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Powerful and efficient SNP-set association tests across multiple phenotypes using GWAS summary data

MOTIVATION: Many GWAS conducted in the past decade have identified tens of thousands of disease related variants, which in total explained only part of the heritability for most traits. There remain many more genetics variants with small effect sizes to be discovered. This has motivated the developm...

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Bibliografski detalji
Izdano u:Bioinformatics
Glavni autori: Guo, Bin, Wu, Baolin
Format: Artigo
Jezik:Inglês
Izdano: Oxford University Press 2019
Teme:
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC6477978/
https://ncbi.nlm.nih.gov/pubmed/30239606
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/bioinformatics/bty811
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