run_metadata
6 rows where devstage_curation = "Multi-stage" and tissue_curation_coarse = "Embryo Imprecise"
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| Link | 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 | seqdetective.judgement.reason | platform_family | instrument_generation | read_bias | selection_class | prep_kit | sc_or_bulk | tech_class | technology | tech_variant | submission.bioprojectsource.country | earliest_date | devstage_curation | devstage_curation_coarse | tissue_curation | tissue_curation_coarse |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 10213 | 10213 | ERR6511329 | ERX6138165 | ERS7264188 | ERP131213 | PRJEB46978 | Nano3P seq: transcriptome wide analysis of gene expression and tail dynamics using end capture nanopore sequencing | ena-STUDY-CENTER FOR GENOMIC REGULATION (CRG)-12-08-2021-14:48:52:906-1159 | Other | Nano3P seq is a simple and robust method to accurately estimate transcript levels tail lengths and tail nucleotide composition information in full length individual reads with minimal library preparation biases both in the coding and non coding transcriptome. | ENA FIRST PUBLIC:2023 12 28|ENA LAST UPDATE:2023 12 28 | Zebrafish Nano3P seq of Ribodepleted sample biological replicate 1 including 2 hpf 4 hpf 6 hpf RNAs | Zebrafish Ribodep Rep1 | SAMEA9541418 | CENTER FOR GENOMIC REGULATION (CRG) | ENA FIRST PUBLIC:2023 12 28T01:07:23Z|ENA LAST UPDATE:2023 12 28T01:07:23Z|External Id:SAMEA9541418|INSDC center name:CENTER FOR GENOMIC REGULATION CRG|INSDC first public:2023 12 28T01:07:23Z|INSDC last update:2023 12 28T01:07:23Z|INSDC status:public|Submitter Id:Zebrafish Ribodep Rep1|common name:zebrafish|sample name:Zebrafish Ribodep Rep1|scientific name:Danio rerio | MinION sequencing | ena EXPERIMENT CENTER FOR GENOMIC REGULATION CRG 17 08 2021 13:09:55:665 3 | cDNA786327 | Nano3P seq | Nano3P seq | OTHER | TRANSCRIPTOMIC | unspecified | SINGLE | OXFORD_NANOPORE | MinION | ERP131213 | MinION sequencing | ENA FIRST PUBLIC:2023 12 28|ENA LAST UPDATE:2023 12 28 | zebrafish_ribodep_rep1.tar.gz | nanopore | 1745399583.0 | 1644167.0 | ena RUN CENTER FOR GENOMIC REGULATION CRG 17 08 2021 13:09:55:665 3 | 0:1061.57 | A:449704009;C:421915878;G:378879857;T:494899839;N:0 | 1061 | 449704009 | 421915878 | 378879857 | 494899839 | 0 | ERX6138165 | ERS7264188 | ERA5757997 | CENTER FOR GENOMIC REGULATION (CRG)|European Nucleotide Archive | CENTER FOR GENOMIC REGULATION (CRG) | 1 | 0.01112 | 0.0 | 0.99997 | 1.0 | 546 | T | long read | ont | ont | full_length | rrna_depletion | unknown | bulk | unknown | unknown | Spain | 2023-12-28 | Multi-stage | Embryo | Undetermined | Embryo Imprecise | |||||||||||||||||||||
| 10215 | 10215 | ERR6511330 | ERX6138166 | ERS7264189 | ERP131213 | PRJEB46978 | Nano3P seq: transcriptome wide analysis of gene expression and tail dynamics using end capture nanopore sequencing | ena-STUDY-CENTER FOR GENOMIC REGULATION (CRG)-12-08-2021-14:48:52:906-1159 | Other | Nano3P seq is a simple and robust method to accurately estimate transcript levels tail lengths and tail nucleotide composition information in full length individual reads with minimal library preparation biases both in the coding and non coding transcriptome. | ENA FIRST PUBLIC:2023 12 28|ENA LAST UPDATE:2023 12 28 | Zebrafish Nano3P seq of Ribodepleted sample biological replicate 1 including 2 hpf 4 hpf 6 hpf RNAs | Zebrafish Ribodep Rep2 | SAMEA9541419 | CENTER FOR GENOMIC REGULATION (CRG) | ENA FIRST PUBLIC:2023 12 28T01:07:23Z|ENA LAST UPDATE:2023 12 28T01:07:23Z|External Id:SAMEA9541419|INSDC center name:CENTER FOR GENOMIC REGULATION CRG|INSDC first public:2023 12 28T01:07:23Z|INSDC last update:2023 12 28T01:07:23Z|INSDC status:public|Submitter Id:Zebrafish Ribodep Rep2|common name:zebrafish|sample name:Zebrafish Ribodep Rep2|scientific name:Danio rerio | MinION sequencing | ena EXPERIMENT CENTER FOR GENOMIC REGULATION CRG 17 08 2021 13:09:55:665 4 | cDNA123791 | Nano3P seq | Nano3P seq | OTHER | TRANSCRIPTOMIC | unspecified | SINGLE | OXFORD_NANOPORE | MinION | ERP131213 | MinION sequencing | ENA FIRST PUBLIC:2023 12 28|ENA LAST UPDATE:2023 12 28 | zebrafish_ribodep_rep2.tar.gz | nanopore | 2038398139.0 | 1955617.0 | ena RUN CENTER FOR GENOMIC REGULATION CRG 17 08 2021 13:09:55:665 4 | 0:1042.33 | A:518369802;C:477535545;G:441294056;T:601198736;N:0 | 1042 | 518369802 | 477535545 | 441294056 | 601198736 | 0 | ERX6138166 | ERS7264189 | ERA5757997 | CENTER FOR GENOMIC REGULATION (CRG)|European Nucleotide Archive | CENTER FOR GENOMIC REGULATION (CRG) | ont | ont | full_length | rrna_depletion | unknown | bulk | unknown | unknown | Spain | 2023-12-28 | Multi-stage | Embryo | Undetermined | Embryo Imprecise | |||||||||||||||||||||||||||||
| 11042 | 11042 | ERR9839781 | ERX9385638 | ERS12199238 | ERP138294 | PRJEB53494 | Nano3P seq: transcriptome wide analysis of gene expression and tail dynamics using end capture nanopore cDNA sequencing | 94bf5509-4622-4d5f-b7c5-6a14bdfac340 | Other | RNA polyadenylation plays a central role in RNA maturation fate and stability. In response to developmental cues polyA tail lengths can vary affecting the translation efficiency and stability of mRNAs. Here we develop Nanopore three prime end capture sequencing Nano3P seq a novel method that relies on nanopore cDNA sequencing to simultaneously quantify RNA abundance tail composition and tail length dynamics at per read resolution. By employing a template switching based sequencing protocol Nano3P seq can sequence any given RNA molecule from its three prime end regardless of its polyadenylation status without xxx need for PCR amplification or ligation of RNA adapters. We demonstrate that Nano3P seq captures a wide diversity of RNA biotypes providing quantitative estimates of RNA abundance and tail lengths in mRNA lncRNA sn/snoRNA scaRNA and rRNA molecules. We find that in addition to mRNA and lncRNA polyA tails can be identified in 16S mitochondrial rRNA in both mouse and zebrafish models. Moreover we show that mRNA tail lengths are dynamically regulated during vertebrate embryogenesis at an isoform specific level correlating with mRNA decay. Finally we identify non A bases within polyA tails of various lengths and reveal their distribution during vertebrate embryogenesis. Overall Nano3P seq is a simple and robust method for accurately estimating transcript levels tail lengths and tail composition heterogeneity in individual reads with minimal library preparation biases both in the coding and non coding transcriptome. | ENA FIRST PUBLIC:2022 10 10|ENA LAST UPDATE:2022 10 10 | Zebrafish Ribodepleted RNA 2hpf 4hpf 6hpf | Zebrafish Ribodepleted Rep3 | SAMEA110100413 | CENTER FOR GENOMIC REGULATION (CRG) | ENA FIRST PUBLIC:2022 10 10|ENA LAST UPDATE:2022 10 10|External Id:SAMEA110100413|INSDC center alias:CENTER FOR