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Explore a wide range of free and certified Genetics online courses. Find the best Genetics training programs and enhance your skills today!
Explore exome sequencing for congenital anomalies and neurodevelopmental disorders, comparing testing methods, discussing clinical implementation, and examining diagnostic yields for various patient populations.
Genetic counselors discuss transitioning between telehealth and in-person care during COVID-19, sharing experiences from various specialties and locations to address medical and social impacts on patients and providers.
Explore key compliance laws for molecular genetic testing labs, covering Anti-Kickback, Stark Law, and HIPAA. Learn practical applications and data privacy considerations in the laboratory setting.
Explore structural biology's role in variant assessment, focusing on biophysical methods to evaluate protein function disruption and reclassify variants of unknown significance.
Comprehensive overview of genetic risk assessment in prostate cancer, covering polygenic risk scores, rare pathogenic mutations, and their clinical implications for personalized screening and treatment.
Learn to transition your genetics clinic to telehealth, covering virtual care options, HIPAA guidelines, billing codes, and best practices for patient care in a remote setting.
Explore advancements in RNA genetic testing for clinical diagnostics, covering molecular biology, targeted approaches, and case studies demonstrating increased diagnostic yield in tumor suppressor genes.
Explore a systematic framework for interpreting copy number variants in genetic testing. Learn about proposed updates to guidelines, evidence-based evaluation, and improving interlaboratory consistency.
Explore hereditary cancer genetics, testing technologies, and implications for breast and gynecologic cancers. Learn about key genes, risk factors, and the impact on medical management.
Explore cardiovascular genetics, genetic testing's clinical utility, and key inherited conditions in this informative webinar led by a specialized genetic counselor.
Explore genetic high cholesterol: symptoms, diagnosis, genetics, testing, and treatment. Learn about familial hypercholesterolemia and its impact on cardiovascular health.
Learn exome sequencing technology, lab processes, and applications. Explore data formats, variant filtering, gene-disease prioritization, and report structure. Gain insights into unique aspects and advantages of exome sequencing in genetic diagnostics.
Comprehensive overview of Spinal Muscular Atrophy, covering genetics, diagnosis, and recent therapeutic advancements. Explores disease etiology, new FDA-approved treatments, and their impact on patient outcomes.
Explore clinical and genetic risk factors for contralateral breast cancer, focusing on family history, genetic mutations, and risk prediction models. Learn to apply these insights in clinical settings.
Demystifying bioinformatics concepts in genetic testing reports, focusing on key terminology and underlying details for NGS panel and exome-sequencing tests to enhance clinicians' understanding and interpretation.
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