Precision Testing. Proactive Care.
At Preventive Genomics, we provide accurate, cutting-edge testing for a wide range of conditions. Using advanced technologies, we deliver reliable results to support your healthcare decisions.
Our molecular diagnostic services are centered around two key areas: Genetic Risk Assessment and Infectious Disease Testing, designed to help clinicians make timely, confident decisions.
Genetic Risk Assessment
We offer comprehensive genetic risk assessment services designed to identify inherited health tendencies and potential future risks. This process helps individuals gain a deeper understanding of how genetics may influence overall health, allowing for informed preventive actions and ongoing monitoring.
Next Generation Sequencing (NGS) has transformed genetic testing by enabling fast, accurate, and comprehensive analysis of DNA. It allows laboratories to analyzes multiple genes simultaneously to detect single nucleotide variants (SNVs), insertions and deletions (indels), copy number variations (CNVs), and other inherited mutations. By identifying pathogenic variants early, NGS provides actionable insights for hereditary cardiac, renal, eye, thyroid, metabolic, neurodegenerative, and cancer risks.
Key Benefits:
Clinical Focus Areas:
Next Generation Sequencing (NGS) has transformed genetic testing by enabling fast, accurate, and comprehensive analysis of DNA. It allows laboratories to analyzes multiple genes simultaneously to detect single nucleotide variants (SNVs), insertions and deletions (indels), copy number variations (CNVs), and other inherited mutations. By identifying pathogenic variants early, NGS provides actionable insights for hereditary cardiac, renal, eye, thyroid, metabolic, neurodegenerative, and cancer risks.
Key Benefits:
- Early identification of genetic predispositions
- Support for preventive and personalized care strategies
- Improved patient engagement through actionable insights
- Enhanced long-term health planning
Clinical Focus Areas:
- Genetic risk assessment and preventive health
- Rare and inherited disorders
- Pharmacogenomics
- Oncology and precision medicine
- Carrier screening
Personalized Health Insights
Genetic information is translated into clear, meaningful insights tailored to each individual. These insights guide lifestyle choices, preventive care planning, and informed discussions with healthcare professionals.
NGS provides detailed profiling of inherited genetic risk factors, including hereditary cardiac, renal, eye, and thyroid disorders. Pharmacogenetic testing adds an extra layer of personalization by revealing how an individual’s genetic makeup may affect medication response, helping optimize treatment plans and reduce side effects.
NGS provides detailed profiling of inherited genetic risk factors, including hereditary cardiac, renal, eye, and thyroid disorders. Pharmacogenetic testing adds an extra layer of personalization by revealing how an individual’s genetic makeup may affect medication response, helping optimize treatment plans and reduce side effects.
Preventive Health Guidance
Our services provide actionable guidance based on genetic and infectious disease findings. This supports informed decision making related to nutrition, physical activity, monitoring strategies, and preventive care planning, helping individuals reduce long term health risks.
Long Term Health Planning
Preventive genomics supports a future-focused approach to health. Understanding genetic risk factors early allows individuals and families to plan ahead and take steps to reduce potential health challenges over time.
Scientific Accuracy and Data Privacy
All preventive genomics services are based on validated scientific methodologies and high-quality laboratory standards. Preventive Genomics is CAP accredited and CLIA certified clinical diagnostic lab.
NGS sequencing provides high coverage depth for accurate variant detection, while PCR testing uses pathogen-specific primers and real-time amplification for sensitive and precise identification. Together, these technologies deliver clinically actionable results you can trust.
We follow strict data privacy and security protocols to ensure genetic and infectious disease information is handled responsibly and confidentially.
NGS sequencing provides high coverage depth for accurate variant detection, while PCR testing uses pathogen-specific primers and real-time amplification for sensitive and precise identification. Together, these technologies deliver clinically actionable results you can trust.
We follow strict data privacy and security protocols to ensure genetic and infectious disease information is handled responsibly and confidentially.
Infectious Disease Testing
Faster Answers When Timing Matters Most
Preventive Genomics offers highly sensitive molecular testing solutions for the rapid detection of infectious pathogens. Using advanced RT-PCR based methodologies, our assays identify infections early and accurately, even at low pathogen levels—supporting prompt intervention and improved patient management.
What Sets Our Testing Apart:
Clinical Focus Areas:
Our molecular infectious disease testing helps providers deliver targeted therapies, reduce unnecessary treatments, and enhance overall quality of care.
Preventive Genomics offers highly sensitive molecular testing solutions for the rapid detection of infectious pathogens. Using advanced RT-PCR based methodologies, our assays identify infections early and accurately, even at low pathogen levels—supporting prompt intervention and improved patient management.
What Sets Our Testing Apart:
- High sensitivity and specificity for confident clinical decisions
- Rapid turnaround times to support timely treatment
- Early detection for improved patient outcomes
- Reliable performance across a wide range of pathogens
Clinical Focus Areas:
- Respiratory infections
- Urinary Tract infections
- Sexually transmitted infections (STIs)
- Community-acquired infections
- Detection of antibiotic-resistant genes for appropriate treatment.
Our molecular infectious disease testing helps providers deliver targeted therapies, reduce unnecessary treatments, and enhance overall quality of care.
Pharmacogenetic Testing
Pharmacogenetic testing focuses on how an individual’s genetic makeup affects medication response. It helps identify genetic variations that influence drug effectiveness, dosage requirements, and the risk of adverse reactions.
Using pharmacogenetic insights, healthcare providers can make safer prescribing decisions, improve treatment outcomes, and reduce trial and error in medication selection. This contributes to personalized medicine and better long-term health management.
Using pharmacogenetic insights, healthcare providers can make safer prescribing decisions, improve treatment outcomes, and reduce trial and error in medication selection. This contributes to personalized medicine and better long-term health management.
