Cancer Genomics
Testing
Understanding Your Tumor at the Molecular Level
Coverage
96% at 20x
Sample Type
Buccal / Saliva
Cancer is complex—but treatment should be smarter.
Advanced genomic sequencing helps identify the specific genetic mutations driving tumor growth, enabling more personalized treatment strategies, targeted therapies, and improved clinical outcomes.
Why Cancer Genomics Testing Matters
Precision Treatment
Identify targeted therapies based on tumor mutations.
Molecular Understanding
Understand the genetic drivers behind tumor behavior.
Family Risk Detection
Identify hereditary cancer risks for family members.
Better Outcomes
Personalized treatment may reduce side effects and improve results.
How Cancer Genomics Testing Works
Sample Collection
Buccal swab or saliva sample collected.
DNA Sequencing
Advanced NGS sequencing analyzes genetic mutations.
Mutation Analysis
Data compared against known cancer-related databases.
Clinical Insights
Providers receive precision-based treatment planning reports.
Personalized Care
Targeted therapy decisions based on molecular findings.
Cancer Types We Screen For
We leverage next-generation sequencing to evaluate high-risk mutations associated with multiple complex hereditary cancer pathways.
Breast Cancer
Target PanelOvarian Cancer
Target PanelProstate Cancer
Target PanelLung Cancer
Target PanelPancreatic Cancer
Target PanelColorectal Cancer
Target PanelStomach Cancer
Target PanelBladder Cancer
Target PanelMelanoma
Target PanelLynch Syndrome
Target PanelHereditary Cancer Gene Panel
38 clinically relevant genes analyzed through advanced genomic sequencing to evaluate cancer predisposition.
Core Target Genes
Our panel checks these essential genes known to be primary drivers of hereditary breast, ovarian, colorectal, and prostate cancer pathways.
View Full 38-Gene Panel
Deeply index your search or review the full set of genes processed in this panel according to ACMG compliance.
Test Specifications
Sample Type
Buccal Swab / Saliva
Reporting
Pathogenic & Likely Pathogenic Variants
Turnaround Time
7–10 Business Days
Coverage
96% at 20x
Customizable Gene List
Provide diagnostic targeted panels aligned directly to your patient's family history or diagnostic path. Our team supports custom EMR-portal integrations, allowing specific sub-requisition panels.
Why Providers Choose
Cancer Genomics
Improved Diagnosis Accuracy
More precise clinical decisions.
Personalized Treatment
Target therapies aligned to mutation profile.
Family Risk Assessment
Identify inherited cancer predispositions.
Faster Decision Making
Rapid insights for time-sensitive care.
If Genetic Testing Finds
Elevated Risk
We focus on reducing anxiety. A positive variant finding is not a diagnosis of cancer; it is a powerful roadmap to build a highly optimized preventative pathway.
Confirm Findings
Validate identified variants through rigorous clinical review.
Physician Consultation
Collaborative review of clinical pathways with your provider.
Personalized Care Planning
Tailor medical therapies and precision surveillance strategies.
Family Risk Evaluation
Initiate directed cascade screening for first-degree relatives.
Preventive Care Strategy
Establish early cancer surveillance and risk-reducing paths.
Understanding Genetic Testing
What is Genetic Testing?
Genetic testing analyzes your DNA to identify specific hereditary variations (mutations) that significantly increase your susceptibility to developing particular cancer types. It determines inheritance pathways.
Why Is It Important?
Understanding genetic mutations early allows you and your healthcare provider to design tailored clinical screening protocols, introduce lifestyle risk reductions, or consider preventive medical paths.
Testing Outcomes
Results can be Positive (variant found), Negative (no high-risk variant identified in tested genes), or Uncertain (Variant of Uncertain Significance - meaning a change is detected but its clinical impact is undefined).
Personalized Medicine
Precision medicine utilizes your genomic data to customize clinical surveillance. It targets specific risk markers directly and removes ineffective one-size-fits-all medical approaches.
Insurance Information
Vediagnostics simplifies laboratory billing. We work directly with insurance providers to secure maximum coverage options for patients.
- Verify commercial policy coverage
- Identify physician clinical recommendation
- Process secure laboratory prior authorizations
Frequently Asked Questions
Precision Cancer
Insights Start Here
Early molecular understanding can lead to better treatment decisions, improved outcomes, and personalized care.