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nf-core/sarek
Edit

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

annotationcancergatk4genomicsgermlinepre-processingsomatictarget-panelsvariant-callingwhole-exome-sequencingwhole-genome-sequencing
This is the development version of the pipeline.
Launch development version https://github.com/nf-core/sarek
  • Introduction
  • Usage
  • Parameters
  • Output
  • Releases
    • 3.7.1
    • 3.7.0
    • 3.6.1
    • 3.6.0
    • 3.5.1
    • 3.5.0
    • 3.4.4
    • 3.4.3
    • 3.4.2
    • 3.4.1
    • 3.4.0
    • 3.3.2
    • 3.3.1
    • 3.3.0
    • 3.2.3
    • 3.2.2
    • 3.2.1
    • 3.2.0
    • 3.1.2
    • 3.1.1
    • 3.1
    • 3.0.2
    • 3.0.1
    • 3.0
    • 2.7.2
    • 2.7.1
    • 2.7
    • 2.6.1
    • 2.6
    • 2.5.2
    • 2.5.1
    • 2.5
    • dev
Introduction Usage Parameters Output Releases
  • 3.7.1
  • 3.7.0
  • 3.6.1
  • 3.6.0
  • 3.5.1
  • 3.5.0
  • 3.4.4
  • 3.4.3
  • 3.4.2
  • 3.4.1
  • 3.4.0
  • 3.3.2
  • 3.3.1
  • 3.3.0
  • 3.2.3
  • 3.2.2
  • 3.2.1
  • 3.2.0
  • 3.1.2
  • 3.1.1
  • 3.1
  • 3.0.2
  • 3.0.1
  • 3.0
  • 2.7.2
  • 2.7.1
  • 2.7
  • 2.6.1
  • 2.6
  • 2.5.2
  • 2.5.1
  • 2.5
  • dev
run with
See the docs on how to configure the Seqera Platform CLI.
  • nf-core
  • Nextflow
  • Seqera Platform
video introduction
Play
subscribers
144
stars
538
open issues
344
open PRs
30
last release
about 2 months ago
last update
about 2 months ago
included modules
ascatbbmap_bbsplitbcftools_annotatebcftools_concatbcftools_isec and 112 more modules
included subworkflows
bam_ngscheckmateutils_nextflow_pipelineutils_nfcore_pipelineutils_nfschema_pluginvcf_annotate_ensemblvep and 1 more subworkflow
contributors
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