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fastGEN – Ultra-fast NGS library prep in one step - Quick and easy tutorial

Experience the simplicity of fastGEN – a breakthrough system for one-step NGS library preparation. This tutorial guides you through the entire workflow, from sample to sequencing-ready library in just 30 minutes of hands-on time.

Built for efficiency, speed, and precision, fastGEN kits are designed to support mutation detection in key oncogenes and tumor suppressor genes. With ready-to-use Master Mixes, indexed primers, and compatibility with GENOVESA for automated data analysis, fastGEN enables confident mutation profiling in both solid and hematological tumors.

Key benefits

  • One-step ultra-deep amplicon sequencing
  • Under 30 min hands-on time
  • Uniform coverage across samples
  • Ultra-sensitive and specific detection
  • Validated for DNA from FFPE, blood (ctDNA), or fresh tissue
  • Seamless data analysis with GENOVESA

Available panels (CE-IVD or RUO):

NRAS, KRAS, BRAF | POLE/CTNNB1 | EGFR | IDH1/IDH2 | PIK3CA | TERT | TP53 | BCR::ABL1 | HER2 | MPN | MSI | and more

Supported by GENOVESA – an automated bioinformatics software for variant annotation, filtering, visualization and clinical reporting.

Find more information about fastGEN kits

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