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• W1635804580 abstract "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 challenged by the complexity of the human genome, including redundancy and the repetitive nature of genome elements and the large amount of variation in individual genomes. Public databases of human genome sequences greatly facilitate interpretation of common and rare genetic variation, although linking database sequence information to detailed clinical information is limited by privacy and practical issues. Genetic variation is a rich source of knowledge for cardiovascular disease because many, if not all, cardiovascular disorders are highly heritable. The role of rare genetic variation in predicting risk and complications of cardiovascular diseases has been well established for hypertrophic and dilated cardiomyopathy, where the number of genes that are linked to these disorders is growing. Bolstered by family data, where genetic variants segregate with disease, rare variation can be linked to specific genetic variation that offers profound diagnostic information. Understanding genetic variation in cardiomyopathy is likely to help stratify forms of heart failure and guide therapy. Ultimately, genetic variation may be amenable to gene correction and gene editing strategies." @default.
• W1635804580 created "2016-06-24" @default.
• W1635804580 creator A5009132358 @default.
• W1635804580 creator A5085872955 @default.
• W1635804580 date "2015-01-01" @default.
• W1635804580 modified "2023-10-03" @default.
• W1635804580 title "Genetic Variation in Cardiomyopathy and Cardiovascular Disorders" @default.
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• W1635804580 doi "https://doi.org/10.1253/circj.cj-15-0536" @default.
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