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Successful identification of rare variants using oligogenic segregation analysis as a prioritizing tool for whole-exome sequencing studies

We aim to identify rare variants that have large effects on trait variance using a cost-efficient strategy. We use an oligogenic segregation analysis as a prioritizing tool for whole-exome sequencing studies to identify families more likely to harbor rare variants, by estimating the mean number of q...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Egile Nagusiak: Gagnon, France, Roslin, Nicole M, Lemire, Mathieu
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: BioMed Central 2011
Gaiak:
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC3287833/
https://ncbi.nlm.nih.gov/pubmed/22373114
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1753-6561-5-S9-S11
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