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

Abstract 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 dise...

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Autores principales: Mengmeng Wu, Ting Chen, Rui Jiang
Formato: article
Lenguaje:EN
Publicado: Nature Portfolio 2017
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Acceso en línea:https://doaj.org/article/5903d74ef19c4ff9ae3629c378363231
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