Our Genefficiency high throughput CNV service combines the power of oligonucleotide array comparative genomic hybridisation (aCGH) with unparalleled expertise and sample processing capabilities to help you reliably identify biologically significant CNVs.
Genefficiency offers:
- Superior sensitivity of detection of de novo CNVs*
- More comprehensive genome coverage*
- More accurate quantification of copy number changes*
- Customised array content for your project (whole genome or focussed regions)
- High quality, high throughput CNV analysis service with >30 QC checks on each sample*
*in comparison to alternative SNP based approaches. See data
Register your details and we will contact you to discuss your CNV requirements
OGT Genefficiency aCGH service for CNV analysisThe PLATFORMCustomise your content from our library of >24 million high resolution CNV probes spanning the entire genome. Read more The PERFORMANCEaCGH locates more chromosomal breakpoints at higher resolution, and quantifies copy number changes more accurately than any other method. Read more The PROCESS POWERWith the capacity to run >1,000 samples per week (with >30 QC checks on each sample) and deliver high quality data quickly, OGT are the service provider for CNV studies. Read more The PEOPLEOur dedicated, experienced scientists are available for consultation and support throughout your project. Ask us a question |
Useful links...
- New study confirms OGT's Agilent aCGH platform as better than SNP-based CNV quantification approaches.
- Find out more on aCGH for CNV with our Q & A sheet
- Discover more about CNV at our resource portal
- View our satisfied Genefficiency customers
Win a Sony camera†
Discover how OGT can bring your CNV analysis into focus and get your chance to win 1 of 3 Sony Cyber-shot™ digital cameras