gatk3-4-rnaseq-germline-snps-indels
GATK3 and this workflow is now longer supported, this repo is intended for legacy purposes. Pleas visit gatk4-rnaseq-germline-snps-indels for the latest version of the workflow
Workflows for processing RNA data for germline short variant discovery with GATK (v3+v4) and related tools
Requirements/expectations :
- BAM
Output :
- A BAM file and its index.
- A VCF file and its index.
- A Filtered VCF file and its index.
Runtime parameters are optimized for Broad's Google Cloud Platform implementation. For program versions, see docker containers.
Important Note :
- The workflow allows users to opt to use GATK4 for all tools instead of the default combination between GATK3 and GATK4, but note the workflow has not been validated to run using all GATK4 tools.
- Runtime parameters are optimized for Broad's Google Cloud Platform implementation.
- For help running workflows on the Google Cloud Platform or locally please view the following tutorial (How to) Execute Workflows from the gatk-workflows Git Organization
LICENSING :
This script is released under the WDL source code license (BSD-3) (see LICENSE in https://github.com/broadinstitute/wdl). Note however that the programs it calls may be subject to different licenses. Users are responsible for checking that they are authorized to run all programs before running this script. Please see the docker page at https://hub.docker.com/r/broadinstitute/genomes-in-the-cloud/ for detailed licensing information pertaining to the included programs.