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novoSNP3: variant detection and sequence annotation in resequencing projects.

Methods in molecular biology (Clifton, N.J.) - 1 Jan 2007

Rijk Peter De, Del-Favero Jurgen

Abstract excerpt

The same high-throughput techniques used to make genomic sequences generally available, are also useful in mapping the genetic differences between individuals. Resequencing of a genomic region in a set of individuals is considered the golden standard for the discovery of sequence variants. However, with the available high-throughput sequencing technology data analysis has become the rate-limiting step in data...

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PMID: 18025702
DOI: 10.1007/978-1-59745-515-2_21

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

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