DNBSEQ-G50: Revolutionizing Genetic Sequencing with Efficiency and Flexibility

Advancements in Life Science Innovation

Focusing on the biotech industry, MGI specializes in R&D, production and sales of equipment and instruments, reagents, and related products to support life science research in a wide range of frontier applications, including precision medicine, precision agriculture, precision healthcare, and more. At MGI, we are working on the improvement of the availability of genomic technologies by providing customers with core tools for life science research and applications.

MGI Patented DNBSEQ™ Technology  – Enhancing Accuracy

DNBSEQ™ provides the advantages of low amplification error rates from DNBs and high-density Patterned Arrays to significantly improve the accuracy of sequencing with a low repetition rate.

Combined with the PCR-free library preparation approach, it reduces the error of entry during amplification and greatly improves the accuracy of detecting SNPs and indels.

The compact and flexible benchtop sequencer  DNBSEQ-G50 empowers flexibility and creates a perfect balance between speed and affordability. Offering different read length options for two different flow cell types, it can support a wide range of research and clinical applications.

Watch the new episode of #MGI Virtual Xpert to learn more about DNBSEQ-G50:

Enhance your daily sequencing capabilities with DNBSEQ-G50

DNBSEQ-G50 is a compact and flexible benchtop genetic sequencer. The design of two different flowcells empowers flexibility and creates a perfect balance between speed and affordability. FCS (Flow Cell Small) allows short turnaround time for short turnaround time (STAT) samples, and FCL (Flow Cell Large) enables lower cost per sample.

DNBSEQ-G50 offers 3-4 read length options for both FCS and FCL, which support a wide range of research and clinical applications such as low-pass whole genome sequencing, targeted sequencing, small whole genome sequencing, RNA sequencing and whole exome sequencing, etc.

• Output:  10~- 150 Gb per run
• Flow cells: 75-100M (FCS), 500M (FCL)
• Read Length: SE50, SE100, PE100, PE150
• Applications: Small whole genome sequencing, targeted DNA/RNA panels, low-pass whole genome sequencing

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