GENOMIC REGULATION CRG|INSDC center name:CENTER FOR GENOMIC REGULATION CRG|INSDC first public:2022 10 10T00:20:53Z|INSDC last update:2022 10 10T00:20:53Z|INSDC status:public|Submitter Id:Zebrafish Ribodepleted Rep3|common name:zebrafish|sample name:Zebrafish Ribodepleted Rep3 | MinION sequencing | ena EXPERIMENT TAB 13 06 2022 16:07:52:807 817 | cDNA897892 ZFRDR3 | 1 | RNA-Seq | TRANSCRIPTOMIC | other | SINGLE | OXFORD_NANOPORE | MinION | ERP138294 | MinION sequencing | ENA FIRST PUBLIC:2022 10 10|ENA LAST UPDATE:2022 10 10 | cDNA897892_ZFRDR3.tar.gz | nanopore | 848659575.0 | 587586.0 | ena RUN TAB 13 06 2022 16:07:52:808 818 | 0:1444.32 | A:210205014;C:186527780;G:188214279;T:263712502;N:0 | 1444 | 210205014 | 186527780 | 188214279 | 263712502 | 0 | ERX9385638 | ERS12199238 | ERA15547404 | CENTER FOR GENOMIC REGULATION (CRG)|European Nucleotide Archive | CENTER FOR GENOMIC REGULATION (CRG) | ont | ont | 3prime | poly_a | unknown | bulk | unknown | unknown | Spain | 2022-10-10 | Multi-stage | Embryo | Undetermined | Embryo Imprecise | ||||||||||||||||||||||||||||||
| 11043 | 11043 | ERR9839780 | ERX9385637 | ERS12199237 | ERP138294 | PRJEB53494 | Nano3P seq: transcriptome wide analysis of gene expression and tail dynamics using end capture nanopore cDNA sequencing | 94bf5509-4622-4d5f-b7c5-6a14bdfac340 | Other | RNA polyadenylation plays a central role in RNA maturation fate and stability. In response to developmental cues polyA tail lengths can vary affecting the translation efficiency and stability of mRNAs. Here we develop Nanopore three prime end capture sequencing Nano3P seq a novel method that relies on nanopore cDNA sequencing to simultaneously quantify RNA abundance tail composition and tail length dynamics at per read resolution. By employing a template switching based sequencing protocol Nano3P seq can sequence any given RNA molecule from its three prime end regardless of its polyadenylation status without xxx need for PCR amplification or ligation of RNA adapters. We demonstrate that Nano3P seq captures a wide diversity of RNA biotypes providing quantitative estimates of RNA abundance and tail lengths in mRNA lncRNA sn/snoRNA scaRNA and rRNA molecules. We find that in addition to mRNA and lncRNA polyA tails can be identified in 16S mitochondrial rRNA in both mouse and zebrafish models. Moreover we show that mRNA tail lengths are dynamically regulated during vertebrate embryogenesis at an isoform specific level correlating with mRNA decay. Finally we identify non A bases within polyA tails of various lengths and reveal their distribution during vertebrate embryogenesis. Overall Nano3P seq is a simple and robust method for accurately estimating transcript levels tail lengths and tail composition heterogeneity in individual reads with minimal library preparation biases both in the coding and non coding transcriptome. | ENA FIRST PUBLIC:2022 10 10|ENA LAST UPDATE:2022 10 10 | Zebrafish Ribodepleted RNA 2hpf 4hpf 6hpf | Zebrafish Ribodepleted Rep2 | SAMEA110100412 | CENTER FOR GENOMIC REGULATION (CRG) | ENA FIRST PUBLIC:2022 10 10|ENA LAST UPDATE:2022 10 10|External Id:SAMEA110100412|INSDC center alias:CENTER FOR GENOMIC REGULATION CRG|INSDC center name:CENTER FOR GENOMIC REGULATION CRG|INSDC first public:2022 10 10T00:20:53Z|INSDC last update:2022 10 10T00:20:53Z|INSDC status:public|Submitter Id:Zebrafish Ribodepleted Rep2|common name:zebrafish|sample