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Chunk #39 — Methods — Additional quality control

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Rare variant contribution to human disease in 281,104 UK Biobank exomes.
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To mitigate a possible increase of variance estimates due to relatedness, we sought to remove related individuals from our analyses. Using exome sequence-derived genotypes for 43,889 biallelic autosomal SNVs located in coding regions as input to the kinship algorithm included in KING v2.2.353, we generated pairwise kinship coefficients for all remaining samples.