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NGS Panels and DNAseq

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 therapeutic 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

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BioVendor: fastGEN

Breakthrough fast system for one-step NGS library

BioVendor brings new technology fastGEN for examination of the mutation status of oncomarkers in samples. Technology is based on ultra-deep sequencing of short amplicons obtained by a single polymerase chain reaction with special tagged hybrid primers. It’s simple, ultra-sensitive, specific and effective – it is perfectly adapted to diagnostics and offers new advantages for clinical material.

Fast – Simple – Reliable – Robust

Diagnostic kits with software solution for KRAS, NRAS, BRAF, EGFR, IDH 1/2, CFTR, POLE/CTNNB1, PIK3CA, TERT and TP53 genes with excellent analytical parameters and extremely fast processing. And the latest kit BCR::ABL Cancer Kit.

GENOVESA software fastGEN module is a cloud all-in-one solution for the analysis of raw data (FASTQ files) with technical and application support.

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Daicel Arbor Biosciences:

Robust NGS library preparation for targeted sequencing

Make your workflow seamless with the new Library Preparation Kits for myBaits®. This new DNA library prep kit uses enzymatic fragmentation to generate high-complexity libraries ready for hybridization capture. Compatible even with degraded samples, it is the perfect companion to any myBaits® project.

Get better data – faster – with the new Library Prep Kit for myBaits targeted sequencing. Libraries built with this kit can be paired with any appropriate myBaits Custom or Predesigned kit. Read more

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 for microbes & viruses, plants, human, animals.

Also myBaits Custom Panels! Design your own custom enrichment panels for your DNA/RNA/Methyl-Seq project with the assistance of Arbor’s team of expert scientists.

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Paragon Genomics:

Targeted NGS amplicon Panels to fit your research and diagnostic needs

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.

 

LGC Biosearch: DNAseq kits

Challenging, degraded samples, FFPE, cfDNA and low input samples

NxSeq UltraLow DNA Library Kit v2: Cost effective library preparation with high efficiency adaptor ligation to produce complex and uniform libraries from 50 pg to 100 ng of sheared DNA. Quick 3 hour protocol. Kits in 12 or 96 rxns. Pair with NxSeq Single or Dual Indexing kits.

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Liisa Peri

Product Manager, Life Science and NGS, Marketing Manager +358 41 502 3646