Description
Overview
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
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.
Example workflow
AmpliSeq for Illumina Myeloid Panel
AmpliSeq for Illumina Library PLUS
AmpliSeq for Illumina CD Indexes
MiniSeq System
MiSeq System
NextSeq System
BaseSpace Sequence Hub DNA Amplicon App
BaseSpace Sequence Hub RNA Amplicon App
Local Run Manager RNA and RNA Modules
