A state-of-the-art copy number variation (CNV) analysis service

OGT's Genefficiency™ service allows high-quality detection of CNVs at high throughput

We supply a cost-effective, state-of-the-art CNV analysis service for your association study, with rapid turnaround time, rigorous quality control and a sample throughput to suit your project — from 1 to 1,000s of samples per week.

Use our personalised analysis service for your association studies to discover inherited and de novo copy number variations in the human genome and their link to disease.

The service is ideal for your molecular genetic studies of complex diseases e.g. in the areas of neuroscience and oncology.

Why carry out CNV analysis?

Differences in genomic copy numbers have been
known and studied for many years with increasing evidence that small chromosomal imbalances leading
to genomic copy number variation (CNV) are common
phenomena, affecting as much as 12% of the human
genome. In addition to reports of the presence of
CNVs in healthy individuals, many studies have
associated CNVs with disease phenotypes, particularly
for neurobiological conditions such as autism
and schizophrenia. Read more...