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AmpliSeq for Illumina

AmpliSeq for Illumina Neurological Research Panel

This sequencing research panel assesses 751 genes known to harbor variants affecting brain and nervous system function.

Overview

This research panel assesses 751 genes known to harbor variants affecting the functioning of the brain and nervous system. In addition to targeting all coding regions, an additional 101 non-coding disease-causing loci are targeted, as well as 14 repeat-expansion regions in genes AFF2, AR, ATN1, ATXN7, ATXN8OS, ATXN3, CACNA1A, CSTB, DMPK, HTT, JPH3, PABPN1, PPP2R2B, and TBP.

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 18077 total. 2 pools. (Pool 1: 9045 amplicons. Pool 2: 9032 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™ Neurological Research Panel for Illumina®

20020497

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

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