Prioritization Of Nonsynonymous Single Nucleotide Variants For Exome Sequencing Studies Via Integrative Learning On Multiple Genomic Data

The rapid advancement of next generation sequencing technology has greatly accelerated the progress for understanding human inherited diseases via such innovations as exome sequencing. Nevertheless, the identification of causative variants from sequencing data remains a great challenge. Traditional...

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Detalles Bibliográficos
Autores principales: Wu, Mengmeng, Wu, Jiaxin, Chen, Ting, Jiang, Rui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2015
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4602202/
https://www.ncbi.nlm.nih.gov/pubmed/26459872
http://dx.doi.org/10.1038/srep14955

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4602202/
https://www.ncbi.nlm.nih.gov/pubmed/26459872
http://dx.doi.org/10.1038/srep14955

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