This panel provides a quick, accurate, and cost-effective way for researchers to identify genetic variants associated with inherited dysmorphia-dysplasia disorders. The panel was designed based on extensive curation of peer-reviewed literature, disease research databases, and consultation with key opinion leaders.
AmpliSeq for Illumina Dysmorphia-Dysplasia Research Panel v2
This sequencing research panel assesses 519 genes associated with inherited dysmorphia-dysplasia disorders.
Overview
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.
Additional information
Specifications
| Input quantity | 1–100 ng; recommended 10 ng per pool |
|---|---|
| Method | Amplicon Sequencing |
| Nucleic acid type | DNA |
| Number of amplicons | 12558 total. 2 pools. (Pool 1: 6288 amplicons. Pool 2: 6270 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.
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Documentation
Product literature
Panel (1)
AmpliSeq™ Dysmorphia-Dysplasia Research Panel v2 for Illumina®
20020497
Sufficient for 3000 samples with > 4999 amplicons. Purchase Library PLUS and index adapters separately.
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