README.md

June 26, 2025 ยท View on GitHub

Analysis Modules

This directory contains various analysis modules in the OpenPedCan project. See the README of an individual analysis modules for more information about that module.

Modules at a glance

The table below is intended to help project organizers quickly get an idea of what files (and therefore types of data) are consumed by each analysis module, what the module does, and what output files it produces that can be consumed by other analysis modules. This is in service of documenting interdependent analyses. Note that nearly all modules use the harmonized clinical data file (histologies.tsv) even when it is not explicitly included in the table below.

ModuleInput FilesBrief DescriptionProduces files for data release?Output Files Consumed by Other AnalysesAdapted for OPC?Run PlatformAction Plan
chromosomal-instabilityhistologies.tsv sv-manta.tsv.gz cnv-cnvkit.seg.gzEvaluates chromosomal instability by calculating chromosomal breakpoint densities and by creating circular plot visualsNobreakpoint-data/union_of_breaks_densities.tsvNoN/AWill Adapt for OT
chromothripsissv-manta.tsv.gz cnv-consensus.seg.gz independent-specimens.wgs.primary-plus.tsvPerforms chromothripsis analysisNoN/ANoN/AN/A
cnv-chrom-plotcnv-consensus-gistic.zip cnv-consensus.segPlots genome wide visualizations relating to copy number resultsNoN/ANoN/AN/A
cnv-frequencies (MTP-specific)histologies.tsv consensus_wgs_plus_cnvkit_wxs.tsv.gz independent-specimens.wgswxspanel.primary.eachcohort.tsv independent-specimens.wgswxspanel.relapse.eachcohort.tsv independent-specimens.wgswxspanel.primary.tsv independent-specimens.wgswxspanel.relapse.tsvAnnotates CNV table with frequenciesNoresults/gene-level-cnv-consensus-annotated-mut-freq.jsonl.gz results/gene-level-cnv-consensus-annotated-mut-freq.tsv.gzYesGitHubN/A
collapse-rnaseq (ported to CAVATICA)gene-expression-rsem-tpm.rds gencode.v39.primary_assembly.annotation.gtf.gzCollapses RSEM count and TPM matrices such that gene symbols are de-duplicated.Yesresults/gene-expression-rsem-fpkm-collapsed.rds included in data download; too large for tracking via GitHubYesCAVATICAN/A
copy_number_consensus_callcnv-cnvkit.seg.gz cnv-controlfreec.tsv.gz sv-manta.tsv.gzProduces consensus copy number calls and a set of excluded regions where CNV calls are not madeYesresults/cnv_consensus.tsv 'results/uncalled_samples.tsv' results/cnv-consensus.seg.gz included in data download ref/cnv_excluded_regions.bed ref/cnv_callable.bedYesCAVATICAN/A
create-subset-filesAll filesThis module contains the code to create the subset files used in GitHub ActionsNoAll subset files for continuous integrationNoN/AWill set up for OT ticket in
data-pre-release-qchistologies-base.tsv gene-counts-rsem-expected_count-collapsed.rds gene-expression-rsem-tpm-collapased.rds tcga-gene-counts-rsem-expected_count-collapsed.rds tcga-gene-expression-rsem-tpm-collapsed.rds cnv-cnvkit.seg.gz cnvkit_with_status.tsv consensus_wgs_plus_cnvkit_wxs_autosomes.tsv.gz consensus_wgs_plus_cnvkit_wxs_x_and_y.tsv.gz snv-mutation-tmb-all.tsv fusion_summary_embryonal_foi.tsv fusion_summary_ependymoma_foi.tsv fusion_summary_lgg_hgg_foi.tsv fusion_summary_ewings_foi.tsv biospecimen_id_to_bed_map.txtPerforms QC on data pre-release files with requirements which should pass before hand off between BIXU Engineering team to the OpenPedCan teamYes'data-pre-release-qc.nb.html'NoN/AN/A
efo-mondo-mapping (MTP-specific)histologies.tsv efo-mondo-map.tsvThis module contains a file with EFO, MONDO, and NCIT codes for all cancer_group found in histologies.tsv and runs a script to qc in case any cancer_group is missedYesefo-mondo-mapping.tsvYesN/AYes
filter-mtp-tables (MTP-specific)gencode.v39.primary_assembly.annotation.gtf.gz PMTL_v1.1.tsv histologies.tsv gene-level-snv-consensus-annotated-mut-freq.tsv.gz snv-consensus-plus-hotspots.maf.tsv.gz variant-level-snv-consensus-annotated-mut-freq.tsv.gz gene-level-cnv-consensus-annotated-mut-freq.tsv.gz consensus_wgs_plus_cnvkit_wxs.tsv.gz putative-oncogene-fusion-freq.tsv.gz fusion-putative-oncogenic.tsv putative-oncogene-fused-gene-freq.tsv.gz long_n_tpm_mean_sd_quantile_gene_wise_zscore.tsv.gz long_n_tpm_mean_sd_quantile_group_wise_zscore.tsv.gzRemoves Ensembl (ESNG) gene identifier in the OpenPedCan mutation frequency tables, including SNV, CNV, fusion, and TPM expression tables that are not in GENCODE v39 and Ensembl package 104.NoAll files from module results directoryYesN/AYes
focal-cn-file-preparationcnv-cnvkit.seg.gz cnv-controlfreec.tsv.gz gene-expression-rsem-tpm-collapsed.rds cnv-consensus.seg.gzMaps from copy number variant caller segments to gene identifiers; will be updated to take into account changes that affect entire cytobands, chromosome armsYescnvkit_annotated_cn_wxs_autosomes.tsv.gz cnvkit_annotated_cn_wxs_x_and_y.tsv.gz consensus_seg_annotated_cn_autosomes.tsv.gz consensus_seg_annotated_cn_x_and_y.tsv.gz consensus_seg_most_focal_fn_status.tsv.gz consensus_seg_recurrent_focal_cn_units.tsv consensus_seg_with_ucsc_cytoband_status.tsv.gz consensus_wgs_plus_cnvkit_wxs_autosomes.tsv.gzincluded in data download consensus_wgs_plus_cnvkit_wxs_x_and_y.tsv.gz` included in data downloadYesCAVATICAN/A
fusion_filteringfusion-arriba.tsv.gz fusion-starfusion.tsv.gz independent-specimens.rnaseq.primary.tsv independent-specimens.rnaseq.relapse.tsvStandardizes, filters, and prioritizes fusion callsYesresults/fusion-putative-oncogenic.tsv included in data download results/fusion-recurrent-fusion-bycancergroup.tsv results/fusion-recurrent-fusion-bysample.tsv results/fusion-recurrently-fused-genes-bycancergroup.tsv results/fusion-recurrently-fused-genes-bysample.tsvYesGitHubN/A
fusion-frequencies (MTP-specific)histologies.tsv fusion-putative-oncogenic.tsv fusion-dgd.tsv.gz independent-specimens.rnaseqpanel.primary.tsv independent-specimens.rnaseqpanel.relapse.tsv independent-specimens.rnaseqpanel.primary.eachcohort.tsv independent-specimens.rnaseqpanel.relapse.eachcohort.tsvGathers counts and frequencies for fusion per cancer_group and cohortNoresults/putative-oncogene-fused-gene-freq.jsonl.gz results/putative-oncogene-fused-gene-freq.tsv.gz results/putative-oncogene-fusion-freq.jsonl.gz results/putative-oncogene-fusion-freq.tsv.gzYesGitHubN/A
fusion-summaryhistologies.tsv fusion-putative-oncogenic.tsv fusion-arriba.tsv.gz fusion-starfusion.tsv.gzGenerates summary matrices of fusions in preparation for molecular subtypingYesresults/fusion_summary_embryonal_foi.tsv results/fusion_summary_ependymoma_foi.tsv results/fusion_summary_ewings_foi.tsvYesGitHubN/A
gene_match (MTP-specific)GTF file sources: gencode v28 gencode v38 open_ped_can_v7_ensg-hugo-rmtl-mapping.tsvReads GTF file and formats attributes to extract gene symbol with gene ensembl ID.Yesensg-hugo-pmtl-mapping.tsvYesGitHubN/A
gene-set-enrichment-analysisgene-expression-rsem-tpm-collapsed.rds histologies.tsvPerforms gene set enrichment analysis by RNA libraryNoresults/gsva_scores.tsv combined file for all RNA library typesYesGitHubMove to CAVATICA
immune-deconvgene-expression-rsem-tpm-collapsed.rds data/histologies.tsvPerforms immune cell deconvolution using Xcell and quantiseqNoxcell_output.rds quantiseq_output.rdsNoN/AN/A
independent-sampleshistologies.tsvGenerates independent specimen lists by experimental strategy and/or cohortYesresults/independent-specimens.wgswxspanel.primary.tsv included in data download results/independent-specimens.wgswxspanel.relapse.tsv included in data download results/independent-specimens.wgswxspanel.primary.eachcohort.tsv included in data download results/independent-specimens.wgswxspanel.relapse.eachcohort.tsv included in data download results/independent-specimens.wgswxspanel.primary.prefer.wxs.tsv included in data download results/independent-specimens.wgswxspanel.relapse.prefer.wxs.tsv included in data download results/independent-specimens.wgswxspanel.primary.eachcohort.prefer.wxs.tsv included in data download results/independent-specimens.wgswxspanel.relapse.eachcohort.prefer.wxs.tsv included in data download results/independent-specimens.rnaseq.primary.tsv included in data download results/independent-specimens.rnaseq.relapse.tsv included in data download results/independent-specimens.rnaseq.primary.eachcohort.tsv included in data download results/independent-specimens.rnaseq.relapse.eachcohort.tsv included in data downloadYesGitHubN/A
interaction-plotsindependent-specimens.wgs.primary-plus.tsv snv-consensus-mutation.maf.tsv.gzCreates interaction plots for mutation mutual exclusivity/co-occurrenceNoN/ANoN/AN/A
long-format-table-utils (MTP-specific)ensg-hugo-rmtl-mapping.tsv analyses/fusion_filtering/references/genelistreference.txt efo-mondo-map.tsv uberon-map-gtex-group.tsv uberon-map-gtex-subgroup.tsvFunctions and scripts for handling long-format tablesNoannotator/annotation-data/ensg-gene-full-name-refseq-protein.tsv annotator/annotation-data/oncokb-cancer-gene-list.tsvYesGitHubN/A
methylation-preprocessing (ported to CAVATICA)TARGET_Normal_MethylationArray_20160812.sdrf.txt TARGET_NBL_MethylationArray_20160812.sdrf.1.txt TARGET_NBL_MethylationArray_20160812.sdrf.2.txt TARGET_CCSK_MethylationArray_20160819.sdrf.txt TARGET_OS_MethylationArray_20161103.sdrf.txt TARGET_WT_MethylationArray_20160831.sdrf.txt TARGET_AML_MethylationArray_20160812_450k.sdrf.1.txt TARGET_AML_MethylationArray_20160812_450k.sdrf.2.txt TARGET_AML_MethylationArray_20160812_27k.sdrf.1.txt TARGET_AML_MethylationArray_20160812_27k.sdrf.2.txt TARGET_AML_MethylationArray_20160812_27k.sdrf.3.txt manifest_methylation_CBTN_20220410.1.csv manifest_methylation_CBTN_20220410.2.csv manifest_methylation_CBTN_20220410.3.csv manifest_methylation_CBTN_20220410.4.csvPreprocesses probe hybridization intensity values of selected methylated and unmethylated cytosine (CpG) loci into usable methylation measurements (m-values, beta values, and cnvs).NoN/AYesCavaticaN/A
methylation-summary (ported to CAVATICA)infinium.gencode.v39.probe.annotations.tsv.gz independent-specimens.rnaseqpanel.eachchort.tsv independent-specimens.methyl.eachcohort.tsv gene-expression-rsem-tpm-collapsed.rds rna-isoform-expression-rsem-tpm.rds methyl-beta-values.rds efo-mondo-map.tsv histlogies.tsvSummarizes preprocessed Illumina Infinium Human Methylation array measurements produced by methylation preprocessing using Illumina infinium methylation array CpG probe coordinates.NoN/ANoawsN/A
molecular-subtyping-ATRThistologies-base.tsvMolecular subtyping of ATRTsNoNAGitHubN/A
