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Explore ethical considerations in using population descriptors for genomic research. Learn from experts about the importance of thoughtful group categorization in science and society.
Explore natural sequencing-by-synthesis for scRNA-seq using Ultima sequencing. Learn about experiment design, data quality, analysis techniques, and biological insights in single-cell genomics.
Explore groundbreaking research by emerging scientists on neurodegenerative diseases, cardiac health, infectious disease diagnosis, and rare genetic disorders.
Explore mass spectrometry-based proteomics techniques for biomarker discovery and pQTL mapping in this workshop by Lili Niu from the University of Copenhagen.
Explore deep learning models for integrating patient-level multi-omics data, focusing on supervised and unsupervised approaches for predicting outcomes and uncovering latent representations in genomics.
Explore deep learning techniques for genomic discovery, focusing on high-resolution assays, footprint shapes, and bias correction methods in neural networks.
Explore Mendelian randomization's evolution, from its genetic roots to modern applications in epidemiology. Gain insights into its capabilities, limitations, and potential future developments in phenotypic causation research.
Explore spatial copy number alteration detection in Slide-seq-like spatial transcriptomics data. Learn basic genetics principles related to human populations and disease.
Explore Type 2 diabetes prevalence in Latino populations with Dr. Jose Florez's insightful presentation on genetic and environmental factors.
Explore the mechanism of protein antibiotics through the study of bacteriophage lysis proteins, focusing on Protein E's inhibition of MraY and its implications for novel therapeutic development.
Explore challenges in training infinitely large neural networks with Mikhail Belkin. Gain insights into foundational advances in machine learning for biomedical applications.
Explore challenges in evaluating FDA-approved medical AI devices and learn from a pioneering clinical trial assessing an AI for cardiac conditions.
Explore TACIT, a toolkit for relating enhancer genetic variation to complex phenotypes. Learn about tissue-aware conservation inference and its applications in medical and population genetics.
Explore cell death modulation for disease treatment with Amanda Ouchida in the René Salazar Speaker Series at Broad Institute.
Explore cutting-edge machine learning techniques for inferring single-cell profiles from histology images and generating omics data from various imaging modalities, bridging the gap between imaging and genomics.
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