- DeepVariant quick start
- DeepVariant whole genome case study
- DeepVariant exome case study
- DeepVariant PacBio case study
- Best practices for multi-sample variant calling
- Advanced Case Study: Train a customized SNP and small indel variant caller for BGISEQ-500 data
- DeepVariant training data
- DeepVariant usage guide
- Building and testing DeepVariant
- DeepVariant Genomic VCF (gVCF) support
- Getting Started with GCP (It is not required to run DeepVariant on GCP.)
- VCF stats report