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Identifying rare and common variants with Bayesian variable selection
BACKGROUND: Recent advances in next-generation sequencing technologies have made it possible to generate large amounts of sequence data with rare variants in a cost-effective way. Yet, the statistical aspect of testing disease association of rare variants is quite challenging as the typical assumpti...
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| Vydáno v: | BMC Proc |
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| Hlavní autor: | |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
BioMed Central
2016
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5133477/ https://ncbi.nlm.nih.gov/pubmed/27980665 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12919-016-0059-0 |
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