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Explore genomics-driven approaches to developing improved cancer vaccines, focusing on cutting-edge research and potential clinical applications in personalized immunotherapy.
Explore whole genome methylation profiling for CNS tumor classification. Learn about workflow, data analysis, and clinical applications in this comprehensive genomics presentation.
Explore leveraging SNP arrays in cancer genomics beyond CNVs, focusing on mosaic gains/losses, HRD scores, and noninformative SNPs for improved diagnosis and treatment.
Explore high-resolution DNA analysis for clonal hematopoiesis. Learn about mutational hierarchy, precision medicine, and clinical applications in cancer and bone marrow failure.
Explore comprehensive genomic profiling solutions for cancer diagnosis, focusing on internalizing processes, overcoming challenges, and securing reimbursement pathways.
Explore advances in diagnosing and treating Neurofibromatosis 1, covering mutation spectrum, pathogenesis, clinical trials, and future opportunities in this comprehensive keynote presentation.
Explore SNP array analysis techniques for borderline melanocytic tumors, enhancing diagnostic accuracy and treatment decisions in cancer genomics.
Explore optical genome mapping and NGS integration for leukemia and lymphoma clinical research. Learn from expert panelists about advanced genomic techniques in cancer diagnostics.
Explore innovative approaches to developing next-generation biomarkers for cancer diagnosis and treatment, enhancing precision medicine and patient outcomes.
Explore integrative cytogenetic and molecular studies revealing 'Chromosomal Mimicry' in hematologic malignancies, enhancing accurate diagnosis and targeted therapy for cancer patients.
Learn to implement ClinGen/CGC/VICC Oncogenicity Guidelines for pediatric variant classification, enhancing accuracy in cancer genomic testing and improving patient diagnosis and treatment outcomes.
Explore rapid molecular testing strategies to address pediatric cancer disparities in Sub-Saharan Africa, focusing on improved diagnosis and treatment outcomes.
Explore cytogenetically cryptic oncogenic fusions in pediatric AML, examining their frequency and etiology to enhance diagnostic accuracy and treatment approaches.
Explore the prognostic impact of MYC copy number gain in large B-cell lymphoma through FISH analysis, enhancing diagnostic accuracy and treatment decisions.
Explore genomic and epigenomic analysis of cell-free DNA to predict survival in metastatic castration-resistant prostate cancer patients undergoing AR-directed therapy.
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