AmpliSeq for Illumina Exome Panel

AmpliSeq for Illumina Exome Panel

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.

Panel:
20019166 AmpliSeq for Illumina Exome Panel, 24 Reactions
Library Prep:
20019101 AmpliSeq for Illumina Library PLUS, 24 Reactions
20019102 AmpliSeq for Illumina Library PLUS, 96 Reactions
20019103 AmpliSeq for Illumina Library PLUS, 384 Reactions
Indexes:
20019105 AmpliSeq for Illumina CD Indexes Set A, 96 Indexes, 96 Reactions
Project Recommendations
Species Compatibility Human
Recommended Illumina Instrument* NextSeq
Recommended Samples per run† High Output
8
Max Recommended Read Length Up to 2×250
Recommended Secondary Analysis BWA WGS BaseSpace App and ISAAC WGS BaseSpace APP
Recommended Downstream Analysis Variant Interpreter

* Library prep is compatible with all Illumina instruments. Recommended instruments chosen based on typical output and analysis need for selected application.

† >95% covered at 30×

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For Research Use Only

Not for use in diagnostic procedures (except as specifically noted).

Innovative technologies

At Illumina, our goal is to apply innovative technologies to the analysis of genetic variation and function, making studies possible that were not even imaginable just a few years ago. It is mission critical for us to deliver innovative, flexible, and scalable solutions to meet the needs of our customers. As a global company that places high value on collaborative interactions, rapid delivery of solutions, and providing the highest level of quality, we strive to meet this challenge. Illumina innovative sequencing and array technologies are fueling groundbreaking advancements in life science research, translational and consumer genomics, and molecular diagnostics.

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