PeakCNV: A multi-feature ranking algorithm-based tool for genome-wide copy number variation-association study

Copy Number Variation (CNV) refers to a type of structural genomic alteration in which a segment of chromosome is duplicated or deleted. To date, many CNVs have been identified as causative genetic elements for several diseases and phenotypes. However, performing a CNV-based genome-wide association...

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Detalles Bibliográficos
Autores principales: Labani, Mahdieh, Afrasiabi, Ali, Beheshti, Amin, Lovell, Nigel H., Alinejad-Rokny, Hamid
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Research Network of Computational and Structural Biotechnology 2022
Materias:
Method Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9478359/
https://www.ncbi.nlm.nih.gov/pubmed/36147666
http://dx.doi.org/10.1016/j.csbj.2022.09.001

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9478359/
https://www.ncbi.nlm.nih.gov/pubmed/36147666
http://dx.doi.org/10.1016/j.csbj.2022.09.001

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