrafish which was transduced only with mCherry was used as a control.", "tissue:tumors driven by overexpression of human IRF4|sorted cells:mCherry sorted cells|genotype:IRF4 overexpression|time:Late stage", "GSM5076947", "GSM5076947: Tumor cells  Late stage  Ick:IRF4 fish 5 scRNA Seq; Danio rerio; RNA Seq", "GSM5076947", null, "1", "post sorting  the cells were washed and processed for barcoding using the 10x Genomics Chromium Single Cell three prime Solution v2 kit following manufacturer's instructions. Illumina P5 and P7 sequences and sample index sequences are added during the Sample Index PCR. The final library fragments contain the P5  P7  Read 1 and Read 2 sequences used in Illumina bridge amplification and sequencing. Additionally  each fragment contains the 10x Barcode  UMI and cDNA insert sequence used in data analysis. Single cell RNA Seq", "GEO Accession:GSM5076947", "RNA-Seq", "TRANSCRIPTOMIC", "cDNA", "PAIRED", "ILLUMINA", "HiSeq X Ten", null, "SRP305927", null, "loader:fastq load.py|options:  platform=Illumina   readTypes=TTB   read1PairFiles=2S I1.fastq.gz   read2PairFiles=2S R1.fastq.gz   read3PairFiles=2S R2.fastq.gz", "2S_I1.fastq.gz 2S_R1.fastq.gz 2S_R2.fastq.gz", "fastq fastq fastq", 27096206280.0, 205274290.0, "GSM5076947 r1", "0:8 1:26 2:98", "A:7673974628;C:6078379871;G:6323826541;T:7011380350;N:8644890", 8, 26, 98, null, 7673974628, 6078379871, 6323826541, 7011380350, 8644890, "SRX10083157", "SRS8241173", "SRA1195246", "GEO", "Takaomi Sanda Lab, Cancer Science Institute, National University of Singapore", 1, 0.92045, null, 0.17808, null, 0.83942, null, 0.50762, null, 98, null, "B", null, "usable mapping rate", "illumina", "hiseq_era", "unknown", "cdna_unspecified", "unknown", "sc", "single_cell_droplet", "10x", null, "Singapore", "2021-02-11", "Undetermined", "Undetermined", "Cancer or Tumor", "Cancer or Tumor"], [63246, "SRR13693858", "SRX10083156", "SRS8241172", "SRP305927", "PRJNA701473", "Single cell RNA seq analysis for normal lymphocytes and IRF4 driven zebrafish tumors", "GSE166646", "Transcriptome Analysis", "Single cell RNA seq analysis was carried out for 1 normal sample from a control zebrafish line lck mCherry and 5 non tumor and 14 tumor samples from the IRF4 transgenic line lck IRF4.  Tumor cells were harvested from the animals with or without xxx p53 mutation at different time points of tumor development. Overall design: Human IRF4 gene was overexpressed together with mCherry under the zebrafish lck promoter.  Samples were harvested from control or IRF4 transgenic zebrafish lck IRF4 with or without xxx p53 mutation. mCherry positive cells sorted by flow cytometry.  Normal cells was prepared from a control zebrafish which overexpresses only mCherry.  Single cell RNA seq analysis was performed by 10X Genomics using three prime Chromium Single Cell Technique.", "parent bioproject:PRJNA701471", "pubmed:35504924", null, "Tumor cells  Late stage  Ick:IRF4 fish 4 scRNA Seq", "GSM5076946", null, "source name:Zebrafish cells  transgenic|tissue:tumors driven by overexpression of human IRF4|sorted cells:mCherry sorted cells|genotype:IRF4 overexpression|time:Late stage", "Tumor cells  Late stage  Ick:IRF4 fish 4 scRNA Seq", "Annotations from Ensembl GRCz11 for zebrafish genes and transcripts were used and concatenated with mCherry and human IRF4 ENSG00000137265 gene information.  Single cell data were generated using mkref from cellranger package. Alignment  barcode assignation  and generation of cell gene count matrices were all performed using cellranger count from 10x genomics version 3.1.0 cellranger count   id zv11 {sampleID}   fastqs={directory scSeq}   sample={sampleID}  transcriptome={mkgtf generated STAR library} Genome build: GRCz11 Danio Rerio + mCherry + Human IRF4 ENSG00000137265 Supplementary files format and content: HDF5 Gene Barcode Matrix format containing UMI counts of each gene for individual cells.  The data files can be deconvoluted to tsv and mtx files using cellranger reanalyze", "Zebrafish cells  transgenic", "No treatment", "post sorting  the cells were washed and processed for barcoding using the 10x Genomics Chromium Single Cell three prime Solution v2 kit following manufacturer's instructions. Illumina P5 and P7 sequences and sample index sequences are added during the Sample Index PCR. The final library fragments contain the P5  P7  Read 1 and Read 2 sequences used in Illumina bridge amplification and sequencing. Additionally  each fragment contains the 10x Barcode  UMI and cDNA insert sequence used in data analysis. Single cell RNA Seq", "The human IRF4 gene and mCherry fluorescent marker gene were transduced under the zebrafish lck promoter in zebrafish.  post the development of lymphoma phenotype  tumor cells were harvested and sorted by flow cytometry based on mCherry fluorescence expression.  