Applications
including CNV, aCGH, miRNA, gene expression and methylation studies
Application: Copy number variation (CNV)
Click on the images below to see a larger view of each screenshot
Above: screenshot of CytoSure™ Interpret Software* indicating an approximate 130kb deletion in a known region on chromosome 8. The CNV has been identified with only 5 probes.
Above: screenshot of CytoSure™ Interpret Software indicating an approximate 1Mb deletion in a known CNV region on chromosome 15.
* CytoSure Interpret Software — OGT's comprehensive and intuitive analysis software, allowing easy interpretation of aCGH data.
Case Study: Wellcome Trust Case Control Consortium
| 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.... |
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