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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...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Julkaisussa:Circ J
Päätekijät: McNally, Elizabeth M., Puckelwartz, Megan J.
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: 2015
Aiheet:
Linkit: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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