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Diagnostic Solutions.
National cancer care guidelines recommend hereditary cancer screening for early identification when prevention and treatment are most effective.
But guidelines are complicated, dynamic and can be challenging to integrate into clinical practice.
We can help you easily screen patients to determine if they are at increased risk of developing cancer due to hereditary genetic changes.
Tumor profiling genetic tests play a pivotal role in the management of cancer patients by providing crucial insights into the genetic makeup of tumors.
These tests help identify specific genetic mutations driving cancer growth, allowing oncologists to tailor treatment strategies accordingly.
By understanding the unique molecular characteristics of each tumor, healthcare professionals can prescribe personalized therapies that are more effective and less toxic, ultimately improving patient outcomes.
Offering broad-panel DNA and RNA-based next-generation sequencing (NGS) for your oncology testing requirements.
A complete spectrum of testing options: The most comprehensive combination of tests spanning from single-gene, disease-specific and broad reach tumor profiles in tissue and plasma specimens, in addition to bone marrow and peripheral blood samples.
Full-range molecular diagnostic technologies: NGS is a molecular methodology that is part of a broader family of molecular tests. In addition to NGS, Virotek provides a wide array of quantitative PCR, Sanger sequencing, and send-out SNP microarray services.
Even though medications might be labeled as one size fits all, they aren’t when it comes to effectiveness, dosage and side effects. People experience medications differently, which often leads to a trial-and-error period to find the right medication.
Pharmacogenomics testing can help you guide your patient to the right medication and dosage more quickly. We can help your patient understand pharmacogenomic testing and whether the results indicate their unique genetic makeup may impact medication efficacy.