Publications
View AllImproved 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 (...
Affiliated Researchers
Institution Info
- Type
- healthcare
- Country
- IT
- Publications
- 2
- Citations
- 3,495
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- ROR
- https://ror.org/03t1jzs40