Genetic Testing Via Clinical Whole Exome Sequencing (WES) Is Leveraged For Healthcare More Now Than Ever
As Your Sequencing Provider We Provide
- High quality clinical exome data from our CLIA-certified clinical laboratory based in Atlanta, GA, USA
- Quick turnaround of data
- Cost-effective data and analysis options
Clinical WES Provides The Right Balance Of Insights And Price
Whole Genome Sequencing (WGS) takes too long, is often cost-prohibitive, and the data needed is usually in the exonic regions. Whole Exome Sequencing can identify genetic variants responsible for:
- Mendelian diseases such as Huntington’s disease
- Somatic variants linked to various cancers
- Diseases such as Alzheimer’s and autism which have an underlying genetic component
- Influencing an individual’s response to a specific pharmacological regimen
Let Us Help You Select And Generate The Clinical Exome Data & Reporting Options That Are Best For Your Needs
- Robust clinical reports with variant calling and clinical recommendations
- Specialized comparisons (Child/Mother/Father i.e. Trio, tumor-normal, etc.) available
Clinical WES Reports with Actionable Insights
- Primary Findings
- Secondary Findings
- Incidental Findings (optional)
- Follow-up recommendations
Email us at sales@otogenetics.com for more information on our clinical exome sequencing, and please be sure to specify your interest in diagnostic use.