Accel-Amplicon NGS Panels utilize multiple 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 multiple sequencing platforms
Designed for germline and somatic variant detection
Offers a fast, easy single-tube workflow
Provides high on-target percentage and coverage uniformity, enabling low frequency (> 1%) variant discovery and confirmation
Accel-Amplicon Panels combine the easiest, fastest workflow with flexible content to accelerate your variant discovery and screening. Simply leverage our pre-designed, validated core content or add your own targets. With our fast results and robust on-target performance and coverage uniformity, you’ll have the most informative panel with the best data quality for your scientific needs.
Key features include:
Robust performance on cell-free DNA and FFPE samples starting with as little as 10 ng input.
Highly sensitive detection of rare variants down to 1% allele frequency.
Easy, single-tube assay with sequence ready libraries in 2 hours.
Streamlined analysis with bioinformatics resources such as Primerclip.
Compatible with all Illumina platforms.
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 — Tailor your own assay for the targets most relevant to your needs.
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.
Cancer Gene Profiling
Targeted Sequencing for Cystic Fibrosis
Sample-Tracking
Disease Panels
Microbiome / Metagenomic
Custom NGS Panels
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