Clinical Whole Exome Sequencing

Clinicians need fast and cost-effective reports that provide actionable clinical insights.

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Genetic testing via clinical whole exome sequencing (WES) is leveraged for healthcare more now than ever.

Your sequencing provider needs to provide:

  • Clinically insightful findings and actionable recommendations
  • Quick turnaround of data and reports
  • Cost-effective data and reporting options for physicians, medical geneticists and patients

Clinicians need answers to genetic questions, and they are looking for answers quickly and reliably. Having a trusted partner who can provide these answers quickly in the most cost-effective manner is key for clinicians around the world.

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 You Need:

  • Primary Findings
  • Secondary Findings
  • Incidental Findings (optional)
  • Follow-up recommendations

Email us at [email protected] for more information on our clinical exome sequencing, and please be sure to specify your interest in diagnostic use.

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