Sequencing Capabilities
Complete Genomics’ disruptive human DNA sequencing technology is being deployed on a large scale in
its unique genome center. Complete Genomics’ unprecedented throughput provides ultra-deep sequencing
coverage with many overlapping reads and confident variant detection, enabling sequencing of large
numbers of individuals for medical or clinical studies.
Sequencing Service Enhancements
Complete (six-billion base) human genome sequencing has a number of uses:
- Genome subsetting, such as candidate region or exon/gene/transcriptome
sequencing from a large number of samples
- Structural variation and copy number variation (CNV) analysis
- Genomic rearrangements and allelic imbalances
- Separate sequencing of each parental chromosome for accurate prediction
of the functional impact of genetic changes
Potential Uses of Whole Genome Sequencing
Complete Genomics’ high-throughput, affordable sequencing service opens the door to exciting human
genome resequencing applications:
- Population variation discovery in medical studies and clinical drug trials
- Sequencing detects variants not observed by conventional microarrays, e.g.,
closely spaced SNPs or long variations. Disease association studies and other uses of variant
detection will benefit from a more accurate and thorough analysis of genomic data.
- Cancer genome analysis (see Future Applications)
- Genotyping
- Functional genomics
Customer Support
Complete Genomics’ genome center is designed and staffed to help researchers maximize the
full potential of their efforts with:
- Consultation on data analysis and bioinformatics applications
- Staff with broad and deep technology expertise and extensive sequencing
applications experience
- Consultation before, during and after a sequencing project
- Consultation on experimental design, ongoing research and collaborations to
expand the applications portfolio and number of completed sequences
- Assistance with preparation of sequence data for publication and sequence
submission to public databases
For more information on Complete Genomics’ services, please
contact info@completegenomics.com.
Top of page