20028446, AmpliSeq™ for Illumina® Childhood Cancer Panel

Name: AmpliSeq™ for Illumina® Childhood Cancer Panel
Brand: Illumina
SKU: 20028446

Targeted panel for assessing somatic variants associated with childhood and young adult cancers. Sufficient for 24 samples. Library Prep reagents, index adapters and accessory products are sold separately.

Catalog Number: 20028446

Pricing

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Category

NGS Library Preparation Kits

TagsSequencing kits Library preparation kits

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

Specifications

General

Assay time	5-6 hr (library prep only; doesn't include library quantification, normalization, or pooling time)
Hands-on time	< 1.5 hr
Input quantity	10 ng high-quality DNA or RNA
Automation capability	Liquid handling robot(s)
Instruments	MiSeq System , NextSeq 550 System , NextSeq 2000 System , NextSeq 1000 System , MiSeqDx in Research Mode , MiniSeq System
Method	Amplicon sequencing
Nucleic acid type	DNA, RNA
Number of reactions	24 reactions
Specialized sample types	Blood, Low-input samples, Bone marrow, FFPE tissue
Species category	Human
Technology	Sequencing
Variant class	Single nucleotide polymorphisms (SNPs), Gene fusions, Somatic variants, Insertions-deletions (indels), Copy number variants (CNVs)

Ordering

Notice

Unless otherwise stated, the minimum order amount is USD 1,000.
For orders below USD 1,000, an additional handling fee may apply, or we may arrange local delivery / local handover where available.
All quotations are subject to final confirmation, including product availability, lead time, batch information, shipping cost, and applicable export or handling requirements.
For quotation requests, please send an RFQ from website or contact:

[email protected]

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