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08db860938
* initial commit to setup branch * workflow finished * Update nextflow.config * tumour to tumor, getpileup passed as nomral and tumor * paired_somatic renamed to tumor_normal_somatic * Apply suggestions from code review Co-authored-by: Maxime U. Garcia <maxime.garcia@scilifelab.se> * Update subworkflows/nf-core/gatk_tumor_normal_somatic_variant_calling/main.nf Co-authored-by: Maxime U. Garcia <maxime.garcia@scilifelab.se> * updated index names in meta.yml * changed index file names in main script and test * Apply suggestions from code review Co-authored-by: Maxime U. Garcia <maxime.garcia@scilifelab.se> * Apply suggestions from code review * fixed bug from changes * Apply suggestions from code review * modified yml to allow new subworkflow testing * Update test.yml * Update test.yml * updated to follow the new mergebam syntax, also made unaligned input sample specific Co-authored-by: GCJMackenzie <gavin.mackenzie@nibsc.org> Co-authored-by: Maxime U. Garcia <maxime.garcia@scilifelab.se> |
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applybqsr | ||
applyvqsr | ||
baserecalibrator | ||
bedtointervallist | ||
calculatecontamination | ||
createsequencedictionary | ||
createsomaticpanelofnormals | ||
estimatelibrarycomplexity | ||
fastqtosam | ||
filtermutectcalls | ||
gatherbqsrreports | ||
genomicsdbimport | ||
genotypegvcfs | ||
getpileupsummaries | ||
haplotypecaller | ||
indexfeaturefile | ||
intervallisttools | ||
learnreadorientationmodel | ||
markduplicates | ||
mergebamalignment | ||
mergevcfs | ||
mutect2 | ||
revertsam | ||
samtofastq | ||
splitncigarreads | ||
variantfiltration | ||
variantrecalibrator |