AmpliSeq for Illumina Hematology Research Panel

This sequencing research panel assesses 394 genes known to harbor variants associated with inherited hematological disorders.Read More...
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AmpliSeq™ Hematology Research Panel for Illumina®

20020497

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Product Highlights

This Mendelian Disease (single gene disorders) research panel was developed as a quick, accurate, and cost-effective method to identify genetic variants associated with inherited hematological disorders. The panel assesses 394 genes known to harbor mutations affecting the blood. In addition to targeting all coding regions, an additional 161 non-coding disease-causing loci are targeted.

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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