ClearSeq Arrythmia

ClearSeq 心律不整相關基因研究


Targeting genomic regions known to be associated with four inherited arrhythmia related heart disorders, ClearSeq Arrhythmia is a next generation sequencing target enrichment panel. Included are 20 genes known to correlate with long QT syndrome, short QT syndrome, Brugada syndrome, and catecholaminergic polymorphic ventricular tachycardia, developed from information gathered after a thorough review of publications for arrhythmia and from GeneReviews, an NIH resource. The genes associated with different types of arrhythmia are overlapping in some cases, and using ClearSeq Arrhythmia, a comprehensive arrhythmia profile can be assembled for clinical research samples.Compatible with HaloPlexHS and HaloPlex Target Enrichment Systems

ClearSeq Arrythmia

Target genomic regions in 20 genes known to be linked to four inherited arrhythmia-related heart disordersCompatible with HaloPlex

產品列表

貨號 產品 數量
G9954C ClearSeq Made-to-Order Panels, HS 48 rxns
G9954B ClearSeq Made-to-Order Panels, HS 96 rxns
G9953C ClearSeq Made-to-Order Panels 48 rxns
G9953B ClearSeq Made-to-Order Panels 96 rxns

ClearSeq Arrythmia

  • Expert-optimized content - Highly targeted content enabling analysis of regions implicated in rare disease pathogenesis
  • Fast track to answers - Proven, high-performing capture oligos are coupled with highly efficient SureSelect and HaloPlex workflows, providing faster time to results and compatibility with samples of limited availability (high throughput or benchtop sequencers)
  • Comprehensive Workflow Solution - Accelerated sample to categorized variants with SureCall
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