A zebrafish which was transduced only with mCherry was used as a control.", "tissue:tumors driven by overexpression of human IRF4|sorted cells:mCherry sorted cells|genotype:IRF4 overexpression|time:Late stage", "GSM5076946", "GSM5076946: Tumor cells  Late stage  Ick:IRF4 fish 4 scRNA Seq; Danio rerio; RNA Seq", "GSM5076946", null, "1", "post sorting  the cells were washed and processed for barcoding using the 10x Genomics Chromium Single Cell three prime Solution v2 kit following manufacturer's instructions. Illumina P5 and P7 sequences and sample index sequences are added during the Sample Index PCR. The final library fragments contain the P5  P7  Read 1 and Read 2 sequences used in Illumina bridge amplification and sequencing. Additionally  each fragment contains the 10x Barcode  UMI and cDNA insert sequence used in data analysis. Single cell RNA Seq", "GEO Accession:GSM5076946", "RNA-Seq", "TRANSCRIPTOMIC", "cDNA", "PAIRED", "ILLUMINA", "HiSeq X Ten", null, "SRP305927", null, "loader:fastq load.py|options:  platform=Illumina   readTypes=TTB   read1PairFiles=1S I1.fastq.gz   read2PairFiles=1S R1.fastq.gz   read3PairFiles=1S R2.fastq.gz", "1S_I1.fastq.gz 1S_R1.fastq.gz 1S_R2.fastq.gz", "fastq fastq fastq", 25321669296.0, 191830828.0, "GSM5076946 r1", "0:8 1:26 2:98", "A:7267370389;C:5631756169;G:5928757429;T:6485676974;N:8108335", 8, 26, 98, null, 7267370389, 5631756169, 5928757429, 6485676974, 8108335, "SRX10083156", "SRS8241172", "SRA1195246", "GEO", "Takaomi Sanda Lab, Cancer Science Institute, National University of Singapore", 1, 0.92297, null, 0.2138, null, 0.84218, null, 0.52396, null, 98, null, "B", null, "usable mapping rate", "illumina", "hiseq_era", "unknown", "cdna_unspecified", "unknown", "sc", "single_cell_droplet", "10x", null, "Singapore", "2021-02-11", "Undetermined", "Undetermined", "Cancer or Tumor", "Cancer or Tumor"], [63247, "SRR13693857", "SRX10083155", "SRS8241171", "SRP305927", "PRJNA701473", "Single cell RNA seq analysis for normal lymphocytes and IRF4 driven zebrafish tumors", "GSE166646", "Transcriptome Analysis", "Single cell RNA seq analysis was carried out for 1 normal sample from a control zebrafish line lck mCherry and 5 non tumor and 14 tumor samples from the IRF4 transgenic line lck IRF4.  Tumor cells were harvested from the animals with or without xxx p53 mutation at different time points of tumor development. Overall design: Human IRF4 gene was overexpressed together with mCherry under the zebrafish lck promoter.  Samples were harvested from control or IRF4 transgenic zebrafish lck IRF4 with or without xxx p53 mutation. mCherry positive cells sorted by flow cytometry.  Normal cells was prepared from a control zebrafish which overexpresses only mCherry.  Single cell RNA seq analysis was performed by 10X Genomics using three prime Chromium Single Cell Technique.", "parent bioproject:PRJNA701471", "pubmed:35504924", null, "Tumor cells  Late stage  Ick:IRF4 fish 3 scRNA Seq", "GSM5076945", null, "source name:Zebrafish cells  transgenic|tissue:tumors driven by overexpression of human IRF4|sorted cells:mCherry sorted cells|genotype:IRF4 overexpression|time:Late stage", "Tumor cells  Late stage  Ick:IRF4 fish 3 scRNA Seq", "Annotations from Ensembl GRCz11 for zebrafish genes and transcripts were used and concatenated with mCherry and human IRF4 ENSG00000137265 gene information.  Single cell data were generated using mkref from cellranger package. Alignment  barcode assignation  and generation of cell gene count matrices were all performed using cellranger count from 10x genomics version 3.1.0 cellranger count   id zv11 {sampleID}   fastqs={directory scSeq}   sample={sampleID}  transcriptome={mkgtf generated STAR library} Genome build: GRCz11 Danio Rerio + mCherry + Human IRF4 ENSG00000137265 Supplementary files format and content: HDF5 Gene Barcode Matrix format containing UMI counts of each gene for individual cells.  The data files can be deconvoluted to tsv and mtx files using cellranger reanalyze", "Zebrafish cells  transgenic", "No treatment", "post sorting  the cells were washed and processed for barcoding using the 10x Genomics Chromium Single Cell three prime Solution v2 kit following manufacturer's instructions. Illumina P5 and P7 sequences and sample index sequences are added during the Sample Index PCR. The final library fragments contain the P5  P7  Read 1 and Read 2 sequences used in Illumina bridge amplification and sequencing. Additionally  each fragment contains the 10x Barcode  UMI and cDNA insert sequence used in data analysis. Single cell RNA Seq", "The human IRF4 gene and mCherry fluorescent marker gene were transduced under the zebrafish lck promoter in zebrafish.  post the development of lymphoma phenotype  tumor cells were harvested and sorted by flow cytometry based on mCherry fluorescence expression.  