Leveraging multiple genomic data to prioritize disease-causing indels from exome sequencing data

The emergence of exome sequencing in recent years has enabled rapid and cost-effective detection of genetic variants in coding regions and offers a great opportunity to combine sequencing experiments with subsequent computational analysis for dissecting genetic basis of human inherited diseases. How...

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Detalles Bibliográficos
Autores principales: Wu, Mengmeng, Chen, Ting, Jiang, Rui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5431795/
https://www.ncbi.nlm.nih.gov/pubmed/28496131
http://dx.doi.org/10.1038/s41598-017-01834-w

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5431795/
https://www.ncbi.nlm.nih.gov/pubmed/28496131
http://dx.doi.org/10.1038/s41598-017-01834-w

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