Canonical template tracking: Measuring the activation state of specific neural representations

Front Neuroimaging. 2023 Jan 9:1:974927. doi: 10.3389/fnimg.2022.974927. eCollection 2022.

Abstract

Multivariate analyses of neural data have become increasingly influential in cognitive neuroscience since they allow to address questions about the representational signatures of neurocognitive phenomena. Here, we describe Canonical Template Tracking: a multivariate approach that employs independent localizer tasks to assess the activation state of specific representations during the execution of cognitive paradigms. We illustrate the benefits of this methodology in characterizing the particular content and format of task-induced representations, comparing it with standard (cross-)decoding and representational similarity analyses. Then, we discuss relevant design decisions for experiments using this analysis approach, focusing on the nature of the localizer tasks from which the canonical templates are derived. We further provide a step-by-step tutorial of this method, stressing the relevant analysis choices for functional magnetic resonance imaging and magneto/electroencephalography data. Importantly, we point out the potential pitfalls linked to canonical template tracking implementation and interpretation of the results, together with recommendations to mitigate them. To conclude, we provide some examples from previous literature that highlight the potential of this analysis to address relevant theoretical questions in cognitive neuroscience.

Keywords: EEG; canonical template; fMRI; multivariate analyses; neural representation.

Publication types

  • Review

Grants and funding

AP was funded by the Andalusian Autonomic Government (Grant Ref.: PAIDI 21_00207). SF was funded by the German Research Foundation (Deutsche Forschungsgemeinschaft, DFG) under Germany's Excellence Strategy-EXC 2002/1, Science of Intelligence (Project Ref.: 390523135) and the Einstein Foundation Berlin. MS was supported by a European Union's Horizon 2020 research and innovation program, Grant agreement 852570, and by Grant BOF17-GOA-004 from the Research Council of Ghent University. CG-G was supported by Grant IJC2019-040208-I and Project PID2020-116342GA-I00 funded by MCIN/AEI/10.13039/501100011033, and Grant RYC2021-033536-I funded by MCIN/AEI/10.13039/501100011033 and by the European Union NextGenerationEU/PRTR.