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Comprehensive overview of Illumina sequencing workflow, covering library preparation, cluster generation, and sequencing by synthesis. Explores different chemistry versions and instrument developments for next-generation sequencing.
Explore genetic diagnoses in epilepsy care, their impact on treatment options, and the latest advancements in precision medicine for various epilepsy syndromes.
Explore cardiovascular genetic testing, result interpretation, and clinical applications through case studies, focusing on family history analysis and cascade testing implications.
Explores racial and ethnic differences in cancer genetic testing results for breast cancer patients, highlighting opportunities to improve testing utility in populations facing health inequalities.
Explore advances in genetic testing for prostate cancer, including risk prediction, precision therapies, and genetic counseling. Learn about implementation strategies and guidelines for germline testing in prostate cancer care.
Explore innovative techniques in hereditary cancer detection, including RNA genetic testing and AI-powered risk assessment, to improve diagnostic yield and patient identification for genetic counseling.
Comprehensive overview of hATTR amyloidosis, covering diagnosis, management, and genetic aspects. Experts discuss clinical presentations, genotype-phenotype correlations, and genetic counseling challenges for patients and families.
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.
Exploring digital tools for efficient dissemination of genetic counseling information in precision medicine, addressing challenges in access and timely updates for clinicians and patients.
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.
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