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Table S1 from Predicting Cancer Risk from Germline Whole-exome Sequencing Data Using a Novel Context-based Variant Aggregation Approach

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posted on 2023-04-04, 02:21 authored by Zoe Guan, Colin B. Begg, Ronglai Shen

Table S1: Known risk genes (from Rahman 2014) and SNPs (from NHGRI-EBI GWAS Catalog) in WES models.

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HHS | NIH | National Cancer Institute (NCI)

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ARTICLE ABSTRACT

There is evidence that cancer is partly caused by rare genetic variants that have not yet been identified. We investigate this issue using novel statistical methods and data from the UK Biobank.

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    Cancer Research Communications

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