search

uclahs-cds / pipeline-call-sSNV

A Nextflow pipeline to identify the somatic single nucleotide variants (sSNVs) by comparing a pair of tumor/normal samples.
https://uclahs-cds.github.io/pipeline-call-sSNV/
GNU General Public License v2.0
5 stars 0 forks source link

standardize input structure #278

Open sorelfitzgibbon opened 8 months ago

sorelfitzgibbon commented 8 months ago

standard structure, allowing BAM or VCF. checking in methods that both are not provided

sorelfitzgibbon commented 8 months ago

vcf:

---
patient_id: 'TWGSAMIN000001'
dataset_id: 'TWGSAMIN'
input_tumor_id: 'S2_v1.1.5' # tumor ID in the VCF files must match this or 'TUMOR'
input_normal_id: 'HG002.N' # normal ID in the VCF files must match this or 'NORMAL'
input:
  VCF:
    muse: /hot/software/pipeline/pipeline-call-sSNV/Nextflow/development/test-input/MuSE-2.0.4_TWGSAMIN_S2-v1.1.5_SNV-pass.vcf.gz
    mutect2: /hot/software/pipeline/pipeline-call-sSNV/Nextflow/development/test-input/Mutect2-4.5.0.0_TWGSAMIN_S2-v1.1.5_all-pass.vcf.gz
    somaticsniper: /hot/software/pipeline/pipeline-call-sSNV/Nextflow/development/test-input/SomaticSniper-1.0.5.0_TWGSAMIN_S2-v1.1.5_hc.vcf.gz
    strelka2: /hot/software/pipeline/pipeline-call-sSNV/Nextflow/development/test-input/Strelka2-2.9.10_TWGSAMIN_S2-v1.1.5_SNV-pass.vcf.gz

bam:

---
patient_id: 'patient_id'
input:
  BAM:
    normal:
      - path: /path/to/normal.bam
    tumor:
      - path: /path/to/tumor.bam
        contamination_table: /path/to/contamination.table