sarek

Variant detector

Automated workflow for detecting germline or somatic variants in genomic sequencing data

Analysis pipeline to detect germline or somatic variants (pre-processing, variant calling and annotation) from WGS / targeted sequencing

GitHub

409 stars
134 watching
415 forks
Language: Nextflow
last commit: 6 days ago
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annotationbioinformaticscancercondacontainersgatk4genomicsgermlinenext-generation-sequencingnextflownf-corepipelinepre-processingreproducible-researchsomatictarget-panelsvariant-callingwhole-exome-sequencingwhole-genome-sequencingworkflow

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