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Inherited CardioKitDx

Protocol automated using Magnis NGS Prep System

Description

Study of genetic alterations related to cardiomyopathies, arrhythmias (channelopathies), and sudden death

Format

16 rxn

Technology

NGS sequencing

Reference

IMG-390

Compatible equipment

Libraries preparation: Magnis NGS Prep System (Agilent); Sequencing: NextSeq 500/550Dx System

Protocol automated using Magnis NGS Prep System
Kit Health in Code
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  • Dynamic kit that updates the target genes of the panel according to scientific evidence.
  • SNV and indel analysis in genes with full exonic regions and intronic regions of interest, as well as CNV analysis
  • STIDs can be included: Integrated sample identification and tracking system.
  • Coverage: 99.8% of bases covered at 30X minimum depth.
  • Uniformity: 99.1% of bases covered at >20% mean coverage.
  • Sensitivity: > 99.9%.
  • Specificity: > 99%.
  • Repeatability: > 99.9%.
  • Reproducibility: >99.9%.
  • Analysis software included: Data Genomics.
  • For in vitro diagnostic use only.

Inherited CardioKitDx employs a fully automated technology for library preparation and selection of regions of interest by hybridization with capture probes. Subsequently, massive sequencing is carried out on Illumina platforms.

  • Compatible sequencers: NextSeq 500/550Dx System
  • Number of reactions: 16
  • Number of samples per run: Mid Output v2.5 kit (150 cycles): 16 samples
  • Sequencing: Paired-end (2×75 cycles).
  • Amount of input DNA: 200 ng.
  • Genomic region analyzed: 1.86 Mb
  • Sample type: DNA from peripheral blood
Inherited CardioKitDx: Instructions for use
Inherited CardioKitDx: MSDS
Analysis certificate

Inherited CardioKitDx

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