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