Bionano Saphyr optical genome mapping system

Optical genome mapping resolves large-scale structural variations missed by NGS systems

The Saphyr system is a genome imaging tool for high-speed, high-throughput structural variant detection and analysis with exceptional sensitivity and specificity.

Saphyr optical genome mapping offers automated features that minimize hands-on time.

  • From sample to whole genome analysis in just 3 to 4 days with the new G2 sample preparation kits
  • Automatic optimization of run conditions based on sample characteristics maximizes throughput
  • Saphyr Chip Clip protects sample integrity and eliminates the need for instrument wash cycles between runs

Wide range of applications for human, plant and animal genome mapping

  • Undiagnosed genetic disorders
  • Hematologic malignancies
  • Gene discovery and therapy
  • Cell line stability
  • Solid tumor research
  • Genetic engineering studies
  • Evolutionary biology
  • Reference genome assembly

Built using proprietary Nanochannel technology, Bionano Chips for the Saphyr system linearize DNA, enabling high-speed, high-throughput optical genome mapping and structural variation detection for a variety of applications including human and clinical research.

Bionano G2 Prep Kits provide the critical reagents and protocols needed to extract and label high molecular weight (HMW) DNA for use on the Saphyr system. Bionano kits are optimized for performing Bionano optical genome mapping applications on a variety of sample types.

Bionano Data Solutions includes a complete suite of hardware and software for end-to-end experiment management, analysis and bioinformatics processing, along with convenient web-based management and monitoring tools.

Bionano Access

  • web-based hub for Saphyr operations, provides all the software you need for experiment management and Bionano optical genome mapping in one place

Bionano Compute On Demand

  • pay-per-use solution accessible through Bionano Access web server for your Bionano Solve operations

VIA™ software

  • combines secondary and tertiary analysis, receiving and interpreting data from optical genome mapping (OGM), next-generation sequencing (NGS) and microarrays to contextualize all classes of genomic variation and drive meaningful insights.

Product is available in the following countries:

  • Finland
  • Estonia
  • Latvia
  • Lithuania

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Keywords

cancer inherited diseases

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