Article

Whole genome sequencing association analysis of quantitative red blood cell phenotypes: the NHLBI TOPMed program

2020-12-11

Abstract excerpt

Whole genome sequencing (WGS), a powerful tool for detecting novel coding and non-coding disease-causing variants, has largely been applied to clinical diagnosis of inherited disorders. Here we leveraged WGS data in up to 62,653 ethnically diverse participants from the NHLBI Trans-Omics for Precision Medicine (TOPMed) program and assessed statistical association of variants with seven red blood cell (RBC) quantita...

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Literature Corpus work: 09bc1b5a-e1e8-5faa-a7ee-34587ac92315
DOI: 10.1101/2020.12.09.20246736

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