Courses from 1000+ universities
Seven years after replacing a Yale president with a fintech CEO, Coursera picks an Amazon veteran to help fix its slowing growth and falling stock price.
600 Free Google Certifications
Computer Science
Communication Skills
Graphic Design
Gamification
Introduction to Mathematical Thinking
Mechanics of Materials I: Fundamentals of Stress & Strain and Axial Loading
Organize and share your learning with Class Central Lists.
View our Lists Showcase
Explore gene-specific cancer risks, prevalence of pathogenic variants, and sensitivity of testing criteria for BRCA1/2 and Lynch syndrome based on a large multigene panel cohort study.
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 inherited cardiomyopathies, their genetic components, and management implications. Learn about diagnostic criteria, genetic testing, and clinical approaches for various heart conditions.
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.
Comprehensive overview of breast cancer risk assessment using the Tyrer-Cuzick model, covering key risk factors, recent updates, and potential applications for screening and prevention strategies.
Explore how combining DNA and RNA genetic testing enhances detection of clinically-actionable variants and reduces inconclusive results in hereditary cancer testing, improving diagnostic yield.
Explore psychosocial challenges in genetic testing decisions, communication strategies, and patient support. Learn to create personalized information plans and navigate emotional complexities across various hereditary conditions.
Explore patient-driven cystic fibrosis research, focusing on exercise as treatment. Learn how the CF community designed and funded an innovative study, empowering patients to lead meaningful research initiatives.
Explore how RNA genetic testing enhances hereditary cancer diagnostics, increasing detection of actionable variants and reducing inconclusive results through concurrent DNA and RNA analysis.
Get personalized course recommendations, track subjects and courses with reminders, and more.