CNVIntegrate: the first multi-ethnic database for identifying copy number variations associated with cancer

Human copy number variations (CNVs) and copy number alterations (CNAs) are DNA segments (>1000 base pairs) of duplications or deletions with respect to the reference genome, potentially causing genomic imbalance leading to diseases such as cancer. CNVs further cause genetic diversity in healthy p...

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Detalles Bibliográficos
Autores principales: Chattopadhyay, Amrita, Teoh, Zi Han, Wu, Chi-Yun, Juang, Jyh-Ming Jimmy, Lai, Liang-Chuan, Tsai, Mong-Hsun, Wu, Chia-Hsin, Lu, Tzu-Pin, Chuang, Eric Y
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8278790/
https://www.ncbi.nlm.nih.gov/pubmed/34259866
http://dx.doi.org/10.1093/database/baab044

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8278790/
https://www.ncbi.nlm.nih.gov/pubmed/34259866
http://dx.doi.org/10.1093/database/baab044

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