A zebrafish which was transduced only with mCherry was used as a control.", "tissue:tumors driven by overexpression of human IRF4|sorted cells:mCherry sorted cells|genotype:IRF4 overexpression|time:Late stage", "GSM5076945", "GSM5076945: Tumor cells  Late stage  Ick:IRF4 fish 3 scRNA Seq; Danio rerio; RNA Seq", "GSM5076945", null, "1", "post sorting  the cells were washed and processed for barcoding using the 10x Genomics Chromium Single Cell three prime Solution v2 kit following manufacturer's instructions. Illumina P5 and P7 sequences and sample index sequences are added during the Sample Index PCR. The final library fragments contain the P5  P7  Read 1 and Read 2 sequences used in Illumina bridge amplification and sequencing. Additionally  each fragment contains the 10x Barcode  UMI and cDNA insert sequence used in data analysis. Single cell RNA Seq", "GEO Accession:GSM5076945", "RNA-Seq", "TRANSCRIPTOMIC", "cDNA", "PAIRED", "ILLUMINA", "HiSeq X Ten", null, "SRP305927", null, "loader:fastq load.py|options:  platform=Illumina   readTypes=TTB   read1PairFiles=10G I1.fastq.gz   read2PairFiles=10G R1.fastq.gz   read3PairFiles=10G R2.fastq.gz", null, null, 29362596648.0, 222443914.0, "GSM5076945 r1", "0:8 1:26 2:98", "A:8309910202;C:6578384206;G:7008276151;T:7440260771;N:25765318", 8, 26, 98, null, 8309910202, 6578384206, 7008276151, 7440260771, 25765318, "SRX10083155", "SRS8241171", "SRA1195246", "GEO", "Takaomi Sanda Lab, Cancer Science Institute, National University of Singapore", 1, 0.92108, null, 0.20892, null, 0.85484, null, 0.52156, null, 98, null, "B", null, "usable mapping rate", "illumina", "hiseq_era", "unknown", "cdna_unspecified", "unknown", "sc", "single_cell_droplet", "10x", null, "Singapore", "2021-02-11", "Undetermined", "Undetermined", "Cancer or Tumor", "Cancer or Tumor"], [63248, "SRR13693856", "SRX10083154", "SRS8241170", "SRP305927", "PRJNA701473", "Single cell RNA seq analysis for normal lymphocytes and IRF4 driven zebrafish tumors", "GSE166646", "Transcriptome Analysis", "Single cell RNA seq analysis was carried out for 1 normal sample from a control zebrafish line lck mCherry and 5 non tumor and 14 tumor samples from the IRF4 transgenic line lck IRF4.  Tumor cells were harvested from the animals with or without xxx p53 mutation at different time points of tumor development. Overall design: Human IRF4 gene was overexpressed together with mCherry under the zebrafish lck promoter.  Samples were harvested from control or IRF4 transgenic zebrafish lck IRF4 with or without xxx p53 mutation. mCherry positive cells sorted by flow cytometry.  Normal cells was prepared from a control zebrafish which overexpresses only mCherry.  Single cell RNA seq analysis was performed by 10X Genomics using three prime Chromium Single Cell Technique.", "parent bioproject:PRJNA701471", "pubmed:35504924", null, "Tumor cells  Late stage  Ick:IRF4 fish 2 scRNA Seq", "GSM5076944", null, "source name:Zebrafish cells  transgenic|tissue:tumors driven by overexpression of human IRF4|sorted cells:mCherry sorted cells|genotype:IRF4 overexpression|time:Late stage", "Tumor cells  Late stage  Ick:IRF4 fish 2 scRNA Seq", "Annotations from Ensembl GRCz11 for zebrafish genes and transcripts were used and concatenated with mCherry and human IRF4 ENSG00000137265 gene information.  Single cell data were generated using mkref from cellranger package. Alignment  barcode assignation  and generation of cell gene count matrices were all performed using cellranger count from 10x genomics version 3.1.0 cellranger count   id zv11 {sampleID}   fastqs={directory scSeq}   sample={sampleID}  transcriptome={mkgtf generated STAR library} Genome build: GRCz11 Danio Rerio + mCherry + Human IRF4 ENSG00000137265 Supplementary files format and content: HDF5 Gene Barcode Matrix format containing UMI counts of each gene for individual cells.  The data files can be deconvoluted to tsv and mtx files using cellranger reanalyze", "Zebrafish cells  transgenic", "No treatment", "post sorting  the cells were washed and processed for barcoding using the 10x Genomics Chromium Single Cell three prime Solution v2 kit following manufacturer's instructions. Illumina P5 and P7 sequences and sample index sequences are added during the Sample Index PCR. The final library fragments contain the P5  P7  Read 1 and Read 2 sequences used in Illumina bridge amplification and sequencing. Additionally  each fragment contains the 10x Barcode  UMI and cDNA insert sequence used in data analysis. Single cell RNA Seq", "The human IRF4 gene and mCherry fluorescent marker gene were transduced under the zebrafish lck promoter in zebrafish.  post the development of lymphoma phenotype  tumor cells were harvested and sorted by flow cytometry based on mCherry fluorescence expression.  