Order the NovaSeq X Series
Advanced chemistry, optics, and informatics combine to deliver exceptional speed and data quality, outstanding throughput and scalability.
This sequencing research panel was developed to help identify genetic variants associated with early onset dementia.
This panel was developed as a quick, accurate, and cost-effective research method to identify genetic variants associated with early onset dementia. The panel assesses 17 genes known to harbor variants linked to dementia (PRNP, PSEN1, PSEN2, APP, GRN, MAPT, TREM2, CHMP2B, CSF1R, FUS, ITM2B, NOTCH3, SERPINI1, TARDBP, TYROBP, VCP, and SQSTM1). This panel contains 214 amplicons in 2 pools.
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; recommended 10 ng per pool |
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Method | Amplicon sequencing |
Nucleic acid type | DNA |
Number of amplicons | 214 total. 2 pools. (Pool 1: 109 amplicons. Pool 2: 105 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™ Dementia Research Gene Panel for Illumina®
20020495
Custom assay supporting 750 or 3000 samples with < 4999 amplicons. Purchase Library PLUS and index adapters separately.
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