Sequencing services for Whole Genome and Whole Exome research use
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