X-CNV: genome-wide prediction of the pathogenicity of copy number variations

BACKGROUND: Gene copy number variations (CNVs) contribute to genetic diversity and disease prevalence across populations. Substantial efforts have been made to decipher the relationship between CNVs and pathogenesis but with limited success. RESULTS: We have developed a novel computational framework...

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Detalles Bibliográficos
Autores principales: Zhang, Li, Shi, Jingru, Ouyang, Jian, Zhang, Riquan, Tao, Yiran, Yuan, Dongsheng, Lv, Chengkai, Wang, Ruiyuan, Ning, Baitang, Roberts, Ruth, Tong, Weida, Liu, Zhichao, Shi, Tieliu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Software
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8375180/
https://www.ncbi.nlm.nih.gov/pubmed/34407882
http://dx.doi.org/10.1186/s13073-021-00945-4

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8375180/
https://www.ncbi.nlm.nih.gov/pubmed/34407882
http://dx.doi.org/10.1186/s13073-021-00945-4

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