Whole genome sequencing allows doctors to closely analyze a patient's genes for mutations and health indicators. Learn about this procedure.
Molecular diagnostics involves analyzing DNA or RNA for red flags that can pinpoint the potential emergence of a specific disease.
Laboratory tests that used to take days to come back can now be performed instantly and accurately, using point-of-care tests.
Diagnosing leukemia in its earliest stages can improve a patient’s prognosis. Learn how this condition is diagnosed.
Cytogenic Studies are precision medicine used to diagnose leukemia at a molecular level and determine treatment options.
Parasitic diseases are infections caused by organisms that are often microscopic. Learn about symptoms and treatment.
Whether for screenings, diagnosis, or treatment for yourself or someone you care about, Yale Cancer Center offers multidisciplinary care.
Doctors only diagnose cancer after ruling out other possible causes for symptoms and performing tests to check and double-check the diagnosis. Learn more about these tests.
Inherited cancers are cancers that can be passed down from one family member to another through genes. Learn about symptoms and treatment.
Telomeres, which cap the ends of human chromosomes, may hold the key to understanding how humans age and develop diseases.