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Explore Max Welling's insights on materials research through generation, emulation, and simulation techniques in this MIT-Harvard colloquium on machine learning applications in biomedical research.
Discover how homomorphic encryption enables ultra-secure genomic computations on encrypted data without exposing sensitive information, addressing privacy concerns in large-scale biobanks.
Discover how gene perturbations affect adipocytes in this machine learning challenge tackling obesity and metabolic diseases using CRISPR/Cas9 data.
Discover Biomni, a general-purpose biomedical AI agent that autonomously executes research tasks across gene prioritization, drug discovery, and clinical analysis using LLM reasoning and code execution.
Explore foundation models in biomedicine, from tissue-level modeling to comprehensive biological systems for advancing drug discovery through machine learning applications.
Explore AF2BIND, a novel approach using AlphaFold2 features to predict protein binding sites for drug discovery, plus deep learning embeddings for protein design.
Discover how genetic variants serve as natural experiments to infer causal relationships between traits and diseases in this genetics primer on Mendelian randomization methods.
Explore experimental data design for predicting CRISPR gene perturbation effects on adipocyte cell fate in obesity research using machine learning techniques.
Explore cutting-edge techniques for measuring gene expression in cells, focusing on CRISPR/Cas9 perturbations and adipocyte biology for obesity research applications.
Explore gene expression programs and CRISPR/Cas9 technology for predicting adipocyte fate in obesity research through machine learning techniques.
Explore how genomic medicine and precision healthcare technologies could transform medical care throughout your life with insights from Broad Institute scientist Niall Lennon.
Explore the Genomics 2 Proteins Portal through expert insights from the Iqbal Lab, covering essential tools and methods for translating genomic data into protein-level understanding.
Discover advanced permutation-based methods scDEED and mcRigor that enhance reliability in single-cell genomics data analysis, improving visualization accuracy and metacell partitioning.
Explore causal validity in machine learning for drug discovery and health monitoring, moving beyond prediction to establish causality in therapeutic target discovery and glucose dynamics modeling.
Explore cutting-edge deep learning methods for designing genomic edits and predicting transcription factor binding in regulatory genomics research.
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