Genefficiency Plus — it's in our DNA

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Genefficiency™ Plus offers the complete service for high throughput microarrays through a unique combination of:

  • Industry-leading platforms
  • Highly skilled people
  • Unparalleled process power

Why Choose Genefficiency™ Plus?

Genefficiency vs Genefficiency Plus
Expert Team — our scientific team has benefited from many years in the genomics industry
Yes
Yes
Multi-disciplinary focus — each project receives input from a broad range of disciplines
Yes
Yes
Fully automated workflow — increases sample throughput
No
Yes
Proprietary software — to facilitates fast, effective, and intuitive data access
No
Yes
Standard quality control — all Genefficiency services incorporate a rigorous QC infrastructure
Yes
Yes
Quality control Plus — comprised of 20 sample QC steps, >30 in-process QC checks, and 15 validation steps* No Yes
LIMS software — tracks every sample through the entire experimental process Yes Yes
High sample throughput — in excess of 1,000 samples per week No

Yes

*for aCGH for CNV analysis

OGT is committed to providing high-quality data for a variety of high-throughput microarray applications. Many scientists have benefited from OGT's bespoke microarray service, from array design and synthesis through to bioinformatics support and data analysis.View our satisfied Genefficiency customers.

Our service integrates seamlessly into your research, for rapid, reliable results. We also offer full project support – from array design through to data processing.

Learn about our Genefficiency™ plus process in detail

Contact us for more information and win a Sony Cyber-shot™ digital camera

Download brochure - latest version!

Oxford Gene Technology: Proven pedigree with the Wellcome Trust Case Control Consortium.

- a collaboration of leading geneticists seeking to identify genetic variants influencing disease susceptibility in a broad range of complex diseases

- WTCCC standardised this major study on Agilent microarrays — OGT supplied microarray services read more...

» Major CNV study published in Nature uses OGT's CNV service:

Origins and functional impact of copy number variation in the human genome

Nature advance online publication
Oct 7, doi:10.1038/nature08516.