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Clinical Implications of Human Population Differences in Genome-Wide Rates of Functional Genotypes

There have been a number of recent successes in the use of whole genome sequencing and sophisticated bioinformatics techniques to identify pathogenic DNA sequence variants responsible for individual idiopathic congenital conditions. However, the success of this identification process is heavily infl...

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Autores principales: Torkamani, Ali, Pham, Phillip, Libiger, Ondrej, Bansal, Vikas, Zhang, Guangfa, Scott-Van Zeeland, Ashley A., Tewhey, Ryan, Topol, Eric J., Schork, Nicholas J.
Formato: Artigo
Lenguaje:Inglês
Publicado: Frontiers Media S.A. 2012
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Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC3485509/
https://ncbi.nlm.nih.gov/pubmed/23125845
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fgene.2012.00211
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