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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...
| Autores principales: | , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Nature Publishing Group UK
2017
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| 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 |