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Article

CNV Radar: an improved method for somatic copy number alteration characterization in oncology.

BMC bioinformatics - 6 Mar 2020

Soong David, Stratford Jeran, Avet-Loiseau Herve, Bahlis Nizar, Davies Faith, Dispenzieri Angela, Sasser A Kate, Schecter Jordan M, Qi Ming, Brown Chad, Jones Wendell, Keats Jonathan J, Auclair Daniel, Chiu Christopher, Powers Jason, Schaffer Michael

Abstract excerpt

BACKGROUND: Cancer associated copy number variation (CNV) events provide important information for identifying patient subgroups and suggesting treatment strategies. Technical and logistical issues, however, make it challenging to accurately detect abnormal copy number events in a cost-effective manner in clinical studies. RESULTS: Here we present CNV Radar, a software tool that utilizes next-generation...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 32143562
DOI: 10.1186/s12859-020-3397-x
PMCID: PMC7060549

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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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