There are 1 repository under variant-calls topic.
Repository for the GA4GH Benchmarking Team work developing standardized benchmarking methods for germline small variant calls
A flexible, scalable, and reproducible pipeline to automate variant calling from sequence reads.
Bioinformatics on GCP, AWS or Azure
PySeqArray: data manipulation of whole-genome sequencing variants with SeqArray files in Python (pre-release version)
An implementation of a generic ArrayList and a generic LinkedList in cpp which can store multiple data type variables.
COVID-19 Variants Repository
From second generation sequencing reads to variant calls