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Merge pull request #1197 from maxulysse/tower_yml
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Greatly improve tower.yml file
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maxulysse authored Aug 30, 2023
2 parents 575c707 + 2e4caae commit ce149be
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1 change: 1 addition & 0 deletions CHANGELOG.md
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Expand Up @@ -47,6 +47,7 @@ and this project adheres to [Semantic Versioning](https://semver.org/spec/v2.0.0
- [#1183](https://github.com/nf-core/sarek/pull/1183) - Add docs for concatentated germline variants
- [#1184](https://github.com/nf-core/sarek/pull/1184) - Fix issue with duplicated variants in VCF from Sentieon-based joint-germline variant-calling with VQSR. (Corresponding to [#966](https://github.com/nf-core/sarek/issues/966) for GATK.)
- [#1192](https://github.com/nf-core/sarek/pull/1192) - Add `ASCATprofile.png` to ASCAT output docs
- [#1197](https://github.com/nf-core/sarek/pull/1197) - Improve `tower.yml` file to display reports in `Tower` ([#1190](https://github.com/nf-core/sarek/issues/1190))

### Dependencies

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58 changes: 56 additions & 2 deletions tower.yml
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reports:
multiqc_report.html:
display: "MultiQC HTML report"
samplesheet.csv:
display: "Auto-created samplesheet with collated metadata and FASTQ paths"
"**/umi/*_umi_histogram.txt":
display: "All UMI histograms"
"**/reports/fastp/*/*_fastp.html":
display: "FASTP report"
"**/reports/mosdepth/*/*.mosdepth.summary.txt":
display: "All samples summary of mean depths per chromosome and within specified regions per chromosome"
"**/csv/*.csv":
display: "All CSV files to restart nf-core/sarek at a different step"
"**/variantcalling/ascat/*/*.tumour.ASPCF.png":
display: "ASCAT: All allele-specific copy number segmentation images"
"**/variantcalling/ascat/*/*.before_correction_Tumour.*.png":
display: "ASCAT: All samples logR and BAF values"
"**/variantcalling/ascat/*/*.after_correction_GC_Tumour.*.png":
display: "ASCAT: All samples GC and RT corrected logR and BAF values"
"**/variantcalling/ascat/*/*.tumour.sunrise.png":
display: "ASCAT: Range of ploidy and tumor percentage values"
"**/variantcalling/ascat/*/*.metrics.txt":
display: "ASCAT: Multiple metrics information"
"**/variantcalling/ascat/*/*.cnvs.txt":
display: "ASCAT: CNVS information"
"**/variantcalling/ascat/*/*.purityploidy.txt":
display: "ASCAT: Purity and ploidy information"
"**/variantcalling/ascat/*/*.segments.txt":
display: "ASCAT: copy number segments information"
"**/variantcalling/ascat/*/*_tumourBAF.txt":
display: "ASCAT: beta allele frequencies"
"**/variantcalling/ascat/*/*.tumour_*LogR.txt":
display: "ASCAT: total copy number on a logarithmic scale"
"**/variantcalling/cnvkit/*/*-diagram.pdf":
display: "CNVKIT: Copy numbers or segments on chromosomes"
"**/variantcalling/cnvkit/**-scatter.png":
display: "CNVKIT: Bin-level log2 coverages and segmentation calls"
"**/variantcalling/controlfreec/*/config.txt":
display: "Control-FREEC: Configuration file used to run Control-FREEC"
"**/variantcalling/controlfreec/*/*_BAF.png":
display: "Control-FREEC: BAF plot"
"**/variantcalling/controlfreec/*/*_ratio.log2.png":
display: "Control-FREEC: log2 ratio plot"
"**/variantcalling/controlfreec/*/*_ratio.png":
display: "Control-FREEC: ratio plot"
"**/variantcalling/controlfreec/*/*.circos.txt":
display: "Control-FREEC: translated output to the Circos format"
"**/variantcalling/controlfreec/*/*.p.value.txt":
display: "Control-FREEC: CNV file containing p_values for each call"
"**/variantcalling/controlfreec/*/*_BAF.txt":
display: "Control-FREEC: file with beta allele frequencies for each possibly heterozygous SNP position"
"**/variantcalling/controlfreec/*/*_info.txt":
display: "Control-FREEC: parsable file with information about FREEC run"
"**/reports/bcftools/*.bcftools_stats.txt":
display: "All samples raw statistics"
"**/reports/SnpEff/*/*/*_snpEff.html":
display: "Statistics and plots for the SnpEff run"
"**/reports/SnpEff/*/*/*_snpEff.genes.txt":
display: "TXT (tab separated) summary counts for variants affecting each transcript and gene"
"**/reports/EnsemblVEP/*/*/*_VEP.summary.html":
display: "Summary of the VEP run"

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