Sequencing services for Whole Genome and Whole Exome research use

May 9, 2024

Note: Blueprint Genetics does not offer this service in the US at this time 

Our certified laboratory delivers sequencing services from whole genomic sequencing (WGS) and whole exome sequencing (WES) for research use.

Our goal is to provide you with sequencing services necessary to transform and expedite your research.

WGS sequencing service

Our best-in-class technology delivers sequencing services for WGS research that provide a comprehensive view of genetic makeup, empowering your team to quickly and reliably identify relevant information that supports your study goals.

  • Main sequencing coverage of WGS is ≥30x throughout the entire genome (minimum acceptable average read depth of 25x)
  • >98% of the targeted bases are covered at >15x
  • ≥95% of bases with quality score of ≥Q30

WES sequencing service

Our sequencing service for WES research meets the highest standards in quality and performance, helping your team to analyze the exome region of the genome.

  • 99.6% of bases are covered at 20x
  • Average sequencing depth 154x at 100M sequencing reads

To learn more about our Sequencing Services, click here.

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