variant-calls topic

Repository for the GA4GH Benchmarking Team work developing standardized benchmarking methods for germline small variant calls

ga4gh

🔧 Simple script in python to convert CSV files to VCF

Moduland

Intersect multiple VCF files with haplotype awareness

dancooke

Data management of large-scale whole-genome sequence variant calls (Development version only)

zhengxwen

:snake: DRAGEN Tumor/Normal workflow post-processing

umccr

Bioinformatics on GCP, AWS or Azure

lynnlangit

A flexible, scalable, and reproducible pipeline to automate variant calling from raw sequence reads, with lots of bells and whistles.

moiexpositoalonsolab