molecular-subtyping-CRANIOhistologies-base.tsv snv-consensus-plus-hotspots.maf.tsv.gzMolecular subtyping of craniopharyngiomasNoresults/CRANIO_molecular_subtype.tsvNoN/APrepare for scaling
molecular-subtyping-EPNhistologies-base.tsv gene-expression-rsem-tpm-collapsed.rds analyses/chromosomal-instability/breakpoint-data/union_of_breaks_densities.tsv analyses/fusion-summary/results/fusion_summary_ependymoma_foi.tsv analyses/gene-set-enrichment-analysis/results/gsva_scores.tsvmolecular subtyping of ependymomasNoresults/EPN_all_data_withsubgroup.tsvNoN/AWill Adapt for OT
molecular-subtyping-EWShistologies-base.tsv analyses/fusion-summary/results/fusion_summary_ewings_foi.tsvReclassifies tumors based on the presence of defining fusions for Ewing SarcomasNoresults/EWS_samples.tsvNoN/AWill Adapt for OT
molecular-subtyping-HGGhistologies-base.tsv snv-consensus-plus-hotspots.maf.tsv.gz consensus_wgs_plus_cnvkit_wxs.tsv.gz fusion-putative-oncogenic.tsv cnv-consensus-gistic.zip gene-expression-rsem-tpm-collapsed.rds tp53_altered_status.tsvMolecular subtyping of high-grade gliomasNoresults/HGG_molecular_subtype.tsvYesGitHubN/A
molecular-subtyping-LGAThistologies-base.tsv snv-consensus-plus-hotspots.maf.tsv.gz fusion-putative-oncogenic.tsv analyses/fusion_filtering/results/fusion-recurrently-fused-genes-bysample.tsvMolecular subtyping of low-grade gliomasNoresults/lgat_subtyping.tsvYesGitHubN/A
molecular-subtyping-MBhistologies-base.tsv gene-expression-rsem-tpm-collapsed.rdsMolecular classification of medulloblastomasNoresults/MB_molecular_subtype.tsvYesGitHubN/A
molecular-subtyping-chordomaanalyses/focal-cn-file-preparation/results/consensus_seg_annotated_cn_autosomes.tsv.gz gene-expression-rsem-fpkm-collapsed.stranded.rdsidentifies poorly-differentiated chordomasNoN/ANoN/AWill Adapt for OT
molecular-subtyping-embryonalhistologies-base.tsv analyses/fusion-summary/fusion_summary_embryonal_foi.tsv sv-manta.tsv.gz consensus_wgs_plus_cnvkit_wxs.tsv.gz analyses/focal-cn-file-preparation/cnvkit_annotated_cn_x\_and_y.tsv.gz analyses/focal-cn-file-preparation/controlfreec_annotated_cn_x\_and_y.tsv.gz gene-expression-rsem-tpm-collapsed.rdsMolecular subtyping of non-medulloblastoma, non-ATRT embryonal tumorsNoresults/embryonal_tumor_molecular_subtypes.tsvNoN/AWill Adapt for OT
molecular-subtyping-integratehistologies-base.tsv results/compiled_molecular_subtypes_with_clinical_pathology_feedback.tsvAdds molecular subtype information to the base histology fileNoresults/histologies.tsvYesGitHubN/A
molecular-subtyping-NBLhistologies-base.tsv consensus_wgs_plus_cnvkit_wxs.tsv.gz cnv-cnvkit.seg.gz cnv-controlfreec.tsv.gz gene-expression-rsem-tpm-collapsed.rds analyses/molecular-subtyping-NBL/input/gmkf_patient_clinical_mycn_status.tsv analyses/molecular-subtyping-NBL/input/target_patient_clinical_mycn_status.tsvMolecular subtyping of neuroblastomasNoresults/NBL_MYCN_Subtype.tsv results/Alteration_Table.tsv results/Subtypes_Based_On_Cutoff.tsv results/QC_table.tsvYesEC2N/A
molecular-subtyping-neurocytomahistologies-base.tsvMolecular subtyping of neurocytomasNoresults/neurocytoma_subtyping.tsvNoN/AWill Adapt for OT
