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

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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Bibliographic Details
Main Authors: Mahdieh Labani, Ali Afrasiabi, Amin Beheshti, Nigel H. Lovell, Hamid Alinejad-Rokny
Format: Article
Language:English
Published: Elsevier 2022-01-01
Series:Computational and Structural Biotechnology Journal
Subjects:
Genetic abnormalities
Copy number variations
CNV association study
Risk genes
Artificial intelligence
Online Access:http://www.sciencedirect.com/science/article/pii/S2001037022004068

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http://www.sciencedirect.com/science/article/pii/S2001037022004068

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