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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Detalles Bibliográficos
Autores principales: AlShibli, Ahmad, Mathkour, Hassan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7714972/
https://www.ncbi.nlm.nih.gov/pubmed/33304176
http://dx.doi.org/10.1016/j.sjbs.2020.08.007

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7714972/
https://www.ncbi.nlm.nih.gov/pubmed/33304176
http://dx.doi.org/10.1016/j.sjbs.2020.08.007

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