OncoDNA: All-in-one solution with the largest panel in the market
OncoDEEP® Kit DNA & RNA panel is the largest and the most complete of the market. This panel is composed of probes targeting 638 genes for a final content of 1.8 Mb. It supports identification of all relevant variants involved in various solid tumor types with genes carefully selected based on their biological and therapeutical relevance.
Clinically-relevant oncology targets and biomarkers
Designed by oncology experts, the OncoDEEP® panel contains the most relevant and complete cancer gene panel. Over the time this panel was optimized to include all clinically-relevant oncology targets. The panel is composed of 638 genes, reporting genomic alterations (SNV, insertion, deletion, CNV) and complex genetic signature (HRD, MSI and TMB).
From sample preparation to clinical insights in just 5 days!
Paragon Genomics: Targeted NGS amplicon Panels to fit your research and diagnostic needs
FOR EVERY APPLICATION: Tumor Profiling, Immuno-oncology, Cancer Liquid Biopsy, Inherited Diseases, Pharmacogenomics, Gene editing / CRISPR QC, Agrigenomics / Genotyping by Sequencing (GBS), Metagenomics.
CleanPlex® NGS panels are powered by Paragon Genomics’ CleanPlex Technology, which uses a proprietary multiplex PCR background cleaning chemistry to effectively remove non-specific PCR products, resulting in optimized, best-in-class target enrichment performance and efficient use of sequencing reads. → Save on sequencing costs
Low-input, fast 3h workflow and high performance NGS panels to target up to >20,000 amplicons in a single tube reaction. Available as catalog products and cost-efficient CUSTOM solutions. Especially suitable for clinical and translational research.
MULTIPLEX-PCR-BASED AMPLICON PANELS:
- Easy & fast (3h) single-tube workflow
- Input DNA as low as 0.1 – 10 ng
- Designed for germline & somatic variant detection, sensitivity down to 1% allele frequency (UMI –panels 0.1 %)
- 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.
- Sample Types: genomic DNA, FFPE, circulating cell-free DNA (cfDNA), fresh and frozen tissue
- Provides high on-target percentage and coverage uniformity >95%
- Compatible with Illumina, Ion Torrent and MGI platforms.
Available as CUSTOM – Ask for a free design quote to define Your Targets! Edit the catalog panels or design your own. Multiplex up to 20 000+ amplicons in each reaction. ALL-INCLUSIVE COST-EFFICIENT SOLUTION offering PCR primer pairs, lib prep reagents, unique dual indexed sequencing adapters and magnetic purification beads all in a single kit.
CATALOG PRODUCTS:
- CleanPlex® TMB 500 Panel
- CleanPlex® OncoZoom® Cancer Hotspot Panel
- CleanPlex® TP53 Panel
- CleanPlex® UMI Lung Cancer Panel
- OmniFusion™ RNA Lung Cancer Panel (To detect unknown fusions)
- AccuFusion™ RNA Lung Cancer Panel (To detect known fusions)
- CleanPlex® BRCA1 & BRCA2 Panel v3
- CleanPlex® Hereditary Cancer Panel v2 (to target 37 genes)
- CleanPlex® Mitochondrial Disease Panel
- CleanPlex® CFTR Panel
Daicel Arbor Biosciences: Hybridization capture panels for targeted sequencing
myBaits target capture kits are compatible with any sequencing platform and with these in-solution biotinylated RNA probes you can target any region in a genome
Predesigned panels:
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myBaits Custom:
Design your own custom enrichment panels for your DNA/RNA/Methyl-Seq project with the assistance of Arbor’s team of expert scientists.
Make your workflow seamless with the NEW Library Preparation Kits for myBaits® – Read more