name:Zebrafish Ribodepleted Rep2 | MinION sequencing | ena EXPERIMENT TAB 13 06 2022 16:07:52:807 815 | cDNA123791 ZFRDR2 | 1 | RNA-Seq | TRANSCRIPTOMIC | other | SINGLE | OXFORD_NANOPORE | MinION | ERP138294 | MinION sequencing | ENA FIRST PUBLIC:2022 10 10|ENA LAST UPDATE:2022 10 10 | cDNA123791_ZFRDR2.tar.gz | nanopore | 2229275175.0 | 1955617.0 | ena RUN TAB 13 06 2022 16:07:52:807 816 | 0:1139.93 | A:533543922;C:498938137;G:515833119;T:680959997;N:0 | 1139 | 533543922 | 498938137 | 515833119 | 680959997 | 0 | ERX9385637 | ERS12199237 | ERA15547404 | CENTER FOR GENOMIC REGULATION (CRG)|European Nucleotide Archive | CENTER FOR GENOMIC REGULATION (CRG) | ont | ont | 3prime | poly_a | unknown | bulk | unknown | unknown | Spain | 2022-10-10 | Multi-stage | Embryo | Undetermined | Embryo Imprecise | ||||||||||||||||||||||||||||||
| 11044 | 11044 | ERR9839779 | ERX9385636 | ERS12199236 | ERP138294 | PRJEB53494 | Nano3P seq: transcriptome wide analysis of gene expression and tail dynamics using end capture nanopore cDNA sequencing | 94bf5509-4622-4d5f-b7c5-6a14bdfac340 | Other | RNA polyadenylation plays a central role in RNA maturation fate and stability. In response to developmental cues polyA tail lengths can vary affecting the translation efficiency and stability of mRNAs. Here we develop Nanopore three prime end capture sequencing Nano3P seq a novel method that relies on nanopore cDNA sequencing to simultaneously quantify RNA abundance tail composition and tail length dynamics at per read resolution. By employing a template switching based sequencing protocol Nano3P seq can sequence any given RNA molecule from its three prime end regardless of its polyadenylation status without xxx need for PCR amplification or ligation of RNA adapters. We demonstrate that Nano3P seq captures a wide diversity of RNA biotypes providing quantitative estimates of RNA abundance and tail lengths in mRNA lncRNA sn/snoRNA scaRNA and rRNA molecules. We find that in addition to mRNA and lncRNA polyA tails can be identified in 16S mitochondrial rRNA in both mouse and zebrafish models. Moreover we show that mRNA tail lengths are dynamically regulated during vertebrate embryogenesis at an isoform specific level correlating with mRNA decay. Finally we identify non A bases within polyA tails of various lengths and reveal their distribution during vertebrate embryogenesis. Overall Nano3P seq is a simple and robust method for accurately estimating transcript levels tail lengths and tail composition heterogeneity in individual reads with minimal library preparation biases both in the coding and non coding transcriptome. | ENA FIRST PUBLIC:2022 10 10|ENA LAST UPDATE:2022 10 10 | Zebrafish Ribodepleted RNA 2hpf 4hpf 6hpf | Zebrafish Ribodepleted Rep1 | SAMEA110100411 | CENTER FOR GENOMIC REGULATION (CRG) | ENA FIRST PUBLIC:2022 10 10|ENA LAST UPDATE:2022 10 10|External Id:SAMEA110100411|INSDC center alias:CENTER FOR GENOMIC REGULATION CRG|INSDC center name:CENTER FOR GENOMIC REGULATION CRG|INSDC first public:2022 10 10T00:20:53Z|INSDC last update:2022 10 10T00:20:53Z|INSDC status:public|Submitter Id:Zebrafish Ribodepleted Rep1|common name:zebrafish|sample name:Zebrafish Ribodepleted Rep1 | MinION sequencing | ena EXPERIMENT TAB 13 06 2022 16:07:52:807 813 | cDNA786327 ZFRDR1 | 1 | RNA-Seq | TRANSCRIPTOMIC | other | SINGLE | OXFORD_NANOPORE | MinION | ERP138294 | MinION sequencing | ENA FIRST