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New preprint on exome imputation and fine-mapping in UK Biobank

We are excited to share a new preprint, " Whole-exome imputation within UK Biobank powers rare coding variant association and fine-mapping analyses" (Barton et al.), which reports an atlas of 1,189 rare coding variants likely to causally influence 54 quantitative traits in UK Biobank. This analysis...

Data

CNV-phenotype associations for 56 quantitative traits in UK Biobank Hujoel et al. 2022 CellThis data set contains full association statistics from BOLT-LMM analysis of categories of CNVs called in the UK Biobank cohort using HI-CNV to perform haplotype-informed CNV detection from SNP-array...