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Genetic variation in cardiomyopathy and cardiovascular disorders

With the wider deployment of massively parallel, next generation sequencing, it is now possible to survey human genome data for research and clinical purposes. The reduced cost of producing short read sequencing has now shifted the burden to data analysis. Analysis of genome sequencing remains chall...

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Detalles Bibliográficos
Publicado en:Circ J
Main Authors: McNally, Elizabeth M., Puckelwartz, Megan J.
Formato: Artigo
Idioma:Inglês
Publicado: 2015
Assuntos:
Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC4605546/
https://ncbi.nlm.nih.gov/pubmed/26040335
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1253/circj.CJ-15-0536
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