Table S5 from Predicting Cancer Risk from Germline Whole-exome Sequencing Data Using a Novel Context-based Variant Aggregation Approach

dataset

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

<p>Table S5: Significant predictors from individual association analyses based on SNP array data. The significance threshold for each cancer type was 0.05/2824 (2824 predictors were tested for each cancer type).</p>

Funding

HHS | NIH | National Cancer Institute (NCI)

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DOI - Is supplement to Predicting Cancer Risk from Germline Whole-exome Sequencing Data Using a Novel Context-based Variant Aggregation Approach

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.