BioVendor: fastGEN – Breakthrough fast system for one-step NGS library
Fast – Simple – Reliable – Robust
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.
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.
Daicel Arbor Biosciences: Robust NGS library preparation for targeted sequencing
Make your workflow seamless with the new Library Preparation Kits for myBaits®
Daicel Arbor Biosciences’s 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
- Premium formulas – Advanced enzyme mixes make the most of even low-input or degraded DNA samples.
- Convenient kits – Unique sizes provide maximum compatibility with myBaits capture.
- Full workflow – A complete targeted sequencing solution when paired with your myBaits kit and preferred barcoding system.
- Broad compatibility – Prep 1-500 ng high molecular weight or degraded dsDNA.
Libraries built with this kit can be paired with any appropriate myBaits Custom or Predesigned kit.
LGC Biosearch: 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.
