This sequencing research panel provides a quick, accurate, and cost-effective way to identify genetic variants associated with inherited endocrine disorders.
This research panel assesses 340 genes known to harbor mutations affecting the functions of the endocrine system. This research panel was designed based on extensive curation of peer-reviewed literature, disease research databases, and consultation with key opinion leaders.
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.
| Input quantity | 1–100 ng (10 ng recommended per pool) |
|---|---|
| Method | Amplicon sequencing |
| Nucleic acid type | DNA |
| Number of amplicons | 6359 total. 2 pools. (Pool 1: 3191 amplicons. Pool 2: 3168 amplicons). |
| Species category | Human |
| Technology | Sequencing |
In addition to the community panel, you will also need an AmpliSeq Library PLUS kit and index adapters.
AmpliSeq™ Endocrine Research Panel v2 for Illumina®
20020497
Sufficient for 3000 samples with > 4999 amplicons. Purchase Library PLUS and index adapters separately.
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Advanced chemistry, optics, and informatics combine to deliver exceptional speed and data quality, outstanding throughput and scalability.
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