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Chunk #45 — Discussion

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A saturated map of common genetic variants associated with human height.
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study, ideally using methods that can accommodate dense sets of signals and large populations with African ancestries, would substantially improve the accuracy of a derived height PGS for populations of non-European ancestry. Our study has a large number of participants with African ancestries as compared with previous efforts. However, we emphasize that further increasing the size of GWASs in populations of non-European ancestry, including those with diverse African ancestries, is essential to bridge the gap in prediction accuracy—particularly as most studies only partially capture the wide range of ancestral diversity both within Africa and globally. Such increased sample sizes would help to identify potential ancestry-specific causal variants, to facilitate ancestry-specific fine-mapping and to inform gene–environment and gene–ancestry interactions. Another important finding of our study is to show how individual PGS can be optimally combined with familial information and thereby improve the overall accuracy of height prediction to above 54% in populations of European ancestry.