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Comparing family-based rare variant association tests for dichotomous phenotypes
BACKGROUND: It has been repeatedly stressed that family-based samples suffer less from genetic heterogeneity and that association analyses with family-based samples are expected to be powerful for detecting susceptibility loci for rare disease. Various approaches for rare-variant analysis with famil...
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| Pubblicato in: | BMC Proc |
|---|---|
| Autori principali: | , , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
BioMed Central
2016
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5133528/ https://ncbi.nlm.nih.gov/pubmed/27980633 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12919-016-0027-8 |
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