Illumina Releases Next-Generation Benchtop Sequencers

Illumina Releases Next-Generation Benchtop Sequencers

Highlights
  • Illumina has introduced the MiSeq i100 Series, a benchtop next-generation sequencing system
  • The sequencing system is available in two configurations: the MiSeq i100 and the MiSeq i100 Plus

Illumina, a global leader in DNA sequencing and array-based technologies, has introduced the MiSeq™ i100 Series of sequencing equipment that offers benchtop speed along with simplicity. The MiSeq i100 and MiSeq i100 Plus Systems provide a cost-effective solution for gaining significant insights. The systems enable labs to sequence on demand and analyse samples on the same day.

The MiSeq i100 Series improves the MiSeq System’s legacy with the NovaSeq™X Series technology’s newer version. It uses room-temperature storage and shipping, which provides greater flexibility for project planning and execution. The MiSeq i100 Plus can run as much as 100 million single-end reads per run while the MiSeq i100 configurations can run 25 million. The MiSeq i100 sequencing system is expected to be rolled out in 2025. This sequencing equipment will have the following benefits:

  • Room-temperature reagent shipping and storage reduce the need for a cold chain and enable on-demand sequencing
  • Reduction in packaging waste by 85%, which reduces carbon footprint
  • Reduced run times by up to four hours, with same-day results
  • Cost-effective consumables enable affordable sequencing
  • Up to 18 proven workflows across 10 applications
  • Provides efficient operations for various sequencing experience levels

MiSeq i100 also offers push-button workflows for microbiology and infectious disease/oncology, providing metrics directly on the instrument or via cloud- based DRAGEN™ genomic data analysis, reducing bioinformatics expertise requirements.

Related post

What Does Medtronic’s CE Mark Approval for the Endoflip System Mean for Patients?

What Does Medtronic’s CE Mark Approval for the Endoflip…

Highlights Medtronic has received CE Mark approval for its next-generation Endoflip 300 system for oesophageal diagnostics The Endoflip 300 System helps…
How Will the UK’s New Draft Medical Devices Regulations Impact the Healthcare Industry?

How Will the UK’s New Draft Medical Devices Regulations…

Highlights MHRA has launched a consultation on new regulations for medical devices and in vitro diagnostics Baroness Gillian Merron emphasises these…
How Magnetic Actuators are Revolutionising Modern Medical Technology?

How Magnetic Actuators are Revolutionising Modern Medical Technology?

Highlights Magnetic coupling eliminates connections, boosting efficiency in implants and minimally invasive tools Regulatory guidelines ensure safety, emphasising electromagnetic compatibility and…