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CNVDeep: deep association of copy number variants with neurocognitive disorders

Abstract Background Copy number variants (CNVs) have become increasingly instrumental in understanding the etiology of all diseases and phenotypes, including Neurocognitive Disorders (NDs). Among the well-established regions associated with ND are small parts of chromosome 16 deletions (16p11.2) and...

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Principais autores: Zahra Rahaie, Hamid R. Rabiee, Hamid Alinejad-Rokny
Format: Artigo
Jezik:Inglês
Izdano: BMC 2024-08-01
Serija:BMC Bioinformatics
Teme:
Copy number variant
Association
Deep learning
Proximal gradient descent
Group LASSO
Autism
Online dostop:https://doi.org/10.1186/s12859-024-05874-8
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