AmpliSeq for Illumina Deafness Research Panel v2

This sequencing research panel targets genetic variants associated with inherited deafness. The panel assesses 126 hearing function-related genes. Read More...
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AmpliSeq™ Deafness Research Panel v2 for Illumina®



Product Highlights

This panel provides a quick, accurate, and cost-effective way for researchers to identify genetic variants associated with inherited deafness. This panel was designed based on extensive curation of peer-reviewed literature, disease research databases, and consultation with key opinion leaders. The panel assesses 126 genes known to harbor variants affecting hearing function.

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.

Other Required Products

In addition to the community panel, you will also need an AmpliSeq Library PLUS kit and index adapters.

Additional Information

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