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.Read More...
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AmpliSeq™ Cardiovascular Research Panel for Illumina®

20020497

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Product Highlights

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.

Other Required Products

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

Additional Information

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Specifications