The struggle to find reliable results in exome sequencing data: filtering out Mendelian errors

Next Generation Sequencing studies generate a large quantity of genetic data in a relatively cost and time efficient manner and provide an unprecedented opportunity to identify candidate causative variants that lead to disease phenotypes. A challenge to these studies is the generation of sequencing...

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Main Authors: Patel, Zubin H., Kottyan, Leah C., Lazaro, Sara, Williams, Marc S., Ledbetter, David H., Tromp, hbGerard, Rupert, Andrew, Kohram, Mojtaba, Wagner, Michael, Husami, Ammar, Qian, Yaping, Valencia, C. Alexander, Zhang, Kejian, Hostetter, Margaret K., Harley, John B., Kaufman, Kenneth M.
格式: Artigo
語言:Inglês
出版: Frontiers Media S.A. 2014
主題:
Genetics
在線閱讀:https://ncbi.nlm.nih.gov/pmc/articles/PMC3921572/
https://ncbi.nlm.nih.gov/pubmed/24575121
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fgene.2014.00016
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