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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...
Guardat en:
| Publicat a: | Saudi J Biol Sci |
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| Autors principals: | , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Elsevier
2020
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| Matèries: | |
| Accés en línia: | 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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