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Article

SNVSniffer: an integrated caller for germline and somatic single-nucleotide and indel mutations.

BMC systems biology - 1 Aug 2016

Liu Yongchao, Loewer Martin, Aluru Srinivas, Schmidt Bertil

Abstract excerpt

BACKGROUND: Various approaches to calling single-nucleotide variants (SNVs) or insertion-or-deletion (indel) mutations have been developed based on next-generation sequencing (NGS). However, most of them are dedicated to a particular type of mutation, e.g. germline SNVs in normal cells, somatic SNVs in cancer/tumor cells, or indels only. In the literature, efficient and integrated callers for both germline and...

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Identifiers

PMID: 27489955
DOI: 10.1186/s12918-016-0300-5
PMCID: PMC4977481

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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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