GTR Home > Tests > Cardiac Arrhythmia NGS Multi-Gene Panel (48 genes), Sequence & CNV analysis

Overview

Test name

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Cardiac Arrhythmia NGS Multi-Gene Panel (48 genes), Sequence & CNV analysis

Purpose of the test

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This is a clinical test intended for Help: Diagnosis

Condition

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7 conditions tested. Click Indication tab for more information.

Methodology

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Molecular Genetics
DDeletion/duplication analysis
Next-Generation (NGS)/Massively parallel sequencing (MPS)
  • Illumina MiSeq
CSequence analysis of the entire coding region
Next-Generation (NGS)/Massively parallel sequencing (MPS)
  • Illumina MiSeq

Summary of what is tested

47 genes and variants. Click Methodology tab for more information.

Genes

Clinical validity

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Not provided

Clinical utility

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Not provided

Testing strategy

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Next Generation Sequencing of 43 genes. Low-coverage regions (<30 reads) are analysed by Sanger Sequencing. CNV analysis is performed on the NGS data.

How to order

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Using our website
Order URL Help: https://genomediagnostics.amsterdamumc.nl/information-and-order/catalog/home.html?q=NGS+panel+-+Arrhythmia

Suggested reading

  • HRS/EHRA/APHRS, 2013
    Executive summary: HRS/EHRA/APHRS expert consensus statement on the diagnosis and management of patients with inherited primary arrhythmia syndromes.

Practice guidelines

  • AHRQ, 2013
    Assessment on Implantable Defibrillators and the Evidence for Primary Prevention of Sudden Cardiac Death

Consumer resources

IMPORTANT NOTE: NIH does not independently verify information submitted to the GTR; it relies on submitters to provide information that is accurate and not misleading. NIH makes no endorsements of tests or laboratories listed in the GTR. GTR is not a substitute for medical advice. Patients and consumers with specific questions about a genetic test should contact a health care provider or a genetics professional.

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