Our clinical laboratory offers a wide range of testing services delivering accurate and timely test results.
Our clinical laboratory offers a wide range of testing services delivering accurate and timely test results.
Our mission is to provide trusted diagnostic services with compassion and care, helping individuals make informed health decisions. Our commitment is to support the well-being of our community through advanced testing, heartfelt service, and meaningful contributions to medical progress.
We use the latest technology and equipment to ensure accurate and timely results. From automated analyzers to advanced imaging systems, we invest in the best tools to provide the highest level of care.
Chief Executive Officer - Greg Ragan
Chief Financial Officer - Tavane Ragan
Chief Operations Officer - Jarvis Stephens
At Pathway Diagnostic Laboratories, our team of highly skilled professionals is dedicated to delivering quality, accuracy, and exceptional customer service. As a trusted partner for healthcare providers and research institutions nationwide, we offer a comprehensive range of advanced molecular and genetic testing services. Guided by innovation, compliance, and precision, our experts ensure every test is performed with the highest standards of care empowering better decisions and supporting optimal health outcomes. Discover the difference where expertise meets excellence.
Our strength lies in delivering high-quality, comprehensive genetic testing that goes beyond traditional diagnostics. Using advanced technologies such as PCR testing, Next Generation Sequencing, and Wound Care analysis, we provide healthcare professionals with precise and timely results to support informed treatment decisions. Equipped with state-of-the-art laboratory systems, we prioritize accuracy, speed, and patient safety while maintaining full compliance with all regulatory standards. Our commitment to excellence allows us to be a trusted partner in advancing patient care and clinical outcomes.
Pathway Diagnostic Laboratories offers a wide range of advanced diagnostic services including nasal swab, a saliva swab, and urine, to support accurate disease detection, monitoring, and treatment planning. Our state-of-the-art laboratory ensures precise results for both routine and specialized tests, continually expanding to meet evolving healthcare needs. We uphold the highest standards of confidentiality, safeguarding all patient information with strict privacy protocols. With a convenient online distribution channel and a centrally located corporate office in the heart of Texas, we make quality testing accessible, secure, and reliable for healthcare providers nationwide.
Explore answers to frequent questions for patients who have completed molecular and genetic testing, including understanding results, next steps, and how to use findings to guide personalized health care.
A polymerase chain reaction (PCR) test detects genetic material from a pathogen or abnormal cell sample. Ways of collecting samples include a nasal swab, a saliva swab, or taking a sample of blood.
Our Sexual transmitted infections panel provides detection for specification and differentiation of STD's.
This test identifies polymicrobial infections scanning the most common organisms causing UTIs and their antibiotic components.
Wound care panel identifies polymicrobial infections scanning common organisms that cause infections of the wound.
Genetic testing is used for DNA sequencing to identify changes in a DNA sequence or chromosome structure. Genetic testing can also include measuring the results of genetic changes, such as RNA analysis as an output of gene expression, or through biochemical analysis to measure specific protein output
Genetic testing for neurological disorders detects inherited DNA changes that influence brain, nerve, and muscle health.
Our primary immunodeficiency genetic test panel suits individuals with a history of frequent infections, fevers, or rashes.
Genetic testing identifies DNA variations linked to hereditary heart and lung conditions, helping assess overall cardiovascular and pulmonary risk
A genetic test that can help identify genetic variants associated with an increased risk for thyroid cancer.
Cancer genomics is a test used to identify the specific genetic mutations that drive cancer growth.
Genetic testing for metabolic disorders identifies inherited DNA changes that affect how the body processes nutrients and energy.