The Bionano Saphyr® system

Detects structural variations in an unbiased manner at much higher sensitivities than sequencingbased
technologies, down to 500 bp resolution and routinely at 5% variant allele fraction.

  • Detect genome-wide SVs at >10,000x higher resolution over karyotyping
  • Detect genome-wide CNVs and fusions, including fusion partners.
  • Identify genes of interest, their locations, and how SVs impact them, for effective therapy development
  • Detect somatic rearrangements in heterogeneous tumors at 5% variant allele fraction
  • A workflow alternative to multiple traditional cytogenetic methods

Biomark X The new benchmark in genomics

Biomark™ X and a portfolio of integrated fluidic circuits (IFCs) and reagent kits facilitate a broad range of applications and throughput needs using real-time PCR

  • Throughput from 120 to more than 1000 samples/day
  • Validated Kits for nucleic acid extraction
  • Flexible sample volume range from 10 µl to 10 ml
  • User-friendly interface

Maelstrom Switch 8, an open system automated nucleic acid extractor.

TANBead’s spin-mixing patented technology prevents the risk of sample cross-contamination.
Open for various reagent kits offer more flexibility to adapt
representative brands magnetic bead-based reagent kits and applications.

  • Whirl Stirring Mixing Technologyividual cells to separate reaction chambers.
  • Switchable magnetic rods (4/ 8/ 16 channels)ages the IFC to confirm cell count, viability or phenotype.
  • Flexible sample volume range from 0.05ml to 20ml
  • Protein purification/ Cell isolationnt for sequencing or qPCR detection.

Innovative products for high throughput single cell research

Droplet Based scRNA-Seq methodology. Using droplet microfluidics, achieves unprecedented access to the transcriptomes of thousands of single cells.  

  • High throughput – 5,000 – 10,000 single cell transcriptomes per run
  • High capture rate
  • Fully automated sample encapsulation
  • Processing capability of up to 8 samples in parallel.
  • Easy-to-use

Automated NGS Library Prep Workstations

 True walkaway library prep with easy-to-use,
proven methods for nearly all sequencing platforms.

  • Sample Capacity: from 8 to more than 96 samples per day
  • open-design format
  • field reconfigurable
  • intuitive interface

NEXTflex® library preparation kits

NEXTflex® library preparation kits are designed to reduce bias and increase the sensitivity, flexibility, and speed of library prep for both Illumina® and Ion Torrent™ sequencing platforms.

  • DNA Sequencing Library Prep
  • RNA Sequencing Library Prep
  • Small RNA Sequencing Library Prep
  • Metagenomics
  • Epigenetics
  • Amplicon Panels

LabChip GX Touch Nucleic Acid Analyzer

DNA and RNA quantitation and sizing can be done in seconds using automated capillary electrophoresis separation.

  • NGS library preparation (smear and fragment analysis) and quality control
  • RNA and DNA fragment analysis (including cell-free (cfDNA), FFPE, liquid biopsy, and PCR-free samples)
  • Quantitation and qualification for CRISPR fragment analysis
  • Agarose gel workflows