For Exome Sequencing we enrich all coding regions of the human genome using Agilent Sure Select Technology. Each exome is sequenced on one Oct, Quad, or Lane, depending on the particular project or requested coverage. In addition to the enrichment and library preparation (Fragment or Paired-End) all quality controls, ePCR, sequencing on the SOLiD platform and a thorough data analysis are done by us:
- 52 MB of the human genome
- more than 99.8% of all coding exons (CCDS annotation)
- more than 90% of all reads on target
- more than 99.94% accuracy for efficient SNV calling
- Data analysis incl. mapping, SNV calling and annotation
- Turn-around-time 1-2 months
