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Detecting Multiethnic Rare Variants

Genome-wide association studies have identified many common genetic variants which are associated with certain diseases. The identified common variants, however, explain only a small portion of the heritability of a complex disease phenotype. The missing heritability motivated researchers to test th...

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Bibliografski detalji
Izdano u:Methods Mol Biol
Glavni autori: Ouyang, Weiwei, Zhu, Xiaofeng, Qin, Huaizhen
Format: Artigo
Jezik:Inglês
Izdano: 2017
Teme:
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC6350776/
https://ncbi.nlm.nih.gov/pubmed/28980263
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/978-1-4939-7274-6_26
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