Next Generation Sequencing (NGS)

fastGEN kits

Meet the fastGEN technology

BioVendor brings new technology fastGEN for examination of the mutation status of markers in samples. Technology is based on ultra-deep sequencing of short amplicons obtained by a single polymerase chain reaction with special tagged hybrid primers.

The fastGEN technology is simple, ultra-sensitive, specific and effective - it is perfectly adapted to diagnostics and offers new advantages for clinical material.

We developed NGS kits to analyse selected genes.
Our fastGEN technology is designed to allow parallel processing of samples for all selected genes.

User-friendly NGS kits

BioVendor developed user friendly diagnostic NGS kits with excellent analytical parameters and extremely fast processing for laboratories of any size.
The kit contains ready-to-use Master Mixes with sample indexes, read1 (applies to selected kits only), read2 seq primers and an index seq primer.

See fastGEN portfolio

Four reasons why fastGEN is worth your attention

• Unique

  Simple, ultra-sensitive, specific, and effective technology

• Fast

  Excellent speed (<30 min hands-on time)

• Reliable

  Significantly lower probability of mistakes, uniform coverage for different amplicons and different samples

• Robust

  Robustness achieved by using short amplicons obtained by a single polymerase chain reaction with special tagged hybrid primers

It’s faster. Way faster!

epicGEN kits

epicGEN introduces a next-generation technology for precise examination of mutation status in target biomarkers. The technology is based on ultra-deep sequencing of selectively enriched genomic regions, utilizing an optimized hybrid capture system for maximum specificity and sensitivity.

The epicGEN technology is highly precise, ultra-sensitive, specific, and efficient – perfectly suited for clinical diagnostics and translational research, offering new advantages for analyzing complex genetic variations.

New generation of NGS panels

Our epicGEN technology is designed to enable high-efficiency hybrid capture, allowing parallel processing of samples for all targeted genes with maximum specificity and uniform coverage.
epicGEN delivers user-friendly diagnostic NGS kits with exceptional analytical performance and optimized hybrid capture technology, ensuring high precision and efficiency for laboratories of any size.

See epicGEN portfolio 

Five reasons why epicGEN stands out

• Specific

  Highly specific oligonucleotides precisely target desired sequences, minimizing non-specific enrichment and improving coverage.

• Uniform

  Optimized design ensures consistent coverage across target regions, maximizing sequencing efficiency and reliability.

• Accurate

  Minimizes off-target binding, reducing interference from non-coding and repetitive genomic regions for greater precision.

• Sensitive

  Enables reliable enrichment from just less than 1ng of DNA, supporting analysis of challenging samples like cfDNA, FFPE tissues, and rare biological materials.

• Powerful

  Detects somatic mutations at VAF >1% with sufficient sequencing depth (~500×), ensuring high sensitivity in mutation analysis.

Software

The analysis of genetic NGS data can be a daunting task that often requires specialized computing skills by the user.
We have developed our proprietary web-based bioinformatic analysis software – GENOVESA as an effortless solution for everyone and for all NGS data regardless of the kit used. 

GENOVESA  - Bioinformatic analysis software

GENOVESA is intuitive and easy to use. For beginners in NGS analysis, it allows a quick and easy generation of relevant information of their NGS data, without the need of their own dedicated bioinformatic experts. 

On the other hand, GENOVESA allows experienced users to adjust and modify parameters, use complex filtering rules, and visually evaluate variants at the individual reading level.  

Key features

• Advanced quality control of sequencing data
• Automatic notification of low-coverage regions for simple filtering of relevant variants
• Monthly update of annotation databases
• Customisation
• Patient data and variants stored in an internal database
• One-click report
  
  

Visit software GENOVESA 

Clinical topics

NGS products cover the most common branches of clinical diagnostics.

Oncology

Cystic fibrosis

Food intolerance

Documents

Documents for partners, distributors and end customers.

• Instructions for Use

  fastGEN BCR::ABL1 Cancer Kit
  fastGEN Brain Cancer Kit
  fastGEN CFTR 24-kit
  fastGEN CFTR 8-kit
  fastGEN H3F3A/IDH1/2 Cancer Kit
  fastGEN Intolerance Kit I
  fastGEN Lung Cancer Kit
  fastGEN MSI Kit
  fastGEN PIK3CA Cancer Kit
  fastGEN POLE/CTNNB1 Cancer Kit
  fastGEN Solid Cancer Kit
  fastGEN Solid Cancer Kit II
  fastGEN TERT Cancer Kit
  fastGEN TP53 Cancer Kit
  fastGEN TP53 Cancer 32-kit
  

• Marketing Documents

  epicGEN Solid Cancer & MSI Kit leaflet
  fastGEN leaflet
  fastGEN leaflet-short version
  CFTR leaflet
  fastGEN Intolerance Kit I leaflet
  fastGEN MSI Kit leaflet
  GENOVESA leaflet
  Hemato-oncology leaflet

Please note
Specific product documentation you can find on the product detail webpage.

Are you interested in more? Contact our product manager.

Iveta Tóthová, PhD.