molecular-subtyping-pathologyanalyses/molecular-subtyping-CRANIO/results/CRANIO_molecular_subtype.tsv analyses/molecular-subtyping-EPN/results/CRANIO_molecular_subtype.tsv analyses/molecular-subtyping-MB/results/MB_molecular_subtype.tsv analyses/molecular-subtyping-neurocytoma/results/neurocytoma_subtyping.tsv analyses/molecular-subtyping-EWS/results/EWS_samples.tsv analyses/molecular-subtyping-HGG/results/HGG_molecular_subtype.tsv analyses/molecular-subtyping-LGAT/results/lgat_subtyping.tsv analyses/molecular-subtyping-embryonal/results/embryonal_tumor_molecular_subtypes.tsvCompiles output from other molecular subtyping modules and incorporate pathology feedbackNochoroid_plexus_papilloma_subtypes.tsv cns-lymphoma-subtypes.tsv compiled_molecular_subtypes.tsv compiled_molecular_subtypes_and_report_info.tsv compiled_molecular_subtypes_with_clinical_feedback_and_report_info.tsv compiled_molecular_subtypes_with_clinical_pathology_feedback_and_report_info.tsv cranio_adam_subtypes.tsv glialneuronal_tumor_subtypes.tsv juvenile-xanthogranuloma-subtypes.tsv lgat-pathology-free-text-subtypes.tsv meningioma_subtypes.tsvYesGitHubN/A
molecular-subtyping-PBhistologies-base.tsvMolecular subtyping of pineoblastomasNoresults/pineo-molecular-subtypes.tsvYesGitHubN/A
mtp-annotations (MTP-specific)scratch/mtp-json/targets/ scratch/mtp-json/diseases/Transforms the OpenTargets Platform Target (core annotations for targets) and Disease/Phenotype (core annotations for diseases and phenotypes) tables into mapping files utilized in filtering MTP designated tables and OPC data release files for plotting API developmentNoN/AlocalN/AN/A
mtp-tables-qc-checks (MTP-specific)gene-level-cnv-consensus-annotated-mut-freq.tsv.gz gene-level-snv-consensus-annotated-mut-freq.tsv.gz gene-variant-snv-consensus-annotated-mut-freq.tsv.gz putative-oncogene-gused-gene-freq.tsv.gz putative-oncogene-fusion-freq.tsv.gz long_n_tpm_mean_sd_quantitle_gene_wise_zscore.tsv.gz long_n_tpm_mean_sd_quatile_group_wise_zscore.tsv.gzPerforms summary and QC checks comparing the current and the previous OPC mutation frequencies tableNoN/ANoN/AN/A
mutational-signaturessnv-consensus-plus-hotspots.maf.tsv.gzPerforms COSMIC and Alexandrov et al. mutational signature analysis using the consensus SNV dataNoN/ANoN/AN/A
oncoprint-landscapesnv-consensus-plus-hotspots.maf.tsv.gz fusion-putative-oncogenic.tsv analyses/focal-cn-file-preparation/results/controlfreec_annotated_cn_autosomes.tsv.gz independent-specimens.\*Combines mutation, copy number, and fusion data into an OncoPrint plotNoN/ANoN/AN/A
pedcbio-cnv-prepareconsensus_wgs_plus_cnvkit_wxs_autosomes.tsv.gz consensus_wgs_plus_cnvkit_wxs_x\_and_y.tsv.gzGenerates annotated CNV files that are similar to seg files for PedCBio uploads to include all samples with neutral CNV callsYesUpload to PedCBio S3 bucket for ingestionGitHubN/AN/A
pedcbio-sample-namehistologies.tsv input\cbtn_cbio_sample.csv input\dgd_cbio_sample.csv input\oligo_nation_cbio_sample.csv input\x01_fy16_nbl_maris_cbio_sample.csvFormats sample names for pedcbio when multiple DNA or RNA specimens are associated with the same sampleYesUpload to PedCBio S3 bucket for ingestionGitHubN/AN/A
pedot-table-column-display-order-nameanalyses/snv-frequencies/results/gene-level-snv-consensus-annotated-mut-freq.tsv analyses/snv-frequencies/results/variant-level-snv-consensus-annotated-mut-freq.tsv.gz analyses/cnv-frequencies/results/gene-level-cnv-consensus-annotated-mut-freq.tsv.gz analyses/fusion-frequencies/results/putative-oncogene-fused-gene-freq.tsv.gz analyses/fusion-frequencies/results/putative-oncogene-fusion-freq.tsv.gz analyses/rna-seq-expression-summary-stats/results/long_n\_tpm_mean_sd_quantile_gene_wise_zscore.tsv.gz analyses/rna-seq-expression-summary-stats/results/long_n\_tpm_mean_sd_quantile_group_wise_zscore.tsv.gzGenerates and validates an Excel spreadsheet for Pediatric Open Targets PedOT website table display orders and namesNoUpload to FNL BOXYesGitHubN/A
