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A nextflow pipeline for calling and annotating small germline variants from short DNA reads for WES and WGS data

Home Page: https://nf-cmgg.github.io/germline/

License: MIT License

HTML 0.93% Nextflow 94.60% Groovy 4.08% Dockerfile 0.39%
annotation cram genotyping germline germline-variant-calling ngs ngs-pipeline short-reads

germline's Introduction

GitHub Actions CI Status GitHub Actions Linting Status nf-test

Nextflow run with conda run with docker run with singularity Launch on Seqera Platform

Introduction

nf-cmgg/germline is a nextflow pipeline for calling and annotating small germline variants from short DNA reads for WES and WGS data.

The pipeline is built using Nextflow, a workflow tool to run tasks across multiple compute infrastructures in a very portable manner. It uses Docker/Singularity containers making installation trivial and results highly reproducible. The Nextflow DSL2 implementation of this pipeline uses one container per process which makes it much easier to maintain and update software dependencies. Where possible, these processes have been submitted to and installed from nf-core/modules in order to make them available to all nf-core pipelines, and to everyone within the Nextflow community!

Please have a look at the documentation on how to run the pipeline.

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