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A Groupwise Association Test for Rare Mutations Using a Weighted Sum Statistic
Resequencing is an emerging tool for identification of rare disease-associated mutations. Rare mutations are difficult to tag with SNP genotyping, as genotyping studies are designed to detect common variants. However, studies have shown that genetic heterogeneity is a probable scenario for common di...
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| Huvudupphovsmän: | , |
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| Materialtyp: | Artigo |
| Språk: | Inglês |
| Publicerad: |
Public Library of Science
2009
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| Ämnen: | |
| Länkar: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2633048/ https://ncbi.nlm.nih.gov/pubmed/19214210 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pgen.1000384 |
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