Article

ClinCNV: novel method for allele-specific somatic copy-number alterations detection

2019-11-11

Abstract excerpt

<h4>Motivation</h4> Large somatic copy number alterations (CNA), short indels and single nucleotide variants (SNVs) are playing important role in cancer development and can serve as a predictor for targeted therapy selection as well as prognostic factor. Genomic microarrays, FISH, MLPA and many other technologies are widely used for detection of CNAs. Whole-genome sequencing (WGS), whole-exome sequencing (WES) an...

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Literature Corpus work: 79c2480d-2fde-5e03-9c12-6509b0816824
DOI: 10.1101/837971

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