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A New Method for Detecting Associations with Rare Copy-Number Variants
Copy number variants (CNVs) play an important role in the etiology of many diseases such as cancers and psychiatric disorders. Due to a modest marginal effect size or the rarity of the CNVs, collapsing rare CNVs together and collectively evaluating their effect serves as a key approach to evaluating...
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| Publicat a: | PLoS Genet |
|---|---|
| Autors principals: | , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Public Library of Science
2015
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4592002/ https://ncbi.nlm.nih.gov/pubmed/26431523 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pgen.1005403 |
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