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Article

Single-Nucleotide Polymorphism to Associate Cancer Risk.

Methods in molecular biology (Clifton, N.J.) - 1 Jan 2016

Shaw Victoria, Bullock Katie, Greenhalf William

Abstract excerpt

Genetic heterogeneity explains variation in predisposition for cancer. Whole-genome analysis allows risk to be quantified, giving better targeted screening and quantification of the personalized risk posed by environmental factors. Array-based approaches to whole-genome analysis are rapidly being overtaken by next-generation sequencing (NGS). In this review the different platforms currently available for NGS are...

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PMID: 26667457
DOI: 10.1007/978-1-4939-3204-7_6

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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