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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...
Tallennettuna:
| Julkaisussa: | Circ J |
|---|---|
| Päätekijät: | , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
2015
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| 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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