PUBLIC:2022 10 10|ENA LAST UPDATE:2022 10 10 | cDNA786327_ZFRDR1.tar.gz | nanopore | 1900613556.0 | 1660167.0 | ena RUN TAB 13 06 2022 16:07:52:807 814 | 0:1144.83 | A:473050820;C:438054520;G:425169743;T:564338473;N:0 | 1144 | 473050820 | 438054520 | 425169743 | 564338473 | 0 | ERX9385636 | ERS12199236 | ERA15547404 | CENTER FOR GENOMIC REGULATION (CRG)|European Nucleotide Archive | CENTER FOR GENOMIC REGULATION (CRG) | ont | ont | 3prime | poly_a | unknown | bulk | unknown | unknown | Spain | 2022-10-10 | Multi-stage | Embryo | Undetermined | Embryo Imprecise | ||||||||||||||||||||||||||||||
| 33866 | 33866 | SRR30779429 | SRX26181408 | SRS22725395 | SRP534298 | PRJNA1164307 | Time resolved single cell Multiomic zebrafish atlas | PRJNA1164307 | Other | During development dynamic interplay between transcription factors chromatin and genes termed gene regulatory network GRN shapes the cell fate determination along the developmental trajectory. Recent advances in joint measurement of chromatin accessibility and gene expression enabled the genome wide identification of regulatory relationships. Here we assess the dynamics of the gene regulatory network in zebrafish development using joint single cell ATAC and single cell RNA sequencing. We discovered some key regulatory modules that exhibit cell type and time dependent activity suggesting that the role of transcription factors vary over cell type and timepoints. With time resolved GRNs combined with linear modeling framework we performed a systematic in silico knock out simulation using CellOracle. This in silico knock out simulation revealed that the role of transcription factors is shared between mesodermal and neuro ectodermal lineages in the early timepoints but later commit significantly to either lineages. Together we provide a dataset and a framework to systematically dissect the role of transcription factors during the zebrafish embryonic development. | TDR124 | TDR124 24hpf EKW NA none 10xmultiome | strain:EKW|dev stage:30 somites 24 hpf|collection date:2023 08 17|geo loc name:USA: San Francisco|sex:N/A|tissue:organism|BioSampleModel:Model organism or animal | TDR124 24hpf RNA | TDR124 24hpf RNA EKW NA none 10xmultiome | TDR124 24hpf RNA EKW NA none 10xmultiome | 10x multiome nuc seq | RNA-Seq | TRANSCRIPTOMIC SINGLE CELL | cDNA | PAIRED | ILLUMINA | Illumina NovaSeq 6000 | SRP534298 | TDR124_24hpf_RNA_EKW_NA_none_10xmultiome_S2_L001_I1_001.fastq.gz TDR124_24hpf_RNA_EKW_NA_none_10xmultiome_S2_L001_I2_001.fastq.gz TDR124_24hpf_RNA_EKW_NA_none_10xmultiome_S2_L001_R1_001.fastq.gz TDR124_24hpf_RNA_EKW_NA_none_10xmultiome_S2_L001_R2_001.fastq.gz TDR124_24hpf_RNA_EKW_NA_none_10xmultiome_S2_L002_I1_001.fastq.gz TDR124_24hpf_RNA_EKW_NA_none_10xmultiome_S2_L002_I2_001.fastq.gz TDR124_24hpf_RNA_EKW_NA_none_10xmultiome_S2_L002_R1_001.fastq.gz TDR124_24hpf_RNA_EKW_NA_none_10xmultiome_S2_L002_R2_001.fastq.gz TDR124_24hpf_RNA_EKW_NA_none_10xmultiome_S2_L003_I1_001.fastq.gz TDR124_24hpf_RNA_EKW_NA_none_10xmultiome_S2_L003_I2_001.fastq.gz TDR124_24hpf_RNA_EKW_NA_none_10xmultiome_S2_L003_R1_001.fastq.gz TDR124_24hpf_RNA_EKW_NA_none_10xmultiome_S2_L003_R2_001.fastq.gz TDR124_24hpf_RNA_EKW_NA_none_10xmultiome_S2_L004_I1_001.fastq.gz TDR124_24hpf_RNA_EKW_NA_none_10xmultiome_S2_L004_I2_001.fastq.gz TDR124_24hpf_RNA_EKW_NA_none_10xmultiome_S2_L004_R1_001.fastq.gz TDR124_24hpf_RNA_EKW_NA_none_10xmultiome_S2_L004_R2_001.fastq.gz | fastq fastq fastq fastq fastq fastq fastq fastq fastq fastq fastq fastq fastq fastq fastq fastq | TDR124 24hpf RNA EKW NA none 10xmultiome S2 L001 I1 001.fastq.gz | SRX26181408 | SRA1977819 | Chan Zuckerberg Biohub San Francisco|Computational Biology | Chan Zuckerberg Biohub San Francisco | illumina | novaseq_era | unknown | cdna_unspecified | unknown | sc | single_cell_droplet | 10x | United States | 2024-09-23 | Multi-stage | Embryo | Undetermined | Embryo Imprecise |
