Imputation of low-coverage sequencing data from 150,119 UK Biobank genomes

rare mutations tag ·

PDF) Imputation of low-coverage sequencing data from 150,119 UK Biobank genomes

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Whole-genome sequencing of half-a-million UK Biobank participants

Whole-genome sequencing of half-a-million UK Biobank participants

Full article: Next-generation sequencing in pharmacogenomics – fit for clinical decision support?

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Frontiers Analyzing the Korean reference genome with meta-imputation increased the imputation accuracy and spectrum of rare variants in the Korean population

Scientific publications 2022 SIB Swiss Institute of Bioinformatics

Evolutionary Trends of Polygenic Scores in European Populations From the Paleolithic to Modern Times, Twin Research and Human Genetics