snvs topic

Personal Cancer Genome Reporter (PCGR)

sigven

Strelka2 germline and somatic small variant caller

Illumina

Microassembly based somatic variant caller for NGS data

nygenome

A method for variant graph genotyping based on exact alignment of k-mers

bioinformatics-centre

The Platinum Genomes Truthset

Illumina

Generic human DNA variant annotation pipeline

sigven

ClairS - a deep-learning method for long-read somatic small variant calling

HKU-BAL

ClairS-TO - a deep-learning method for tumor-only somatic variant calling

HKU-BAL

SNV calling from single cell sequencing

KChen-lab