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Article

Joint genotype inference with germline and somatic mutations.

BMC bioinformatics - 1 Jan 2013

Bareke Eric, Saillour Virginie, Spinella Jean-François, Vidal Ramon, Healy Jasmine, Sinnett Daniel, Csűrös Miklós

Abstract excerpt

The joint sequencing of related genomes has become an important means to discover rare variants. Normal-tumor genome pairs are routinely sequenced together to find somatic mutations and their associations with different cancers. Parental and sibling genomes reveal de novo germline mutations and i...

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Identifiers

PMID: 23734724
DOI: 10.1186/1471-2105-14-S5-S3
PMCID: PMC3622648

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-23734724-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

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