Bi-stream CNN Down Syndrome screening model based on genotyping array

BACKGROUND: Human Down syndrome (DS) is usually caused by genomic micro-duplications and dosage imbalances of human chromosome 21. It is associated with many genomic and phenotype abnormalities. Even though human DS occurs about 1 per 1,000 births worldwide, which is a very high rate, researchers ha...

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Detalles Bibliográficos
Autores principales: Feng, Bing, Hoskins, William, Zhang, Yan, Meng, Zibo, Samuels, David C., Wang, Jiandong, Xia, Ruofan, Liu, Chao, Tang, Jijun, Guo, Yan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6245487/
https://www.ncbi.nlm.nih.gov/pubmed/30453947
http://dx.doi.org/10.1186/s12920-018-0416-0

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6245487/
https://www.ncbi.nlm.nih.gov/pubmed/30453947
http://dx.doi.org/10.1186/s12920-018-0416-0

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