A zebrafish which was transduced only with mCherry was used as a control.", "tissue:tumors driven by overexpression of human IRF4|sorted cells:mCherry sorted cells|genotype:IRF4 overexpression|time:Late stage", "GSM5076944", "GSM5076944: Tumor cells  Late stage  Ick:IRF4 fish 2 scRNA Seq; Danio rerio; RNA Seq", "GSM5076944", null, "1", "post sorting  the cells were washed and processed for barcoding using the 10x Genomics Chromium Single Cell three prime Solution v2 kit following manufacturer's instructions. Illumina P5 and P7 sequences and sample index sequences are added during the Sample Index PCR. The final library fragments contain the P5  P7  Read 1 and Read 2 sequences used in Illumina bridge amplification and sequencing. Additionally  each fragment contains the 10x Barcode  UMI and cDNA insert sequence used in data analysis. Single cell RNA Seq", "GEO Accession:GSM5076944", "RNA-Seq", "TRANSCRIPTOMIC", "cDNA", "PAIRED", "ILLUMINA", "HiSeq X Ten", null, "SRP305927", null, "loader:fastq load.py|options:  platform=Illumina   readTypes=TTB   read1PairFiles=10F I1.fastq.gz   read2PairFiles=10F R1.fastq.gz   read3PairFiles=10F R2.fastq.gz", "10F_I1.fastq.gz 10F_R1.fastq.gz 10F_R2.fastq.gz", "fastq fastq fastq", 30225931824.0, 228984332.0, "GSM5076944 r1", "0:8 1:26 2:98", "A:8484220529;C:6779948314;G:7231863744;T:7703283562;N:26615675", 8, 26, 98, null, 8484220529, 6779948314, 7231863744, 7703283562, 26615675, "SRX10083154", "SRS8241170", "SRA1195246", "GEO", "Takaomi Sanda Lab, Cancer Science Institute, National University of Singapore", 1, 0.92746, null, 0.1895, null, 0.85817, null, 0.49147, null, 98, null, "B", null, "usable mapping rate", "illumina", "hiseq_era", "unknown", "cdna_unspecified", "unknown", "sc", "single_cell_droplet", "10x", null, "Singapore", "2021-02-11", "Undetermined", "Undetermined", "Cancer or Tumor", "Cancer or Tumor"], [63249, "SRR13693855", "SRX10083153", "SRS8241169", "SRP305927", "PRJNA701473", "Single cell RNA seq analysis for normal lymphocytes and IRF4 driven zebrafish tumors", "GSE166646", "Transcriptome Analysis", "Single cell RNA seq analysis was carried out for 1 normal sample from a control zebrafish line lck mCherry and 5 non tumor and 14 tumor samples from the IRF4 transgenic line lck IRF4.  Tumor cells were harvested from the animals with or without xxx p53 mutation at different time points of tumor development. Overall design: Human IRF4 gene was overexpressed together with mCherry under the zebrafish lck promoter.  Samples were harvested from control or IRF4 transgenic zebrafish lck IRF4 with or without xxx p53 mutation. mCherry positive cells sorted by flow cytometry.  Normal cells was prepared from a control zebrafish which overexpresses only mCherry.  Single cell RNA seq analysis was performed by 10X Genomics using three prime Chromium Single Cell Technique.", "parent bioproject:PRJNA701471", "pubmed:35504924", null, "Tumor cells  Late stage  Ick:IRF4 fish 1 scRNA Seq", "GSM5076943", null, "source name:Zebrafish cells  transgenic|tissue:tumors driven by overexpression of human IRF4|sorted cells:mCherry sorted cells|genotype:IRF4 overexpression|time:Late stage", "Tumor cells  Late stage  Ick:IRF4 fish 1 scRNA Seq", "Annotations from Ensembl GRCz11 for zebrafish genes and transcripts were used and concatenated with mCherry and human IRF4 ENSG00000137265 gene information.  Single cell data were generated using mkref from cellranger package. Alignment  barcode assignation  and generation of cell gene count matrices were all performed using cellranger count from 10x genomics version 3.1.0 cellranger count   id zv11 {sampleID}   fastqs={directory scSeq}   sample={sampleID}  transcriptome={mkgtf generated STAR library} Genome build: GRCz11 Danio Rerio + mCherry + Human IRF4 ENSG00000137265 Supplementary files format and content: HDF5 Gene Barcode Matrix format containing UMI counts of each gene for individual cells.  The data files can be deconvoluted to tsv and mtx files using cellranger reanalyze", "Zebrafish cells  transgenic", "No treatment", "post sorting  the cells were washed and processed for barcoding using the 10x Genomics Chromium Single Cell three prime Solution v2 kit following manufacturer's instructions. Illumina P5 and P7 sequences and sample index sequences are added during the Sample Index PCR. The final library fragments contain the P5  P7  Read 1 and Read 2 sequences used in Illumina bridge amplification and sequencing. Additionally  each fragment contains the 10x Barcode  UMI and cDNA insert sequence used in data analysis. Single cell RNA Seq", "The human IRF4 gene and mCherry fluorescent marker gene were transduced under the zebrafish lck promoter in zebrafish.  post the development of lymphoma phenotype  tumor cells were harvested and sorted by flow cytometry based on mCherry fluorescence expression.  