Do you want to detect and sequence specific genes, variants or gene fusions?
Custom NGS Amplicon Panels from Paragon Genomics. Just create the list of your targets of interest, and we’ll do the rest!
Within 4-6 weeks, you’ll receive all reagents needed for targeted multiplex-PCR based amplicon sequencing. Prepare the libraries by yourself or ask service from a core lab!
Key features:
- Flexibility for content, sample type and ANY species – Applications page
- Include up to 30,000 amplicons per single tube
- Sensitivity: detect mutations down to 1% allele frequency (UMI panels 0.5%)
- Specificity: High on-target rate and coverage uniformity >95%
- Detection of and analysis for single nucleotide variants (SNVs), small insertions and deletions (Indels), copy number variations (CNVs), gene fusions / splice variants, gene expression level, tumor mutational burden (TMB), microsatellite instability (MSI), internal tandem duplication (ITD), etc.
- gDNA, RNA, FFPE and cfDNA compatible designs
- Short protocol 3-6h, depending on the approach/panel type
- High-level sample multiplexing with 384plex UDIs or 2688plex CDIs, on Illumina platforms
- Save on sequencing cost and skip the intensive PCR optimization!
- Check the publication list here
Options available:
- CleanPlex Custom amplicon panels – For every sample type & organism
- CleanPlex Custom panels with UMIs – For low input DNA, cell-free DNA, liquid biopsies
- CleanPlex Custom RNA Fusion panels – Detect known or unknown gene fusions
More than 500 Custom Panels have been designed! Ask for a quote for your custom project, or check the catalog listing here.
