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Exome genotyping arrays to identify rare and low frequency variants associated with epithelial ovarian cancer risk
Rare and low frequency variants are not well covered in most germline genotyping arrays and are understudied in relation to epithelial ovarian cancer (EOC) risk. To address this gap, we used genotyping arrays targeting rarer protein-coding variation in 8,165 EOC cases and 11,619 controls from the in...
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Publicado no: | Hum Mol Genet |
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Main Authors: | , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
Formato: | Artigo |
Idioma: | Inglês |
Publicado em: |
Oxford University Press
2016
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Assuntos: | |
Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5179948/ https://ncbi.nlm.nih.gov/pubmed/27378695 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddw196 |
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