AmpliSeq for Illumina Hearing Loss Research Panel v1

This sequencing research panel assesses 63 genes known to harbor variants associated with hearing loss. Read More...
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AmpliSeq™ Hearing Loss Research Panel v1 for Illumina®



Product Highlights

This research panel was developed as a quick, accurate, and cost-effective method to identify genetic mutations associated with hearing loss. The panel assesses hearing function-related variants in 63 genes.

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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