Our mission is to facilitate the use of genetic testing in clinical practice. We believe that carefully prescribed genetic testing can play a vital role in the care process by
- allowing a definitive diagnosis
- assisting in the selection of therapies or preventative measures
- detecting a predisposition for disease
- identifying carriers and enabling early diagnosis in affected family members
Genes That Matter™
We select genes for testing based on clinical utility.
Innovative Technologies
Our automated high-throughput processes allow
- Rapid and reliable DNA sequence analysis
- Accurate and consistent result interpretation and reporting
- Short turn-around times
Full Sequence Analysis
- Our testing is based on PCR amplification and DNA sequencing on a robotic platform. We sequence the entire protein-coding region of a gene to reduce incidence of false negative results and to expand knowledge of genetic variation.
Curated Variant Database:
- We maintain a comprehensive and dynamic database (GeneExplorer™) of gene variants and use defined protocols to score each variant for probability of association with disease.
Detailed Result Reporting:
- We generate comprehensive result reports through our rules-based reporting system, RightReport™. The system’s updating feature allows revised interpretations as knowledge about variants and their significance for disease evolves.
Informational Materials:
- We support clinicians by providing up-to-date disease overviews and clear indications for test use.
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