Twelve years of SAMtools and BCFtools
Abstract Background SAMtools and BCFtools are widely used programs for processing and analysing high-throughput sequencing data. They include tools for file format conversion an...
Publications
3 shownImproved imputation of low-frequency and rare variants using the UK10K haplotype reference panel
Abstract Imputing genotypes from reference panels created by whole-genome sequencing (WGS) provides a cost-effective strategy for augmenting the single-nucleotide polymorphism (...
Frequent Co-Authors
Researcher Info
- h-index
- 3
- Publications
- 3
- Citations
- 16,575
- Institution
- Wellcome Sanger Institute
External Links
Identifiers
- ORCID
- 0000-0002-2715-4187
Impact Metrics
h-index
3
h-index: Number of publications with at least h citations each.