This is sankemake-wrapper of variant calling workflow using DeepVariant.
yiolino
- Create a new github repository using this workflow as a template.
- Clone the newly created repository to your local system, into the place where you want to perform the data analysis.
$ git clone https://github.com/tetsuro90/snakemake-deepvariant.git
An example is shown below.
sample platform fq1 fq2
SRR1770413 ILLUMINA data/reads/SRR1770413_1.fastq.gz data/reads/SRR1770413_2.fastq.gz
SRR341549 ILLUMINA data/reads/SRR341549_1.fastq.gz data/reads/SRR341549_2.fastq.gz
sample
SRR1770413
SRR341549
$ cd snakmake-deepvariant/
$ docker-compose up -d
$ docker exec -it deepvariant /bin/bash
$ cd working/
$ snakemake -j {#CORE} --use-conda all
Once the workflow has been successfully completed, you can output a report file.
$ snakemake --report
MIT License
- DeepVariant. Copyright 2017 Google LLC. BSD-3-Clause license.
- DeepVariant bioconda package. Copyright 2018 Brad Chapman. MIT license.
- Snakemake workflow: dna-seq-gatk-variant-calling. Copyright 2018, Johannes Köster. MIT license.
- fastp. Copyright 2017 OpenGene - Open Source Genetics Toolbox. MIT license.
- samtools. Copyright 2008-2019 Genome Research Ltd. The MIT/Expat License.
- gatk-lite. Copyright Broad Institue, Inc. MIT license.
- gatk4. Copyright 2009-2020, Broad Institute, Inc. BSD-3-Clause license.
- bwa. Copyright 2009, Li H. and Durbin R. GPLv3 License.