AmpliSeq for Illumina Comprehensive Cancer Panel

Targeted panel investigating the exonic regions of 409 genes with known associations to cancer.Read More...
What products do I need?

AmpliSeq™ Comprehensive Cancer Panel for Illumina®


Library Prep

AmpliSeq™ Library PLUS (24 Reactions) for Illumina®


AmpliSeq™ Library PLUS (96 Reactions) for Illumina®


AmpliSeq™ Library PLUS (384 Reactions) for Illumina®


Index Adapters

AmpliSeq™ CD Indexes Set A for Illumina® (96 Indexes, 96 Samples)



AmpliSeq™ for Illumina® Sample ID Panel


AmpliSeq™ for Illumina® Direct FFPE DNA


AmpliSeq™ Library Equalizer for Illumina®


Product Highlights

The AmpliSeq for Illumina Comprehensive Cancer Panel provides a targeted resequencing solution for analyzing somatic mutations across 409 genes with known associations to cancer. Key features include:

Relevant Gene Content
  • Target all-exon coverage of 409 cancer-associated genes
Fast, Streamlined Workflow
  • Prepare sequencing-ready libraries in a single day from as little as 1 ng of high quality or 10 ng of formalin-fixed, paraffin-embedded (FFPE) input samples
Accurate Data
  • Detect somatic mutations below 5% frequency using local or cloud analysis

The Comprehensive Cancer Panel 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 panel detects variants within multiple cancer types, including lung, colon, breast, ovarian, melanoma prostate, and hematologic malignancies. The ready-to-use panel saves you the time and effort of identifying targets, designing primers, and optimizing panels.

Learn More About AmpliSeq for Illumina

Frequently Purchased Together



仪器 推荐的样本数 读长
NextSeq 550 System 每次运行的样本:中通量:4,高通量:12(假设最小覆盖度为500倍) 2 × 150 bp


AmpliSeq for Illumina Comprehensive Cancer Panel AmpliSeq for Illumina Cancer Hotspot Panel v2
内容说明书 409个癌症相关基因的全外显子覆盖。 50种与癌症具有已知关联的基因的热点区域
变异种类 拷贝数变异(CNV), 单核苷酸多态性(SNP), 体细胞变异, 插入缺失 插入缺失, 体细胞变异, 单核苷酸多态性(SNP)
多重分析 96个双索引组合 96个双索引组合
技术 测序 测序
方法 靶向DNA测序 , 扩增子测序 靶向DNA测序 , 扩增子测序
核酸类型 DNA DNA
物种类别 人类 人类
特殊的样本类型 血液, FFPE组织 血液, FFPE组织
癌症类型 泛癌, 实体瘤 泛癌, 实体瘤
系统兼容性 NextSeq 550 研究模式下的MiSeqDx , iSeq 100 , MiniSeq , MiSeq , MiSeq
起始量 1–100 ng(建议每个混池10 ng) 1–100 ng(建议每个混池10 ng)

Method-Specific Workflow Example


Related Products

TruSight Oncology 500

Assay targeting multiple variant types, including tumor mutational burden (TMB) and microsatellite instability (MSI), even from low-quality samples.

AmpliSeq for Illumina Comprehensive Panel v3

Targeted DNA and RNA research panel investigating variants across 161 genes associated with a range of cancer types.

AmpliSeq for Illumina Custom DNA Panel

Targeted custom research panels optimized for sequencing specific targets or genomic content of interest.