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Article

Computational methods and resources for the interpretation of genomic variants in cancer.

BMC genomics - 1 Jan 2015

Tian Rui, Basu Malay K, Capriotti Emidio

Abstract excerpt

The recent improvement of the high-throughput sequencing technologies is having a strong impact on the detection of genetic variations associated with cancer. Several institutions worldwide have been sequencing the whole exomes and or genomes of cancer patients in the thousands, thereby providing an invaluable collection of new somatic mutations in different cancer types. These initiatives promoted the...

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PMID: 26111056
DOI: 10.1186/1471-2164-16-S8-S7
PMCID: PMC4480958

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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