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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...
Tallennettuna:
| Julkaisussa: | Bioinformatics |
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| Päätekijät: | , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
Oxford University Press
2019
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| Aiheet: | |
| Linkit: | 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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