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Published in 2019 at "Genetic Epidemiology"
DOI: 10.1002/gepi.22255
Abstract: Both genome‐wide association study and next‐generation sequencing data analyses are widely employed to identify disease susceptible common and/or rare genetic variants. Rare variants generally have large effects though they are hard to detect due to…
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Keywords:
optimally weighted;
common rare;
rare variants;
test ... See more keywords
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Published in 2021 at "Frontiers in Genetics"
DOI: 10.3389/fgene.2021.654804
Abstract: As a pivotal research tool, genome-wide association study has successfully identified numerous genetic variants underlying distinct diseases. However, these identified genetic variants only explain a small proportion of the phenotypic variation for certain diseases, suggesting…
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Keywords:
multiple phenotypes;
hierarchical clustering;
association;
association study ... See more keywords