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bioRxiv · 10.1101/2025.03.27.645646

Trial-Level Representational Similarity Analysis

Abstract

Neural representation refers to the brain activity that stands in for ones cognitive experience, and in cognitive neuroscience, a prominent method of studying neural representations is representational similarity analysis (RSA). While there are several recent advances in RSA, the classic RSA (cRSA) approach examines the structure of representations across numerous items by assessing the correspondence between two representational similarity matrices (RSMs): usually one based on a theoretical model of stimulus similarity and the other based on similarity in measured neural data. However, because cRSA cannot weigh the contributions of individual trials (RSM rows/columns), it is fundamentally limited in its ability to assess subject-, stimulus-, and trial-level variances that all influence representation. Here, we formally introduce trial-level RSA (tRSA), an analytical framework that estimates the strength of neural representation for singular experimental trials and evaluates hypotheses using multi-level models. First, we verified the correspondence between tRSA and cRSA in quantifying the overall representation strength across all trials. Second, we compared the statistical inferences drawn from both approaches using simulated data that reflected a wide range of scenarios. Compared to cRSA, the multi-level framework of tRSA was both more theoretically appropriate and significantly sensitive to true effects. Third, using real fMRI datasets, we further demonstrated several issues with cRSA, to which tRSA was more robust. Finally, we presented some novel findings of neural representations that could only be assessed with tRSA and not cRSA. In summary, tRSA proves to be a robust and versatile analytical approach for cognitive neuroscience and beyond.

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BibTeXRIS

Huang, S., Howard, C. M., Bogdan, P. C., Morales-Torres, R., Slayton, M., Cabeza, R., Davis, S. W.. 2025-04-01. Trial-Level Representational Similarity Analysis. https://doi.org/10.1101/2025.03.27.645646

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