A zebrafish which was transduced only with mCherry was used as a control.", "tissue:tumors driven by overexpression of human IRF4|sorted cells:mCherry sorted cells|genotype:IRF4 overexpression|time:Late stage", "GSM5076943", "GSM5076943: Tumor cells  Late stage  Ick:IRF4 fish 1 scRNA Seq; Danio rerio; RNA Seq", "GSM5076943", null, "1", "post sorting  the cells were washed and processed for barcoding using the 10x Genomics Chromium Single Cell three prime Solution v2 kit following manufacturer's instructions. Illumina P5 and P7 sequences and sample index sequences are added during the Sample Index PCR. The final library fragments contain the P5  P7  Read 1 and Read 2 sequences used in Illumina bridge amplification and sequencing. Additionally  each fragment contains the 10x Barcode  UMI and cDNA insert sequence used in data analysis. Single cell RNA Seq", "GEO Accession:GSM5076943", "RNA-Seq", "TRANSCRIPTOMIC", "cDNA", "PAIRED", "ILLUMINA", "HiSeq X Ten", null, "SRP305927", null, "loader:fastq load.py|options:  platform=Illumina   readTypes=TTB   read1PairFiles=10E I1.fastq.gz   read2PairFiles=10E R1.fastq.gz   read3PairFiles=10E R2.fastq.gz", "10E_I1.fastq 10E_R1.fastq 10E_R2.fastq", "fastq fastq fastq", 34321213080.0, 260009190.0, "GSM5076943 r1", "0:8 1:26 2:98", "A:9548435346;C:7827936248;G:8159132985;T:8755456452;N:30252049", 8, 26, 98, null, 9548435346, 7827936248, 8159132985, 8755456452, 30252049, "SRX10083153", "SRS8241169", "SRA1195246", "GEO", "Takaomi Sanda Lab, Cancer Science Institute, National University of Singapore", 1, 0.92658, null, 0.1882, null, 0.84861, null, 0.50119, null, 98, null, "B", null, "usable mapping rate", "illumina", "hiseq_era", "unknown", "cdna_unspecified", "unknown", "sc", "single_cell_droplet", "10x", null, "Singapore", "2021-02-11", "Undetermined", "Undetermined", "Cancer or Tumor", "Cancer or Tumor"], [63250, "SRR13693854", "SRX10083152", "SRS8241168", "SRP305927", "PRJNA701473", "Single cell RNA seq analysis for normal lymphocytes and IRF4 driven zebrafish tumors", "GSE166646", "Transcriptome Analysis", "Single cell RNA seq analysis was carried out for 1 normal sample from a control zebrafish line lck mCherry and 5 non tumor and 14 tumor samples from the IRF4 transgenic line lck IRF4.  Tumor cells were harvested from the animals with or without xxx p53 mutation at different time points of tumor development. Overall design: Human IRF4 gene was overexpressed together with mCherry under the zebrafish lck promoter.  Samples were harvested from control or IRF4 transgenic zebrafish lck IRF4 with or without xxx p53 mutation. mCherry positive cells sorted by flow cytometry.  Normal cells was prepared from a control zebrafish which overexpresses only mCherry.  Single cell RNA seq analysis was performed by 10X Genomics using three prime Chromium Single Cell Technique.", "parent bioproject:PRJNA701471", "pubmed:35504924", null, "Tumor cells  Early stage  Ick:IRF4 fish 3 scRNA Seq", "GSM5076942", null, "source name:Zebrafish cells  transgenic|tissue:tumors driven by overexpression of human IRF4|sorted cells:mCherry sorted cells|genotype:IRF4 overexpression|time:Early stage", "Tumor cells  Early stage  Ick:IRF4 fish 3 scRNA Seq", "Annotations from Ensembl GRCz11 for zebrafish genes and transcripts were used and concatenated with mCherry and human IRF4 ENSG00000137265 gene information.  Single cell data were generated using mkref from cellranger package. Alignment  barcode assignation  and generation of cell gene count matrices were all performed using cellranger count from 10x genomics version 3.1.0 cellranger count   id zv11 {sampleID}   fastqs={directory scSeq}   sample={sampleID}  transcriptome={mkgtf generated STAR library} Genome build: GRCz11 Danio Rerio + mCherry + Human IRF4 ENSG00000137265 Supplementary files format and content: HDF5 Gene Barcode Matrix format containing UMI counts of each gene for individual cells.  The data files can be deconvoluted to tsv and mtx files using cellranger reanalyze", "Zebrafish cells  transgenic", "No treatment", "post sorting  the cells were washed and processed for barcoding using the 10x Genomics Chromium Single Cell three prime Solution v2 kit following manufacturer's instructions. Illumina P5 and P7 sequences and sample index sequences are added during the Sample Index PCR. The final library fragments contain the P5  P7  Read 1 and Read 2 sequences used in Illumina bridge amplification and sequencing. Additionally  each fragment contains the 10x Barcode  UMI and cDNA insert sequence used in data analysis. Single cell RNA Seq", "The human IRF4 gene and mCherry fluorescent marker gene were transduced under the zebrafish lck promoter in zebrafish.  post the development of lymphoma phenotype  tumor cells were harvested and sorted by flow cytometry based on mCherry fluorescence expression.  