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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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發表在: | Hum Mol Genet |
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Main Authors: | , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
格式: | Artigo |
語言: | Inglês |
出版: |
Oxford University Press
2016
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主題: | |
在線閱讀: | 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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