AmpliSeq for Illumina Exome Panel

Targeted research panel for sequencing the protein-coding regions of the human genome.Read More...
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Panel

AmpliSeq™ Exome Panel for Illumina®

20019166


Library Prep

AmpliSeq™ Library PLUS (24 Reactions) for Illumina®

20019101

AmpliSeq™ Library PLUS (96 Reactions) for Illumina®

20019102

AmpliSeq™ Library PLUS (384 Reactions) for Illumina®

20019103


Index Adapters

Ampliseq™ CD Indexes Large Volume for Illumina® (96 Indexes, 96 Samples)

20019108

配件产品

AmpliSeq™ for Illumina® Sample ID Panel

20019162

AmpliSeq™ for Illumina® Direct FFPE DNA

20023378

AmpliSeq™ Library Equalizer for Illumina®

20019171

产品特色

The AmpliSeq for Illumina Exome Panel brings the speed and simplicity of PCR to exome sequencing, enabling researchers to sequence eight exomes in a single run and identify germline variants in less time. Key features include:

Fast exome library preparation
  • Prepare 8 exome libraries in < 7.5 hours with < 1.5 hours hands-on time
Comprehensive coverage
  • Access uniform and specific coverage; includes >97% of the Consensus Coding Sequences (CCDS) annotation
Accurate Data
  • Detect common single nucleotide variants (SNVs), copy number variants (CNVs), and small indels

The Exome 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 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

规格

计划推荐

仪器 推荐的样本数 读长
NextSeq 550 System 每次运行的样本:高通量:每次运行8个样本(基于95%以上的覆盖度为30倍) 2 x 151 bp

产品比较

Method-Specific Workflow Example

 

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