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nf-core/sarek

Analysis pipeline to detect germline or somatic variants (pre-processing, variant calling and annotation) from WGS / targeted sequencing
nextflowpipelineworkflownf-coregenomicsvariant-callingbioinformaticsannotationnext-generation-sequencingcondareproducible-researchcancercontainersgermlinesomaticgatk4whole-genome-sequencingwhole-exome-sequencingpre-processingtarget-panels
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  • 470 KB
  • Updated 4 months ago
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Pipeline will be added to your workspace with a full configuration to launch a run using test data.