macarthur-lab / gnomad_mnvLinks
Multi-nucleotide variants (MNVs) in gnomAD 2.1
☆12Updated 3 years ago
Alternatives and similar repositories for gnomad_mnv
Users that are interested in gnomad_mnv are comparing it to the libraries listed below
Sorting:
- Example datasets for CNVkit (http://github.com/etal/cnvkit)☆23Updated 6 years ago
- Structural variant VCF annotation, duplicate removal and comparison☆33Updated 5 months ago
- Suite of tools for analysing off-target reads to find CNVs, homozygous regions, and shared haplotypes