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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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Enregistré dans:
Détails bibliographiques
Publié dans:Circ J
Auteurs principaux: McNally, Elizabeth M., Puckelwartz, Megan J.
Format: Artigo
Langue:Inglês
Publié: 2015
Sujets:
Accès en ligne: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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