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ClearSeq Cardiomyopathy, HS, ILM

RUO

​The ClearSeq Cardiomyopathy HS is a next generation sequencing target enrichment panel designed specifically for inherited forms of cardiomyopathy. Following a careful review of cardiomyopathy publications as well as information available from GeneReviews, an NIH online resource, 34 genes known to be associated with hypertrophic cardiomyopathy, dilated cardiomyopathy, and arrythmogenic right ventricular cardiomyopathy have been included. These panels are compatible with HaloPlexHS, providing faster results and limited sample compatibility (high throughput or benchtop sequencers)
The ClearSeq constitutional research panels are catalog designs focused on targeted gene sets for comprehensive detection of mutations, indels, and CNVs in rare disease pathogenesis. The panels’ optimized content contains target regions identified by leading research institutions.
For Research Use Only. Not for use in diagnostic procedures.

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