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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...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Elsevier
2020
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| 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 |