-
Notifications
You must be signed in to change notification settings - Fork 420
Commit
This commit does not belong to any branch on this repository, and may belong to a fork outside of the repository.
Merge pull request #1197 from maxulysse/tower_yml
Greatly improve tower.yml file
- Loading branch information
Showing
2 changed files
with
57 additions
and
2 deletions.
There are no files selected for viewing
This file contains bidirectional Unicode text that may be interpreted or compiled differently than what appears below. To review, open the file in an editor that reveals hidden Unicode characters.
Learn more about bidirectional Unicode characters
This file contains bidirectional Unicode text that may be interpreted or compiled differently than what appears below. To review, open the file in an editor that reveals hidden Unicode characters.
Learn more about bidirectional Unicode characters
Original file line number | Diff line number | Diff line change |
---|---|---|
@@ -1,5 +1,59 @@ | ||
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" |