The AmpliSeq for Illumina Comprehensive Panel v3 offers coverage of key cancer genes, including kinase domains and genes involved in DNA repair.
The Comprehensive Panel v3 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.
The panel content spans hotspot regions, full-length genes*, copy number genes, and inter- and intragenic gene fusions. This ready-to-use panel saves you the time and effort of identifying targets, designing primers, and optimizing panels.
Instrument | Recommended Number of Samples | Read Length |
---|---|---|
MiniSeq System | 3 samples per run (high output; assumes minimum coverage of 500×) | 2 × 150 bp |
MiSeq System | 3 samples per run with v3 reagents (assumes minimum coverage of 500×) | 2 × 150 bp |
NextSeq 550 System | Samples per run: mid output: 16, high output: 48 (assumes minimum coverage of 500×) | 2 × 150 bp |
AmpliSeq for Illumina Comprehensive Panel v3 | TruSight Tumor 170 | TruSight Tumor 15 | AmpliSeq for Illumina Focus Panel | AmpliSeq for Illumina Cancer Hotspot Panel v2 |
---|
Automated Solutions for AmpliSeq for Illumina Sequencing Panels
Application note | HTML
Data sheet | HTML | 5 versions
Ampliseq for Illumina Comprehensive Panel v3 Gene List
product_file | EXCEL < 1 MB
NextSeq 550 amplicon sequencing solution
Application note | PDF < 1 MB