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AmpliSeq for Illumina

AmpliSeq for Illumina Dementia Research Gene Panel

This sequencing research panel was developed to help identify genetic variants associated with early onset dementia.

Overview

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.

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.

Learn more about DesignStudio

Additional information

Learn more about Ampliseq for Illumina

Specifications

Input quantity 1–100 ng; recommended 10 ng per pool
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

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

/ Results

Documentation

Product literature
Support documentation

Panel (1)

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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