Chunk #47 — Methods — High-coverage whole-exome sequencing in BioMe study

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Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program.

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We further removed variants with call rate <99% (that is, missing in more than 10 individuals), reducing the number of analysed autosomal variants to 1,044,517. The comparison results of TOPMed WGS and BioMe WES data are described in Supplementary Information 1.3.1.