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Larissa Höfling

Publications and source records attributed to Larissa Höfling.

2 recordsLinked to original sources

Only Brains Align with Brains: Cross-Region Alignment Patterns Expose Limits of Normative Models

Neuroscientists and computer vision researchers use model-brain alignment benchmarks to compare artificial and biological vision systems. These benchmarks rank models according to alignment measures such as the similarity of representational geometry or the predictability of neural responses from model activations. However, recent works have identified a number of problems with these rankings, among them their lack of discriminative power and robustness, raising the conceptual question of what it means for a model to be brain-aligned. Here we introduce alignment patterns -- characteristic functional relationship profiles of each brain region to all others -- and propose that models should reproduce these patterns to qualify as brain-aligned. First, we apply a standard benchmarking pipeline to a broad spectrum of vision models of the BOLD Moments video fMRI dataset across visual regions of interest (ROIs). We find diverse models appear equivalent in their brain alignment, reflecting the lack of discriminative power of conventional alignment benchmarking pipelines. In contrast, alignment pattern analysis (APA) is a second-order structural consistency test: a model aligned to a given ROI should reproduce that ROI's characteristic cross-region alignment profile. Applying APA, we find that, while these patterns are highly stable across brains of different subjects, even top-ranked models often fail to capture them. Finally, we argue for a clearer distinction between the criteria a model must meet to serve as a tool versus as a computational model for human visual cortex. Conventional alignment measures may be sufficient for identifying neurally predictive models, but claims about computational or algorithmic similarity may require a stronger basis of evidence, including the reproducibility of relational alignment patterns.

q-bio.NC↗

Most discriminative stimuli for functional cell type clustering

Identifying cell types and understanding their functional properties is crucial for unraveling the mechanisms underlying perception and cognition. In the retina, functional types can be identified by carefully selected stimuli, but this requires expert domain knowledge and biases the procedure towards previously known cell types. In the visual cortex, it is still unknown what functional types exist and how to identify them. Thus, for unbiased identification of the functional cell types in retina and visual cortex, new approaches are needed. Here we propose an optimization-based clustering approach using deep predictive models to obtain functional clusters of neurons using Most Discriminative Stimuli (MDS). Our approach alternates between stimulus optimization with cluster reassignment akin to an expectation-maximization algorithm. The algorithm recovers functional clusters in mouse retina, marmoset retina and macaque visual area V4. This demonstrates that our approach can successfully find discriminative stimuli across species, stages of the visual system and recording techniques. The resulting most discriminative stimuli can be used to assign functional cell types fast and on the fly, without the need to train complex predictive models or show a large natural scene dataset, paving the way for experiments that were previously limited by experimental time. Crucially, MDS are interpretable: they visualize the distinctive stimulus patterns that most unambiguously identify a specific type of neuron.

q-bio.NC↗