fastGEN® — One-step NGS library prep for oncology
Significantly reduce hands-on time with a fast, amplicon-based workflow that processes multiple targets in parallel.
Why fastGen:
- Unique
Simple. Ultra-sensitive, specific, and effective technology - Fast
Excellent speed, <30 min hands-on - Reliable
Uniform coverage for different amplicons and different samples - Robust
Using short amplicons obtained by a single polymerase chain reaction with special tagged hybrid primers
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Product overview
A breakthrough system for one-step NGS library
preparation, panels for quick and easy detection
of clinically relevant oncomarkers.
- One-step NGS library prep: fast, user-friendly, amplicon workflow for targeted mutation detection.
- Parallel processing of genes/samples: designed to run selected genes together for efficient throughput.
- Panel choice & regulation: Smart portfolio with clinically relevant oncomarkers.
- Click-and-analyze in GENOVESA: cloud module accepts FASTQ from Illumina; conversion kit available for other platforms.
fastGEN – Next Generation Sequencing 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.
fastGEN kits
BioVendor’s NGS portfolio is designed to meet the diverse needs of modern laboratories, offering a comprehensive solution built on three key pillars: fastGEN, epicGEN, and the bioinformatics software GENOVESA.
| Product | Gene | Detail | Sequencer compatiblity | Regulatory status |
|---|---|---|---|---|
| fastGEN Solid cancer kit |
NRAS KRAS BRAF |
for rapid preparation of the sequencing library for genotyping the KRAS, NRAS (codons 12, 13, 59, 60, 61, 117, and 146) and BRAF (codons 600 and 601) genes |
Illumina MiSeq | CE-IVD |
| fastGEN Lung cancer kit |
EGFR | for rapid preparation of the sequencing library for genotyping the EGFR gene (exons 18, 19, 20, and 21) | Illumina MiSeq | CE-IVD |
| fastGEN Brain cancer kit |
IDH1 IDH2 |
for rapid preparation of the sequencing library for genotyping the IDH1 and IDH2 genes (codons 132 and 172). | Illumina MiSeq | CE-IVD |
| fastGEN BCR::ABL1 Cancer Kit |
BCR::ABL1 fusion gene | The kit covers codons 237-510. Major, minor and micro breakpoint cluster regions included |
All Illumina platforms & GeneMind, MGI AVITI |
RUO |
| fastGEN POLE/CTNNB1 kit* |
POLE CTNNB1 |
for rapid preparation of the sequencing library for genotyping the POLE gene (codons 286, 411, 297, 459, 456, 367, 424, 295, 436, 444, and 368) and CTNNB1 (codons 22-62, 318-344, 371-395) | All Illumina platforms & GeneMind, MGI AVITI |
RUO |
| fastGEN TP53 kit* |
TP53 | for rapid preparation of the sequencing library for genotyping the TP53 gene (exons 2-11, 2 non-canonical exons between exons 9 and 10, and adjacent introns) | All Illumina platforms & GeneMind, MGI AVITI |
RUO |
| fastGEN PIK3CA kit* |
PIK3CA | for rapid preparation of the sequencing library for genotyping the PIK3CA gene (exact codons in exons 2, 3, 5, 7, 8, 10, 14 and 21) | All Illumina platforms & GeneMind, MGI AVITI |
RUO |
| fastGEN Solid cancer kit II* |
NRAS KRAS BRAF |
for rapid preparation of the sequencing library for genotyping the KRAS, NRAS (codons 12, 13, 59, 60, 61, 117, and 146) and BRAF (codons 600 and 601) gene | All Illumina platforms & GeneMind, MGI AVITI |
RUO |
*Does not contain R1SP.
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