rnaseq-batch-correctgene-counts-rsem-expected_count-collapsed.rds histologies.tsv hk_genes_normals.rds [positive_control_genes].rdsPerforms RUVseq-DESeq2 batch-corrected DGE analysisYesN/AYesGithubN/A
rna-seq-expression-summary-stats (MTP-specific)gene-expression-rsem-tpm-collapsed.rds histologies.tsvCalculates TPM summary statistics within each cancer group and cohort. #51.NoUpload to FNL BoxYesGitHubN/A
run-gistichistologies.tsv cnv-consensus.seg.gzRuns GISTIC 2.0 on SEG filesYescnv-consensus-gistic.zip included in data downloadYesGitHubMove to CAVATICA
snv-frequencies (MTP-specific)histologies.tsv snv-consensus-plus-hotspots.maf.tsv.gz snv-dgd.maf.tsv.gz independent-specimens.wgswxspanel.primary.eachcohort.prefer.wxs.tsv independent-specimens.wgswxspanel.relapse.eachcohort.prefer.wxs.tsv independent-specimens.wgswxspanel.primary.prefer.wxs.tsv independent-specimens.wgswxspanel.relapse.prefer.wxs.tsvAnnotates SNV table with mutation frequenciesNoresults/gene-level-snv-consensus-annotated-mut-freq.jsonl.gz results/gene-level-snv-consensus-annotated-mut-freq.tsv.gz variant-level-snv-consensus-annotated-mut-freq.jsonl.gz variant-level-snv-consensus-annotated-mut-freq.tsv.gzYesGitHubN/A
survival-analysisTBDContains survival analysis templatesNoN/ANoN/AN/A
telomerase-activity-predictiongene-expression-rsem-tpm-collapsed.rds gene-counts-rsem-expected_count-collapsed.rdsQuantifies telomerase activity using RNA-SeqNoresults/TelomeraseScores_PTBAPolya_counts results/TelomeraseScores_PTBAPolya_FPKM.txt results/TelomeraseScores_PTBAStranded_counts.txt results/TelomeraseScores_PTBAStranded_FPKM.txtNoN/AN/A
tmb-calculationgencode.v27.primary_assembly.annotation.bed intersect_strelka_mutect2_vardict_WGS.bed snv-consensus-plus-hotspots.maf.tsv.gz biospecimen_id_to_bed_map.tsv histologies-base.tsv hg38_strelka.bed wgs_canonical_calling_regions.hg38.bed gencode.v39.primary_assembly.annotation.gtf.gzCalculates TMB using consensus SNV calls for tumors with paired T/N variant calls onlyYessnv-mutation-tmb-all.tsv snv-mutation-tmb-coding.tsvYesGitHubN/A
tp53_nf1_scoresnv-consensus-plus-hotspots.maf.tsv gene-expression-rsem-tpm-collapsed.rds consensus_wgs_plus_cnvkit_wxs.tsv.gzApplies TP53 inactivation classifier to RNA-Seq dataNoTP53_NF1_snv_alteration.tsv gene-expression-rsem-tpm-collapsed_classifier_scores.tsv loss_overlap_domains_tp53.tsv poly-A_TP53.png stranded_TP53.png sv_overlap_tp53.tsv tp53_altered_status.tsvYesGitHubN/A
transcriptomic-dimension-reductiongene-expression-rsem-tpm.rds gene-expression-kallisto.rdsPerforms dimension reduction and visualization of RNA-seq dataNoN/ANoN/AN/A
tumor-gtex-plots (MTP-specific)gene-expression-rsem-tpm-collapsed.rds histologies.tsvTumor vs normal (GTEx) and tumor only expression plotsNoresults/pan_cancer_plots_cancer_group_level.{tsv, jsonl.gz} results/pan_cancer_plots_cohort_cancer_group_level.{tsv, jsonl.gz} results/tumor_normal_gtex_plots_cancer_group_level.{tsv, jsonl.gz} results/tumor_normal_gtex_plots_cohort_cancer_group_level.{tsv, jsonl.gz} results/metadata.tsv plots/\*.pngYesGitHubN/A
tumor-normal-differential-expression (MTP-specific)histologies.tsv gene-counts-rsem-expected_count-collapsed.rds independent-specimens.rnaseq.primary.tsv independent-specimens.rnaseq.primary.eachcohort.tsv gene-expression-rsem-tpm-collapsed.rds ensg-hugo-pmtl-mapping.tsv efo-mondo-map.tsv uberon-map-gtex-subgroup.tsvPerforms differential expression analysis for all combinations of GTEx subgroup normal and cancer histology type tumor.NoN/A