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Association score testing for rare variants and binary traits in family data with shared controls
Genome-wide association studies have been an important approach used to localize trait loci, with primary focus on common variants. The multiple rare variant–common disease hypothesis may explain the missing heritability remaining after accounting for identified common variants. Advances of sequenci...
Tallennettuna:
| Julkaisussa: | Brief Bioinform |
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| Päätekijät: | , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
Oxford University Press
2017
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6357552/ https://ncbi.nlm.nih.gov/pubmed/28968627 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/bib/bbx107 |
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