Precision Diagnostic
Services
for Modern Clinical Care
Molecular infectious disease panels, hereditary NGS genomics, and pharmacogenomics — organized so you can match the right test to every clinical scenario.
Find the Right Testing Path.
Select the scenario that best matches your patient — we will guide you to the appropriate service category.
Infection Symptoms
UTI, STI, wound, respiratory, or GI pathogens
ExploreHereditary Risk
Family history of inherited disease
ExploreMedication Response
Adverse events or ineffective dosing
ExploreFamily History
Cascade screening and proactive care
ExploreTreatment Failure
Recurrent infection or resistance concerns
ExploreThree Core Service Pillars.
Every Vdiagnostics test fits one of three clinically distinct pathways — each engineered for speed, accuracy, and actionable reporting.
Molecular Testing
High-sensitivity q-PCR panels for infectious disease — pathogen ID and resistance profiling in 48 hours.
- Turnaround
- 48 Hours
- Specimen
- Urine, swab, wound, respiratory
- Best for
- Acute infections, recurrent UTI, wound care, RPP
NGS Hereditary Genomics
Clinically curated multi-gene panels across organ systems — identify variants and guide family risk management.
- Turnaround
- 7–10 Business Days
- Specimen
- Buccal swab / saliva
- Best for
- Family history, syndromic presentation, surveillance planning
Pharmacogenomics (PGx)
30-gene comprehensive profiling to predict drug response and reduce adverse drug events.
- Turnaround
- Standard Lab TAT
- Specimen
- Buccal swab / saliva
- Best for
- Polypharmacy, psychiatric meds, cardio-oncology Rx
Rapid Pathogen Detection.
Modular q-PCR panels with resistance profiling — engineered for 48-hour turnaround and targeted therapy decisions.
UTI/STI Panel
Comprehensive molecular detection of urinary tract and sexually transmitted infections with resistance screening.
Specimen: Urine
Advanced Wound Care
Rapid pathogen identification and resistance profiling for optimal wound management.
Specimen: Wound swab
Nail Fungal Detection
Accurate diagnosis of dermatophyte, yeast, and non-dermatophyte mold infections.
Specimen: Nail clipping
Next-Generation Sequencing Panels.
Identify inherited risk, personalize care, and enable proactive family screening across 11 organ-system panels.
Hereditary Cancer Genomics
Multi-gene panels for inherited cancer syndromes — earlier surveillance and precision oncology planning.
Hereditary Cardiovascular
Cardiomyopathies, channelopathies, and familial hypercholesterolemia.
Hereditary Pulmonological
Cystic fibrosis, alpha-1 antitrypsin deficiency, and inherited lung disorders.
Hereditary Renal
Inherited kidney disease and polycystic kidney syndromes.
Hereditary Neurological
Hereditary neuropathies, ataxias, and neurodegenerative risk.
Monogenic Diabetes (MODY)
Maturity-onset diabetes of the young and monogenic hyperglycemia.
Hereditary Metabolic
Inborn errors of metabolism and inherited metabolic pathways.
Hereditary Eye Disorders
Inherited retinal dystrophies and ocular genetic syndromes.
Hereditary ENT Disorders
Sensorineural hearing loss and syndromic ENT presentations.
Genomic Intelligence for
Precision Treatment.
Not every medication works the same for every patient. Our PGx profiling analyzes genetic variations to predict efficacy and reduce adverse drug events.
- Personalized medicine based on patient DNA
- Identify optimal drug and dosage immediately
- Minimize adverse drug event risk
- 30-gene comprehensive panel available
Cardiovascular Panel
Medication insights for cardiovascular treatment planning.
9 genesPsychiatric Panel
Medication response guidance for psychiatric therapies.
14 genesOncology Pharmacogenomics
Support treatment planning for oncology medications.
4 genesPain Management & Deaddiction
Medication response support for pain and addiction therapy.
3 genesHow Ordering Works.
One streamlined process for molecular, NGS, and PGx — from requisition to secure digital results.
Request Test
Digital or paper requisition integrated with your EMR workflow.
Provider Approves
One-click clinical authorization via our secure provider portal.
Lab Processes Sample
High-speed molecular extraction, NGS sequencing, or PGx analysis.
Results Delivered
Secure digital reporting with actionable clinical insights.
Uncompromising Quality Standards.
Rigorous clinical certification, secure reporting, and dedicated pre-authorization support for every service line.
HIPAA Compliant
Encrypted Architecture
CLIA Certified
Federal Quality Standards
SOC 2 Ready
Data Security Protocol
Molecular Lab
High-Complexity Testing
Dallas, TX
State-of-the-Art Hub
What Providers Receive
- Clear result summary with clinical interpretation
- Pathogen or gene-level findings with significance
- Resistance markers or metabolizer status where applicable
- Suggested next-step care and family screening guidance
Insurance and pre-authorization support available for all service categories.
Frequently Asked Questions.
Start with the clinical need: acute infection symptoms point to molecular panels; family history or syndromic presentation suggests NGS hereditary genomics; medication failures or polypharmacy suggest PGx. Use the service finder at the top of this page to jump to the right category.
Molecular infectious disease panels typically return within 48 hours. NGS hereditary panels are delivered in 7–10 business days. PGx turnaround follows standard lab processing with secure digital delivery to the ordering provider.
Most commercial plans and Medicare cover molecular and hereditary testing when clinical necessity criteria are documented. Vediagnostics provides dedicated pre-authorization support to help navigate coverage requirements.
Results are delivered securely to the ordering provider through our digital portal. Patients may access authorized results via the patient portal when enabled by your practice.
Molecular panels typically use urine, wound swabs, respiratory swabs, or stool. NGS and PGx panels commonly use buccal swab or saliva — no blood draw required for most hereditary and pharmacogenomic tests.
Ready to Match the Right
Test to Your Patient?
Request testing, explore panel details, or connect with our team for clinical and coverage support.