A zebrafish which was transduced only with mCherry was used as a control.", "tissue:tumors driven by overexpression of human IRF4|sorted cells:mCherry sorted cells|genotype:IRF4 overexpression|time:Early stage", "GSM5076942", "GSM5076942: Tumor cells  Early stage  Ick:IRF4 fish 3 scRNA Seq; Danio rerio; RNA Seq", "GSM5076942", null, "1", "post sorting  the cells were washed and processed for barcoding using the 10x Genomics Chromium Single Cell three prime Solution v2 kit following manufacturer's instructions. Illumina P5 and P7 sequences and sample index sequences are added during the Sample Index PCR. The final library fragments contain the P5  P7  Read 1 and Read 2 sequences used in Illumina bridge amplification and sequencing. Additionally  each fragment contains the 10x Barcode  UMI and cDNA insert sequence used in data analysis. Single cell RNA Seq", "GEO Accession:GSM5076942", "RNA-Seq", "TRANSCRIPTOMIC", "cDNA", "PAIRED", "ILLUMINA", "HiSeq X Ten", null, "SRP305927", null, "loader:fastq load.py|options:  platform=Illumina   readTypes=TTB   read1PairFiles=3D I1.fastq.gz   read2PairFiles=3D R1.fastq.gz   read3PairFiles=3D R2.fastq.gz", "3D_I1.fastq 3D_R1.fastq 3D_R2.fastq", "fastq fastq fastq", 29652167556.0, 224637633.0, "GSM5076942 r1", "0:8 1:26 2:98", "A:8364846981;C:6574443334;G:6910197942;T:7776537448;N:26141851", 8, 26, 98, null, 8364846981, 6574443334, 6910197942, 7776537448, 26141851, "SRX10083152", "SRS8241168", "SRA1195246", "GEO", "Takaomi Sanda Lab, Cancer Science Institute, National University of Singapore", 1, 0.91807, null, 0.19059, null, 0.83205, null, 0.56087, null, 98, null, "B", null, "usable mapping rate", "illumina", "hiseq_era", "unknown", "cdna_unspecified", "unknown", "sc", "single_cell_droplet", "10x", null, "Singapore", "2021-02-11", "Undetermined", "Undetermined", "Cancer or Tumor", "Cancer or Tumor"], [63251, "SRR13693853", "SRX10083151", "SRS8241167", "SRP305927", "PRJNA701473", "Single cell RNA seq analysis for normal lymphocytes and IRF4 driven zebrafish tumors", "GSE166646", "Transcriptome Analysis", "Single cell RNA seq analysis was carried out for 1 normal sample from a control zebrafish line lck mCherry and 5 non tumor and 14 tumor samples from the IRF4 transgenic line lck IRF4.  Tumor cells were harvested from the animals with or without xxx p53 mutation at different time points of tumor development. Overall design: Human IRF4 gene was overexpressed together with mCherry under the zebrafish lck promoter.  Samples were harvested from control or IRF4 transgenic zebrafish lck IRF4 with or without xxx p53 mutation. mCherry positive cells sorted by flow cytometry.  Normal cells was prepared from a control zebrafish which overexpresses only mCherry.  Single cell RNA seq analysis was performed by 10X Genomics using three prime Chromium Single Cell Technique.", "parent bioproject:PRJNA701471", "pubmed:35504924", null, "Tumor cells  Early stage  Ick:IRF4 fish 2 scRNA Seq", "GSM5076941", null, "source name:Zebrafish cells  transgenic|tissue:tumors driven by overexpression of human IRF4|sorted cells:mCherry sorted cells|genotype:IRF4 overexpression|time:Early stage", "Tumor cells  Early stage  Ick:IRF4 fish 2 scRNA Seq", "Annotations from Ensembl GRCz11 for zebrafish genes and transcripts were used and concatenated with mCherry and human IRF4 ENSG00000137265 gene information.  Single cell data were generated using mkref from cellranger package. Alignment  barcode assignation  and generation of cell gene count matrices were all performed using cellranger count from 10x genomics version 3.1.0 cellranger count   id zv11 {sampleID}   fastqs={directory scSeq}   sample={sampleID}  transcriptome={mkgtf generated STAR library} Genome build: GRCz11 Danio Rerio + mCherry + Human IRF4 ENSG00000137265 Supplementary files format and content: HDF5 Gene Barcode Matrix format containing UMI counts of each gene for individual cells.  The data files can be deconvoluted to tsv and mtx files using cellranger reanalyze", "Zebrafish cells  transgenic", "No treatment", "post sorting  the cells were washed and processed for barcoding using the 10x Genomics Chromium Single Cell three prime Solution v2 kit following manufacturer's instructions. Illumina P5 and P7 sequences and sample index sequences are added during the Sample Index PCR. The final library fragments contain the P5  P7  Read 1 and Read 2 sequences used in Illumina bridge amplification and sequencing. Additionally  each fragment contains the 10x Barcode  UMI and cDNA insert sequence used in data analysis. Single cell RNA Seq", "The human IRF4 gene and mCherry fluorescent marker gene were transduced under the zebrafish lck promoter in zebrafish.  post the development of lymphoma phenotype  tumor cells were harvested and sorted by flow cytometry based on mCherry fluorescence expression.  