This repository contains Germline Workflows used for the Kids First Data Resource Center (DRC).
The preeminent workflow in this repository is the Germline Variant Caller Workflow. This all encompassing workflow takes an input BAM/CRAM file and runs all of our production-level calling workflows on it. It will call copy number (CNV), single nucleotide (SNV), and structural variants (SV). Annotation is run on the outputs of the SNV and SV callers.
Complete documentation can be found for the main workflow an its subworkflows here:
While not in our Germline Variant workflow, other workflows potentially useful for germline calling can be found in this repository:
