Accel-Amplicon NGS Panels utilize multiple overlapping amplicons in a single tube, using a rapid, 2-hour workflow to prepare ready-to-sequence libraries. Primer pairs in Accel-Amplicon NGS Panels are compatible with short DNA fragments and are designed for generating libraries from input DNA as low as 10 ng. This unique design enables applications utilizing limiting or damaged samples such as FFPE and cfDNA, and provides powerful solutions for detecting variants and screening clinically-relevant mutations with limit of detection down to 1%.
Key benefits include:
Optimized for all Illumina® sequencing platforms
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
The Accel-Amplicon NGS Panels are available in two formats:
Accel-Amplicon Pre-Designed NGS Panels — Expertly designed panels using content from peer-reviewed publications and thought leader input. Includes assays for cancer genes, rare disease, and sample tracking.
Accel-Amplicon Custom NGS Panels — Start from scratch. We’ll help you through the design process and validate a unique panel for you to cover exactly what you need.
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 Sample_ID Panel
Accel-Amplicon Custom NGS Panels
