run_metadata: 51964
This data as json
| 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 |
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| 51964 | SRR8928875 | SRX5709832 | SRS4649003 | SRP193005 | PRJNA533623 | MITF low zebrafish melanomas reveal cells with no MITF activity at the site of residual disease | GSE130037 | Transcriptome Analysis | The MITF low melanoma transcriptional signature is predictive of poor outcome for patients but little is known about its biological signature. We used genetic models of zebrafish with low expression of mitfa MITF low to study this biological subtype. We performed whole bulk RNA seq to classify zebrafish MITF low melanoma that cluster mainly by their directionality of growth and assess their resemblance to patients' MITF low subgroups. Furthermore using genetic inhibition of MITF activity we discover minimal residual disease at the site of regression and using single cell and low input RNA seq we characterise these MITF independent cells and show that they pre exist in the primary tumour. Overall design: We performed bulk RNAseq experiment of zebrafish primary melanomas to compare different phenotypes based on directionality of growth or original mutations. Further we performed single cell RNAseq of primary and regressed melanoma. | pubmed:31582381 | GC056865 GCGTAGTA TCGACTAG control psbulk | GSM3730586 | source name:mitfa:GFP cells from control|genotype:mitfavc7|tissue:GFP+ cells from control | GC056865 GCGTAGTA TCGACTAG control psbulk | Sequence quality was checked using FastQC version 0.11.4. Raw reads were trimmed using Cutadapt to remove Smart Seq2 adaptor sequences. The trimmed reads were mapped using STAR to the reference genome version GRCz11 Ensembl V92 20178 including coding sequences for EGFP and hsBRAFV600E and point mutations in p53 and mitfa. Aligned reads were quantified using Salmon in the alignment based mode. Illumina software used for basecalling. Sequence quality was checked using FastQC version 0.11.3 Reads were aligned to the zebrafish genome GRCz11 using STAR STAR 2.5.1b with the default parameters or using Salmon in the alignment based mode The quality of the resulting alignment to the transcriptome Ensembl annotation version GRCz11 has been checked using RNASeqQC v1.1.8.1 Raw counts of reads covering the transcriptome Ensembl annotation version GRCz11 was obtained using htseq count 0.6.1 with the “ s reverse” option. Genome build: Zebrafish GRCz11 Supplementary files format and content: tab delimited filed of raw counts at gene level for each sample | mitfa:GFP cells from control | FACS sorting of 50 GFP+ living cells from control SMARTseq2 Picelli et al 2014 polyA selection cDNA TruSeq or Nextera XT RNA Seq Paired end reads | genotype:mitfavc7|tissue:GFP+ cells from control | GSM3730586 | GSM3730586: GC056865 GCGTAGTA TCGACTAG control psbulk; Danio rerio; RNA Seq | GSM3730586 | 1 | FACS sorting of 50 GFP+ living cells from control SMARTseq2 Picelli et al 2014 polyA selection cDNA TruSeq or Nextera XT RNA Seq Paired end reads | GEO Accession:GSM3730586 | RNA-Seq | TRANSCRIPTOMIC | cDNA | PAIRED | ILLUMINA | Illumina HiSeq 2500 | SRP193005 | GC056865_GCGTAGTA-TCGACTAG.R1.fastq.gz GC056865_GCGTAGTA-TCGACTAG.R2.fastq.gz | fastq fastq | 397190556.0 | 1576153.0 | GSM3730586 r1 | 0:126 1:126 | A:108614389;C:88489174;G:87744396;T:112305346;N:37251 | 126 | 126 | 108614389 | 88489174 | 87744396 | 112305346 | 37251 | SRX5709832 | SRS4649003 | SRA876955 | GEO | Prof. Patton lab, MRC Institute of Genetics and Molecular Medicine, MRC Human Genetics Unit & Cancer Research UK EC | 2 | 0.91036 | 0.90994 | 0.14864 | 0.15033 | 0.82856 | 0.82775 | 0.55841 | 0.55225 | 126 | 126 | B | B | biological fallback assumption | illumina | hiseq_era | unknown | poly_a | nextera | sc | single_cell_plate | smartseq | United Kingdom | 2019-04-18 | Undetermined | Undetermined | Undetermined | Undetermined |