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AmpliSeq for Illumina

AmpliSeq for Illumina Cardiac Arrhythmias and Cardiomyopathy Research Panel

This sequencing research panel targets genetic variants associated with cardiac arrhythmias and cardiomyopathies. It assesses 92 heart function-related genes.

Overview

This research panel provides a quick, accurate, and cost-effective way to study genetic variants associated with cardiac arrhythmias and cardiomyopathies. It assesses 92 genes known to harbor variants affecting heart functioning. It was designed based on extensive curation of peer-reviewed literature, disease research databases, and consultation with key opinion leaders.

Community panel features

AmpliSeq for Illumina Community Panels are made-to-order. We provide the designs for your convenience; however, they do not have associated performance metrics. For predesigned and tested content, view AmpliSeq for Illumina Ready-to-Use Panels.

AmpliSeq for Illumina Community Panels contain content selected and designed with input from leading disease researchers. You can order this community panel as is, or customize the panel to meet your needs, using DesignStudio software to add or remove genes and amplicons.

Learn more about DesignStudio

Additional information

Learn more about AmpliSeq for Illumina

Specifications

Input quantity 1–100 ng; recommended 10 ng per pool
Method Amplicon sequencing
Nucleic acid type DNA
Number of amplicons 2198 total. 2 pools. (Pool 1: 1103 amplicons. Pool 2: 1095 amplicons).
Species category Human
Technology Sequencing

Required products

In addition to the community panel, you will also need an AmpliSeq Library PLUS kit and index adapters.

Order Library PLUS and Adapters

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Documentation

Product literature
Support documentation

Panel (1)

AmpliSeq™ Cardiac Arrhythmias and Cardiomyopathy Research Panel for Illumina®

20020495

Custom assay supporting 750 or 3000 samples with < 4999 amplicons. Purchase Library PLUS and index adapters separately.

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