Optimized for all Illumina® sequencing platforms
Inputs as low as 10 ng
Designed for germline and somatic variant detection
Offers overlapping amplicons in a fast, easy single-tube workflow
Provides high on-target percentage and coverage uniformity, enabling low frequency (> 1%) variant discovery and confirmation
Pre-Designed NGS Panels
- Accel-Amplicon 56G Oncology Panel v2
- Accel-Amplicon Plus 57G Pan-Cancer Profiling Panel
- Accel-Amplicon Comprehensive TP53 Panel
- Accel-Amplicon EGFR Pathway Panel
- Accel-Amplicon BRCA1 and BRCA2 Panel
- Accel-Amplicon BRCA1, BRCA2, and PALB2 Panel
- Accel-Amplicon Plus Colorectal (CRC) Cancer Panel
- Accel-Amplicon Plus Lynch Syndrome Panel
- Accel-Amplicon Plus Lung Cancer Panel
- Accel-Amplicon Plus Myeloid Panel
- Accel-Amplicon CFTR Panel
- Accel-Amplicon Sample_ID Panel