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Explore somatic mutations' role in bone marrow failure and inflammation. Gain insights from David Beck's keynote on cancer genomics and its impact on patient diagnosis and treatment.
Explore TP53 alterations in myelodysplastic neoplasms and acute myeloid leukemia, gaining insights from expert Joseph Khoury at the CGC 2023 Annual Meeting.
Explore genomic information's role in treating Myelodysplastic Syndrome (MDS). Gain insights into cutting-edge approaches for accurate diagnosis and personalized therapy in cancer genomics.
Explore WHO/IARC's collaboration with CGC, focusing on best practices in clinical cancer genomics and accurate diagnosis for targeted therapy.
Explore updates to ISCN 2024 and preview new genomic mapping nomenclature. Gain insights into evolving standards for clinical cancer genomics and their impact on patient care.
Explore the continued relevance of cytogenetics in modern genomics, highlighting its crucial role in cancer diagnosis and treatment strategies.
Explore challenges and recommendations for interpreting low penetrance variants and risk alleles in cancer genomics, improving harmonization across molecular diagnostics.
Explore standardized classification of oncogenic somatic variants in cancer, improving consistency through validated SOP and real-world case demonstrations.
Explore breast cancer genome heterogeneity, focusing on risk assessment and prevention strategies beyond therapy. Gain insights from expert Olufunmilayo Olopade at the CGC 2023 Annual Meeting.
Explore NPM1 mutations in myeloid malignancies and their impact on precision medicine through molecular testing. Gain insights from expert Robert Hasserjian on advancing cancer diagnostics and treatment.
Explore cutting-edge CAR-T therapies for T cell malignancies in this keynote presentation, focusing on advancements in cancer genomics and personalized treatment approaches.
Explore cutting-edge cancer genomics research, focusing on childhood brain tumors and ovarian cancer. Gain insights into copy number alterations, single-cell RNA sequencing, and their impact on patient outcomes.
Explore federated analysis for germline variant interpretation in cancer genomics, focusing on privacy-preserving data sharing techniques and overcoming challenges in workflow security and data standards.
Explore the intersection of pathology and bioinformatics in next-generation curating for cancer genomics. Gain insights into best practices and advancements in clinical cancer genomic testing.
Explore the relationship between genetic ancestry, somatic alterations, and cancer outcomes in this insightful presentation by Jian Carrot-Zhang at the 2022 CGC Annual Meeting.
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