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Chunk #76 — Methods — Evolutionary genetics of individuals with diverse ancestry — Selection

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Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program.
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population. We analysed each population separately. Only bi-allelic sites with an unambiguous ancestral state, inferred using the WGSA pipeline108, were used. Sites near chromosome boundaries, near centromeres and in regions with poor accessibility were excluded. We used the previously published R scripts61 to perform all demographic history simulations and SDS computations in each population. We then normalized raw SDS scores within 1% frequency bins and treated the normalized scores as Z-scores to convert them to P values as described previously61. Raw and normalized SDS scores are included in Supplementary Data 2.