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Fuzzy methods for the detection of copy number variations in comparative genomic hybridization arrays

Genomic copy number variations (CNVs) are considered as a significant source of genetic diversity and widely involved in gene expression and regulatory mechanism, genetic disorders and disease risk, susceptibility to certain diseases and conditions, and resistance to medical drugs. Many studies have...

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Bibliografski detalji
Izdano u:Saudi J Biol Sci
Glavni autori: AlShibli, Ahmad, Mathkour, Hassan
Format: Artigo
Jezik:Inglês
Izdano: Elsevier 2020
Teme:
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC7714972/
https://ncbi.nlm.nih.gov/pubmed/33304176
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.sjbs.2020.08.007
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