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CREATE TABLE run_metadata("run.accession" VARCHAR, "experiment.accession" VARCHAR, "sample.accession" VARCHAR, "study.accession" VARCHAR, bioproject VARCHAR, "study.title" VARCHAR, "study.alias" VARCHAR, "study.type" VARCHAR, "study.abstract" VARCHAR, "study.attributes" VARCHAR, "study.PMIDs" VARCHAR, "sample.description" VARCHAR, "sample.title" VARCHAR, "sample.alias" VARCHAR, "sample.centername" VARCHAR, "sample.attributes" VARCHAR, "GEOsample.title" VARCHAR, "GEOsample.dataprocessing" VARCHAR, "GEOsample.source" VARCHAR, "GEOsample.treatmentprotocol" VARCHAR, "GEOsample.extractprotocol" VARCHAR, "GEOsample.growthprotocol" VARCHAR, "GEOsample.characteristics" VARCHAR, "GEOsample.accession" VARCHAR, "experiment.title" VARCHAR, "experiment.alias" VARCHAR, "experiment.library_name" VARCHAR, "experiment.design_description" VARCHAR, "experiment.library_construction_protocol" VARCHAR, "experiment.attributes" VARCHAR, "experiment.library_strategy" VARCHAR, "experiment.library_source" VARCHAR, "experiment.library_selection" VARCHAR, "experiment.library_layout" VARCHAR, "experiment.platform" VARCHAR, "experiment.instrument_model" VARCHAR, "experiment.spot_descriptor" VARCHAR, "experiment.study_ref" VARCHAR, "run.title" VARCHAR, "run.attributes" VARCHAR, "run.filename" VARCHAR, "run.semantic_name" VARCHAR, "run.total_bases" DOUBLE, "run.total_spots" DOUBLE, "run.alias" VARCHAR, "run.read_lengths" VARCHAR, "run.base_counts" VARCHAR, "run.r1_length" BIGINT, "run.r2_length" BIGINT, "run.r3_length" BIGINT, "run.r4_length" BIGINT, "run.Acount" BIGINT, "run.Ccount" BIGINT, "run.Gcount" BIGINT, "run.Tcount" BIGINT, "run.Ncount" BIGINT, "run.experiment" VARCHAR, "run.pool_member" VARCHAR, "submission.accession" VARCHAR, "submission.srasource" VARCHAR, "submission.bioprojectsource" VARCHAR, "seqdetective.n_mates" BIGINT, "seqdetective.mapping_rate.mate1" DOUBLE, "seqdetective.mapping_rate.mate2" DOUBLE, "seqdetective.nofeature_rate.mate1" DOUBLE, "seqdetective.nofeature_rate.mate2" DOUBLE, "seqdetective.sparsity.mate1" DOUBLE, "seqdetective.sparsity.mate2" DOUBLE, "seqdetective.pos_strand_rate.mate1" DOUBLE, "seqdetective.pos_strand_rate.mate2" DOUBLE, "seqdetective.readlen.mate1" BIGINT, "seqdetective.readlen.mate2" BIGINT, "seqdetective.judgement.mate1" VARCHAR, "seqdetective.judgement.mate2" VARCHAR, "seqdetective.judgement.reason" VARCHAR, platform_family VARCHAR, instrument_generation VARCHAR, read_bias VARCHAR, selection_class VARCHAR, prep_kit VARCHAR, sc_or_bulk VARCHAR, tech_class VARCHAR, technology VARCHAR, tech_variant VARCHAR, "submission.bioprojectsource.country" VARCHAR, earliest_date DATE, devstage_curation VARCHAR, devstage_curation_coarse VARCHAR, tissue_curation VARCHAR, tissue_curation_coarse VARCHAR);;
CREATE INDEX idx_run_bioproject ON run_metadata(bioproject);;
CREATE INDEX idx_run_run_accession ON run_metadata("run.accession");;