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• W4290769203 abstract "Which cell types constitute brain circuits is a fundamental question, but establishing the correspondence across cellular data modalities is challenging. Bio-realistic models allow probing cause-and-effect and linking seemingly disparate modalities. Here, we introduce a computational optimization workflow to generate 9,200 single-neuron models with active conductances. These models are based on 230 in vitro electrophysiological experiments followed by morphological reconstruction from the mouse visual cortex. We show that, in contrast to current belief, the generated models are robust representations of individual experiments and cortical cell types as defined via cellular electrophysiology or transcriptomics. Next, we show that differences in specific conductances predicted from the models reflect differences in gene expression supported by single-cell transcriptomics. The differences in model conductances, in turn, explain electrophysiological differences observed between the cortical subclasses. Our computational effort reconciles single-cell modalities that define cell types and enables causal relationships to be examined." @default.
• W4290769203 created "2022-08-09" @default.
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• W4290769203 date "2022-08-01" @default.
• W4290769203 modified "2023-10-15" @default.
• W4290769203 title "Single-neuron models linking electrophysiology, morphology, and transcriptomics across cortical cell types" @default.
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• W4290769203 doi "https://doi.org/10.1016/j.celrep.2022.111176" @default.
• W4290769203 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/35947954" @default.
• W4290769203 hasPublicationYear "2022" @default.
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