Salus BioMed

Sequencing Platforms & Spatial Transcriptomics

 

 

Key Benefits

 

  • Advanced SBS technology: new optical system, sequencing chemistry, chips, enzymes, and fluorescent labels
  • Application and service support within the EU + local application and bioinformatics support from PentaGen
  • Over 500 installations worldwide
  • Certified in accordance with IVDR and ISO 13485
  • Easy handling and seamless implementation into routine workflows
  • Compatibility with standard library preparation kits and bioinformatics tools
  • Proven output data quality
  • The widest selection of sequencing cartridges on the market, including pre-loaded sequencing chips

 

The Salus BioMed portfolio covers the full range of sequencing needs across different throughput levels.

Platforms

 

Saluseq Nimbo

 

  • The smallest and fastest
  • Flexible (capacity and sequencing modes)
  • Accurate and user-friendly
  • Certified according to IVDR and ISO 13485

 

Learn more at: pentagen.cz/en/produkt/317-saluseq-nimbo

Salus Pro

 

  • Universal mid-throughput platform
  • Two independent sequencing units
  • Comprehensive and flexible
  • Certified according to IVDR and ISO 13485

 

Learn more at: pentagen.cz/produkt/318-salus-pro

Salus EVO

 

  • Maximum throughput in minimal time
  • Two independent sequencing units
  • High-capacity platform
  • Certified according to IVDR and ISO 13485

 

Learn more at: pentagen.cz/en/produkt/319-salus-evo

 

Salus Pro Platform – Internal Comparison of WES Data Quality

Using a set of 8 samples prepared with the xGen™ Exome Hyb Panel v2 (IDT), we compared sequencing results generated on the Salus Pro platform and a reference SBS platform under the same PE150 mode.

 

Secondary data analysis showed better results in key parameters in favor of the Salus Pro platform, particularly:

  • significantly lower mismatch rate
  • higher percentage of mapped reads
  • lower duplicate read rate
  • higher data uniformity

 

At the same time, the Salus Pro platform demonstrated:

  • comparable sequencing coverage depth
  • compatibility with standard library preparation kits and bioinformatics tools, without the need for additional data conversion.