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.


Specifications


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

of

Panel (1)

AmpliSeq™ Cardiovascular Research Panel for Illumina®

20020497

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

Sign in to add to cart or see pricing.

List Price:

Discounts:

Showing of

Selection summary

Product

Qty

Unit Price

Frequently purchased

Order the NovaSeq X Series

Advanced chemistry, optics, and informatics combine to deliver exceptional speed and data quality, outstanding throughput and scalability.

MiSeq Reagent Kit v3

Optimized reagent kit that provides increased cluster density and read length, improving sequencing quality scores compared to earlier versions.

TruSight Oncology 500

Enable CGP with a large pan-cancer panel covering all major variant classes plus gene signatures (TMB, MSI, and HRD) from FFPE tissue.

Illumina DNA Prep

A fast, integrated workflow for preparing libraries for use in a wide range of sequencing applications.

Speak with a specialist

Reach out for information about our products and services, or get answers to questions about our technology.