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AmpliSeq for Illumina

AmpliSeq for Illumina Cardiovascular Research Panel

This sequencing research panel identifies genetic variants linked to inherited cardiovascular defects. It assesses 404 cardiovascular function-related genes.

Overview

This Mendelian Disease (single gene disorders) panel was developed as a quick, accurate, and cost-effective research method to identify genetic variants associated with inherited cardiovascular defects. The panel assesses 404 genes known to harbor variants affecting cardiovascular functioning. In addition to targeting all coding regions, an additional 94 non-coding disease-associated loci are targeted, as well as special coverage of two repeat expansion regions in genes DMPK and CACNA1A.

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 10430 total. 2 pools. (Pool 1: 5222 amplicons. Pool 2: 5208 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

/ Results

Documentation

Product literature
Support documentation

Panel (1)

AmpliSeq™ Cardiovascular Research Panel for Illumina®

20020497

Sufficient for 3000 samples with > 4999 amplicons. Purchase Library PLUS and index adapters separately.

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