A zebrafish which was transduced only with mCherry was used as a control.", "tissue:tumors driven by overexpression of human IRF4|sorted cells:mCherry sorted cells|genotype:IRF4 overexpression|time:Early stage", "GSM5076941", "GSM5076941: Tumor cells  Early stage  Ick:IRF4 fish 2 scRNA Seq; Danio rerio; RNA Seq", "GSM5076941", null, "1", "post sorting  the cells were washed and processed for barcoding using the 10x Genomics Chromium Single Cell three prime Solution v2 kit following manufacturer's instructions. Illumina P5 and P7 sequences and sample index sequences are added during the Sample Index PCR. The final library fragments contain the P5  P7  Read 1 and Read 2 sequences used in Illumina bridge amplification and sequencing. Additionally  each fragment contains the 10x Barcode  UMI and cDNA insert sequence used in data analysis. Single cell RNA Seq", "GEO Accession:GSM5076941", "RNA-Seq", "TRANSCRIPTOMIC", "cDNA", "PAIRED", "ILLUMINA", "HiSeq X Ten", null, "SRP305927", null, "loader:fastq load.py|options:  platform=Illumina   readTypes=TTB   read1PairFiles=3C I1.fastq.gz   read2PairFiles=3C R1.fastq.gz   read3PairFiles=3C R2.fastq.gz", "3C_I1.fastq.gz 3C_R1.fastq.gz 3C_R2.fastq.gz", "fastq fastq fastq", 29997585156.0, 227254433.0, "GSM5076941 r1", "0:8 1:26 2:98", "A:8572344693;C:6580024899;G:7240023287;T:7578830064;N:26362213", 8, 26, 98, null, 8572344693, 6580024899, 7240023287, 7578830064, 26362213, "SRX10083151", "SRS8241167", "SRA1195246", "GEO", "Takaomi Sanda Lab, Cancer Science Institute, National University of Singapore", 1, 0.93097, null, 0.27389, null, 0.86318, null, 0.50798, null, 98, null, "B", null, "usable mapping rate", "illumina", "hiseq_era", "unknown", "cdna_unspecified", "unknown", "sc", "single_cell_droplet", "10x", null, "Singapore", "2021-02-11", "Undetermined", "Undetermined", "Cancer or Tumor", "Cancer or Tumor"], [63252, "SRR13693852", "SRX10083150", "SRS8241166", "SRP305927", "PRJNA701473", "Single cell RNA seq analysis for normal lymphocytes and IRF4 driven zebrafish tumors", "GSE166646", "Transcriptome Analysis", "Single cell RNA seq analysis was carried out for 1 normal sample from a control zebrafish line lck mCherry and 5 non tumor and 14 tumor samples from the IRF4 transgenic line lck IRF4.  Tumor cells were harvested from the animals with or without xxx p53 mutation at different time points of tumor development. Overall design: Human IRF4 gene was overexpressed together with mCherry under the zebrafish lck promoter.  Samples were harvested from control or IRF4 transgenic zebrafish lck IRF4 with or without xxx p53 mutation. mCherry positive cells sorted by flow cytometry.  Normal cells was prepared from a control zebrafish which overexpresses only mCherry.  Single cell RNA seq analysis was performed by 10X Genomics using three prime Chromium Single Cell Technique.", "parent bioproject:PRJNA701471", "pubmed:35504924", null, "Tumor cells  Early stage  Ick:IRF4 fish 1 scRNA Seq", "GSM5076940", null, "source name:Zebrafish cells  transgenic|tissue:tumors driven by overexpression of human IRF4|sorted cells:mCherry sorted cells|genotype:IRF4 overexpression|time:Early stage", "Tumor cells  Early stage  Ick:IRF4 fish 1 scRNA Seq", "Annotations from Ensembl GRCz11 for zebrafish genes and transcripts were used and concatenated with mCherry and human IRF4 ENSG00000137265 gene information.  Single cell data were generated using mkref from cellranger package. Alignment  barcode assignation  and generation of cell gene count matrices were all performed using cellranger count from 10x genomics version 3.1.0 cellranger count   id zv11 {sampleID}   fastqs={directory scSeq}   sample={sampleID}  transcriptome={mkgtf generated STAR library} Genome build: GRCz11 Danio Rerio + mCherry + Human IRF4 ENSG00000137265 Supplementary files format and content: HDF5 Gene Barcode Matrix format containing UMI counts of each gene for individual cells.  The data files can be deconvoluted to tsv and mtx files using cellranger reanalyze", "Zebrafish cells  transgenic", "No treatment", "post sorting  the cells were washed and processed for barcoding using the 10x Genomics Chromium Single Cell three prime Solution v2 kit following manufacturer's instructions. Illumina P5 and P7 sequences and sample index sequences are added during the Sample Index PCR. The final library fragments contain the P5  P7  Read 1 and Read 2 sequences used in Illumina bridge amplification and sequencing. Additionally  each fragment contains the 10x Barcode  UMI and cDNA insert sequence used in data analysis. Single cell RNA Seq", "The human IRF4 gene and mCherry fluorescent marker gene were transduced under the zebrafish lck promoter in zebrafish.  post the development of lymphoma phenotype  tumor cells were harvested and sorted by flow cytometry based on mCherry fluorescence expression.  