Statistical phasing of 150,119 sequenced genomes in the UK Biobank
Author:
Funder
National Human Genome Research Institute
National Institutes of Health
Publisher
Elsevier BV
Subject
Genetics (clinical),Genetics
Reference17 articles.
1. The sequences of 150, 119 genomes in the UK Biobank;Halldorsson;Nature,2022
2. Fast and accurate genotype imputation in genome-wide association studies through pre-phasing;Howie;Nat. Genet.,2012
3. RFMix: a discriminative modeling approach for rapid and robust local-ancestry inference;Maples;Am. J. Hum. Genet.,2013
4. Benchmarking relatedness inference methods with genome-wide data from thousands of relatives;Ramstetter;Genetics,2017
5. A fast and simple method for detecting identity-by-descent segments in large-scale data;Zhou;Am. J. Hum. Genet.,2020
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1. A Genomics England haplotype reference panel and imputation of UK Biobank;Nature Genetics;2024-08-12
2. Improving population scale statistical phasing with whole-genome sequencing data;PLOS Genetics;2024-07-03
3. Analysis-ready VCF at Biobank scale using Zarr;2024-06-12
4. Simultaneous estimation of genotype error and uncalled deletion rates in whole genome sequence data;PLOS Genetics;2024-05-24
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