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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Autori principali:	Zahra Rahaie, Hamid R. Rabiee, Hamid Alinejad-Rokny
Natura:	Artigo
Lingua:	Inglês
Pubblicazione:	BMC 2024-08-01
Serie:	BMC Bioinformatics
Soggetti:	Copy number variant Association Deep learning Proximal gradient descent Group LASSO Autism
Accesso online:	https://doi.org/10.1186/s12859-024-05874-8
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