A zebrafish which was transduced only with mCherry was used as a control.", "tissue:tumors driven by overexpression of human IRF4|sorted cells:mCherry sorted cells|genotype:IRF4 overexpression|time:Early stage", "GSM5076940", "GSM5076940: Tumor cells  Early stage  Ick:IRF4 fish 1 scRNA Seq; Danio rerio; RNA Seq", "GSM5076940", null, "1", "post sorting  the cells were washed and processed for barcoding using the 10x Genomics Chromium Single Cell three prime Solution v2 kit following manufacturer's instructions. Illumina P5 and P7 sequences and sample index sequences are added during the Sample Index PCR. The final library fragments contain the P5  P7  Read 1 and Read 2 sequences used in Illumina bridge amplification and sequencing. Additionally  each fragment contains the 10x Barcode  UMI and cDNA insert sequence used in data analysis. Single cell RNA Seq", "GEO Accession:GSM5076940", "RNA-Seq", "TRANSCRIPTOMIC", "cDNA", "PAIRED", "ILLUMINA", "HiSeq X Ten", null, "SRP305927", null, "loader:fastq load.py|options:  platform=Illumina   readTypes=TTB   read1PairFiles=3A I1.fastq.gz   read2PairFiles=3A R1.fastq.gz   read3PairFiles=3A R2.fastq.gz", null, null, 29170933836.0, 220991923.0, "GSM5076940 r1", "0:8 1:26 2:98", "A:8114837766;C:6514920127;G:6820788482;T:7694661638;N:25725823", 8, 26, 98, null, 8114837766, 6514920127, 6820788482, 7694661638, 25725823, "SRX10083150", "SRS8241166", "SRA1195246", "GEO", "Takaomi Sanda Lab, Cancer Science Institute, National University of Singapore", 1, 0.91826, null, 0.16532, null, 0.82755, null, 0.51956, null, 98, null, "B", null, "usable mapping rate", "illumina", "hiseq_era", "unknown", "cdna_unspecified", "unknown", "sc", "single_cell_droplet", "10x", null, "Singapore", "2021-02-11", "Undetermined", "Undetermined", "Cancer or Tumor", "Cancer or Tumor"]], "truncated": false, "filtered_table_rows_count": 23, "expanded_columns": [], "expandable_columns": [], "columns": ["rowid", "run.accession", "experiment.accession", "sample.accession", "study.accession", "bioproject", "study.title", "study.alias", "study.type", "study.abstract", "study.attributes", "study.PMIDs", "sample.description", "sample.title", "sample.alias", "sample.centername", "sample.attributes", "GEOsample.title", "GEOsample.dataprocessing", "GEOsample.source", "GEOsample.treatmentprotocol", "GEOsample.extractprotocol", "GEOsample.growthprotocol", "GEOsample.characteristics", "GEOsample.accession", "experiment.title", "experiment.alias", "experiment.library_name", "experiment.design_description", "experiment.library_construction_protocol", "experiment.attributes", "experiment.library_strategy", "experiment.library_source", "experiment.library_selection", "experiment.library_layout", "experiment.platform", "experiment.instrument_model", "experiment.spot_descriptor", "experiment.study_ref", 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"technology", "tech_variant", "submission.bioprojectsource.country", "earliest_date", "devstage_curation", "devstage_curation_coarse", "tissue_curation", "tissue_curation_coarse"], "primary_keys": [], "units": {}, "query": {"sql": "select rowid, [run.accession], [experiment.accession], [sample.accession], [study.accession], bioproject, [study.title], [study.alias], [study.type], [study.abstract], [study.attributes], [study.PMIDs], [sample.description], [sample.title], [sample.alias], [sample.centername], [sample.attributes], [GEOsample.title], [GEOsample.dataprocessing], [GEOsample.source], [GEOsample.treatmentprotocol], [GEOsample.extractprotocol], [GEOsample.growthprotocol], [GEOsample.characteristics], [GEOsample.accession], [experiment.title], [experiment.alias], [experiment.library_name], [experiment.design_description], [experiment.library_construction_protocol], [experiment.attributes], [experiment.library_strategy], [experiment.library_source], [experiment.library_selection], [experiment.library_layout], [experiment.platform], [experiment.instrument_model], [experiment.spot_descriptor], [experiment.study_ref], [run.title], [run.attributes], [run.filename], [run.semantic_name], [run.total_bases], [run.total_spots], [run.alias], [run.read_lengths], [run.base_counts], [run.r1_length], [run.r2_length], [run.r3_length], [run.r4_length], [run.Acount], [run.Ccount], [run.Gcount], [run.Tcount], [run.Ncount], [run.experiment], [run.pool_member], [submission.accession], [submission.srasource], [submission.bioprojectsource], [seqdetective.n_mates], [seqdetective.mapping_rate.mate1], [seqdetective.mapping_rate.mate2], [seqdetective.nofeature_rate.mate1], [seqdetective.nofeature_rate.mate2], [seqdetective.sparsity.mate1], [seqdetective.sparsity.mate2], [seqdetective.pos_strand_rate.mate1], [seqdetective.pos_strand_rate.mate2], [seqdetective.readlen.mate1], [seqdetective.readlen.mate2], [seqdetective.judgement.mate1], [seqdetective.judgement.mate2], 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