
Morphology & Electrophysiology: Instantly explore brain regions, morphologies, hierarchical cell types (M-types), and electrophysiological recordings in an interactive 3D atlas.
Models & Simulations: Access validated multiscale computational models — from ion channels to neurons and circuits — plus whole-cell patch clamp recordings across species, including human cortical tissue. Run Python analyses to generate real-time metrics and visualizations.
AI Literature Mining: Search neuroscience papers, extract simulation protocols, and summarize findings using natural-language queries powered by OBI-ONE.
Smart Data Analysis: Compute morphometric, electrophysiological, and circuit-level metrics, estimate connection probabilities, and visualize results interactively.
Create data-based genetic ion channels to use in single cell models.
Study genetic ion channel dynamics.
Study the effect of channel parameters on the model currents.
Compare firing properties across diverse cell types and brain regions.
Study the role of specific ionic currents in shaping action potentials.
Investigate dendritic computation and action potential backpropagation.
Analyze the effects of synapse activation patterns on single-neuron responses.
Investigate how proximal and distal inhibition modulates somatic action potentials.
Systematically vary synaptic parameters to characterize integration properties and plasticity rules.
Build your knowledge - recreate classic neuroscience results.
Test your understanding – can you predict a network’s activity from the input you provide.
Test the effect of different inhibitory populations on spiking activity.
Use the pre-installed packages to write your own analyses and share them with your team.
Share the results of your research with the world.
Learn about platform features and how to work with the data, models and simulations on the platform through OBI-curated instructional notebooks.
Develop your own instructional notebooks and share them with your students for classes and teaching.
Use notebook templates to evaluate your students’ progress.
Reconstruct high-quality, smooth neuronal morphologies from dense EM data, including highly tessellated, fragmented mesh, or volumetric models, using efficient skeletonization algorithms.
Segment somata to generate accurate mesh and volumetric models ready for quantitative analysis.
Segment dendritic spines and build high-resolution spine meshes with clean, biologically consistent geometric topology.
Skeletonize dendritic spines to produce detailed morphological skeletons for advanced structural studies.
Generate high-quality, watertight neuronal mesh models from fragmented inputs, fully compatible with reaction–diffusion simulations.