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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Autors principals:	Zahra Rahaie, Hamid R. Rabiee, Hamid Alinejad-Rokny
Format:	Artigo
Idioma:	Inglês
Publicat:	BMC 2024-08-01
Col·lecció:	BMC Bioinformatics
Matèries:	Copy number variant Association Deep learning Proximal gradient descent Group LASSO Autism
Accés en línia:	https://doi.org/10.1186/s12859-024-05874-8
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