Order the NovaSeq X Series
Advanced chemistry, optics, and informatics combine to deliver exceptional speed and data quality, outstanding throughput and scalability.
This sequencing research panel assesses 394 genes known to harbor variants associated with inherited hematological disorders.
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.
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.
Input quantity | 1–100 ng (10 ng recommended per pool) |
---|---|
Method | Amplicon sequencing |
Nucleic acid type | DNA |
Number of amplicons | 7434 total. 2 pools. (Pool 1: 3722 amplicons. Pool 2: 3712 amplicons). |
Species category | Human |
Technology | Sequencing |
In addition to the community panel, you will also need an AmpliSeq Library PLUS kit and index adapters.
AmpliSeq™ Hematology Research Panel for Illumina®
20020497
Sufficient for 3000 samples with > 4999 amplicons. Purchase Library PLUS and index adapters separately.
List Price:
Discounts:
Showing of
Product
Qty
Unit Price
Product
Catalog ID
Quantity
Unit price
Reach out for information about our products and services, or get answers to questions about our technology.
Your email address is never shared with third parties.