AmpliSeq for Illumina Childhood Cancer Panel
Targeted panel for investigating 203 genes associated with cancer in children and young adults.
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Product Highlights
The AmpliSeq Childhood Cancer Panel for Illumina provides a targeted resequencing solution for comprehensive evaluation of somatic variants associated with childhood and young adult cancers.
Key features include:
- Comprehensive Gene Content
Target multiple variant types across 203 genes, including hotspots, single nucleotide variants (SNVs), indels, copy number variants (CNVs), and gene fusions - Fast, Streamlined Workflow
Prepare sequencing libraries in a single day with as little as 10 ng high-quality DNA or RNA from blood, bone marrow, or formalin-fixed, paraffin-embedded (FFPE) samples - Accurate Data
Detect somatic mutations down to 5% frequency using local or cloud-based analysis
The AmpliSeq Childhood Cancer Panel for Illumina is part of an integrated workflow that includes AmpliSeq for Illumina polymerase chain reaction (PCR)-based library preparation, Illumina sequencing by synthesis (SBS) next-generation sequencing (NGS) technology, and automated analysis
This ready-to-use panel detects variants within multiple pediatric cancer types, including leukemias, brain tumors, and sarcomas while saving time and efforts associated with identifying targets, designing primers, and optimizing panels.
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Product Literature
Automated Solutions for AmpliSeq for Illumina Sequencing Panels
Application note | HTML
AmpliSeq for Illumina Childhood Cancer Panel Data Sheet
Data sheet | HTML
AmpliSeq for Illumina Childhood Cancer Panel Gene List
product_file | EXCEL < 1 MB
Application note | PDF | 5 versions
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