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DNBSEQ-G50 Genetic Sequencer

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The DNBSEQ-G50 is a compact benchtop genetic sequencer. Thanks to its design featuring two different flow-through cuvettes, it offers flexibility and strikes the perfect balance between speed and affordability. The FCS (small flow cell) enables short run times for time-sensitive...

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The DNBSEQ-G50 is a compact benchtop genetic sequencer. Thanks to its design featuring two different flow-through cuvettes, it offers flexibility and strikes the perfect balance between speed and affordability. The FCS (small flow cell) enables short run times for time-sensitive (STAT) samples, while the FCL (large flow cell) offers a lower cost per sample. The DNBSEQ-G50 offers read length options of 3–5 for both the FCS and FCL, supporting a wide range of research and clinical applications, such as low-coverage whole-genome sequencing, targeted sequencing, small-scale whole-genome sequencing, RNA sequencing, and whole-exome sequencing, among others.

Key Benefits

  1. Compactness and flexibility: The DNBSEQ-G50 is a next-generation benchtop sequencer that takes up minimal space while maintaining high throughput.
  2. High accuracy: DNBSEQ™ technology reduces error rates, index jumps, and duplicates.
  3. Automated end-to-end workflow: From library preparation to bioinformatics analysis—everything is integrated into a single, user-friendly system.
  4. Wide compatibility: supports most commercial library preparation kits and analysis software.
Technical Specifications 
Flow-through cuvette type Number of reads Read length Data output Run time Q30
FCS 100M 100M 75–100M SE100 PE100 PE150 ~10G ~20G 23–30G ~10 hrs ~20 hrs ~28 hrs >80% >85% >80%
FCL 500M 500M 500M 500M 500M SE50 PE50 SE100 PE100 PE150 ~25G ~50G ~50G ~100G ~150G ~7 hrs ~15 hrs ~13 hrs ~26 hrs ~40 hrs >85% >85% >85% >85% >80%
 

Applications

  • Genomics: low-coverage and whole-genome sequencing of humans and microorganisms.
  • Medical diagnostics: panels for oncological and hereditary diseases.
  • Transcriptomics: RNA sequencing, including expression and epigenetic analysis.
  • Cell engineering: verification of the effectiveness of CRISPR genome editing
  • Epidemiology and microbiology: pathogen identification, tracking viral evolution.

Why choose the DNBSEQ-G50?

  • Reliability and reproducibility: stable results with low coefficient of variation even on complex samples.
  • Quick setup and ease of use: a simple interface and automation reduce manual labor.
  • High efficiency in mutation detection: ensures accurate detection of even rare genomic variations.

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