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January 18, 2026eLife2 citationsOpen Access

Biologically informed cortical models predict optogenetic perturbations

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CSChristos SourmpisHuawei Technologies (United Kingdom)CPCarl CH PetersenÉcole Polytechnique Fédérale de LausanneWGW Gerstner

Key Points

  • The aim is to enhance RNNs to better predict neural responses to optogenetic perturbations using biological principles.
  • Fitted recurrent neural networks to large electrophysiological datasets
  • Tested networks on unseen optogenetic interventions
  • Incorporated biological inductive biases such as structured connectivity and spiking dynamics
  • Generic RNNs displayed poor generalization on optogenetic perturbations
  • Biologically informed RNNs improved prediction accuracy on perturbed trials
  • Demonstrated utility in real-time targeting of micro-perturbations to influence behavior

Abstract

A recurrent neural network fitted to large electrophysiological datasets may help us understand the chain of cortical information transmission. In particular, successful network reconstruction methods should enable a model to predict the response to optogenetic perturbations. We test recurrent neural networks (RNNs) fitted to electrophysiological datasets on unseen optogenetic interventions and measure that generic RNNs used predominantly in the field generalize poorly on these perturbations. Our alternative RNN model adds biologically informed inductive biases like structured connectivity of excitatory and inhibitory neurons and spiking neuron dynamics. We measure that some biological inductive biases improve the model prediction on perturbed trials in a simulated dataset and a dataset recorded in mice in vivo. Furthermore, we show in theory and simulations that gradients of the fitted RNN can be used to target micro-perturbations in the recorded circuits and discuss the potential utility to bias an animal’s behavior and study cortical circuit mechanisms.

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Cite This Study

Sourmpis et al. (2026) studied this question.

synapsesocial.com/papers/696c7835eb60fb80d1396799https://doi.org/10.7554/elife.106827.3
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