Search bioRxiv⌕ Search

bioRxiv · 10.1101/2024.11.28.625854

More or less latent variables in the high-dimensional data space? That is the question

Abstract

Dimensionality reduction is widely used in modern Neuro-science to process massive neural recordings data. Despite the development of complex non-linear techniques, linear algorithms, in particular Principal Component Analysis (PCA), are still the gold standard. However, there is no consensus on how to estimate the optimal number of latent variables to retain. In this study, we addressed this issue by testing different criteria on simulated data. Parallel analysis and cross validation proved to be the best methods, being largely unaffected by the number of units and the amount of noise. Parallel analysis was quite conservative and tended to underestimate the number of dimensions especially in low-noise regimes, whereas in these conditions cross validation provided slightly better estimates. Both criteria consistently estimate the ground truth when 100+ units were available. As an exemplary application to real data, we estimated the dimensionality of the spiking activity in two macaque parietal areas during different phases of a delayed reaching task. We show that different criteria can lead to different trends in the estimated dimensionality. These apparently contrasting results are reconciled when the implicit definition of dimensionality underlying the different criteria is considered. Our findings suggest that the term dimensionality needs to be defined carefully and, more importantly, that the most robust criteria for choosing the number of dimensions should be adopted in future works. To help other researchers with the implementation of such an approach on their data, we provide a simple software package, and we present the results of our simulations through a simple Web based app to guide the choice of latent variables in a variety of new studies. Key pointsO_LIParallel analysis and cross-validation are the most effective criteria for principal components retention, with parallel analysis being slightly more conservative in low-noise conditions, but being more robust with larger noise. C_LIO_LIThe size of data matrix as well as the decay rate of the explained variance decreasing curve strongly limit the number of latent components that should be considered. C_LIO_LIWhen analyzing real spiking data, the estimated dimensionality depends dramatically on the criterion used, leading to apparently different results. However, these differences stem, in large part, from the implicit definitions of dimensionality underlying each criterion. C_LIO_LIThis study emphasizes the need for careful definition of dimensionality in population spiking activity and suggests the use of parallel analysis and cross-validation methods for future research. C_LI

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Vaccari, F. E., Diomedi, S., Bettazzi, E., Filippini, M., De Vitis, M., Hadjidimitrakis, K., Fattori, P.. 2024-11-28. More or less latent variables in the high-dimensional data space? That is the question. https://doi.org/10.1101/2024.11.28.625854

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related preprints

Functional validation of allele-specific LMNB1 silencing in patient-derived astrocytes as a therapeutic option for Autosomal Dominant Leukodystrophy

Adult-onset Autosomal Dominant Leukodystrophy (ADLD) is a rare fatal leukodystrophy caused by increased LMNB1 gene dosage, most commonly resulting from duplication of the LMNB1 locus. Because ADLD is a gene dosage disorder, selective reduction of pathological LMNB1 expression represents a rational therapeutic strategy. Although allele-specific RNA interference has previously been shown to lower LMNB1 levels in patient-derived fibroblasts and directly reprogrammed neurons, its therapeutic effects have not been evaluated in disease-relevant human glial cells or using functional efficacy endpoints. Here, we established human induced pluripotent stem cell-derived astrocytes from ADLD patients as a human glial model in which to validate allele-specific LMNB1 silencing across molecular, cellular, and functional readouts. ADLD astrocytes recapitulated increased LMNB1 expression and characteristic nuclear abnormalities and displayed transcriptional alterations affecting extracellular matrix organization, calcium homeostasis, metabolism and RNA processing. Functionally, these cells also exhibited functional phenotypes suitable for therapeutic evaluation: astrocyte-conditioned medium impaired the viability of both murine and human oligodendroglial cultures, while conditioned-medium and direct astrocyte-seeding paradigms revealed impaired post-lesion myelin recovery in lysolecithin-treated cerebellar organotypic slices. Allele-specific LMNB1 silencing restored physiological LMNB1 levels, corrected nuclear abnormalities, attenuated astrocyte-mediated oligodendroglial toxicity, improved post-lesion myelin recovery, and was associated with selective transcriptional programs associated with extracellular support and cholesterol metabolism. Together, these findings provide molecular, cellular, and functional validation of allele-specific LMNB1 dosage correction in patient-derived human astrocytes and offer key support for LMNB1-lowering strategies in disease-relevant human glial cells.

neuroscience↗

Perceptual integration of multisensory haptic, visual, and auditory feedback for roughness discrimination in augmented reality

Understanding how our different senses interact to shape our perception is essential to design realistic and immersive virtual and augmented reality (VR/AR) experiences. The present study investigated how roughness perception can be modulated through haptic, visual, and auditory cues in AR using a vibrotactile wristband. Participants compared virtual textures varying in vibration frequency/amplitude, visual grain size, and friction sound. Results revealed strong linear relationships between stimulus parameters and perceived roughness, with haptic frequency and visual cues driving the highest discrimination performance. Adding non-informative sensory feedback reduced perceptual sensitivity, acting as noise. Individual differences emerged: participants who rated haptic as the easiest modality showed greater sensitivity to haptic variations, while visual-reliant participants performed better with visual cues. We conclude that roughness in AR can be systematically manipulated, but is vulnerable to perceptual interference from irrelevant inputs, where our work provides actionable insights for implementing optimized and adaptive AR/VR interfaces.

neuroscience↗

Structural and functional MRI signatures of Gambling Disorder: a case-control study

Gambling disorder (GD) is a behavioural addiction that may help identify addiction-related neural features without the direct neurobiological effects of a primary substance of dependence. We examined regional grey matter volume (GMV) and resting-state functional connectivity (rsFC) in the same well-characterised sample. Eighteen men with GD and 21 matched healthy controls underwent high-resolution structural and resting-state functional MRI. GMV was quantified across 214 cortical and subcortical regions, and seed-based rsFC analyses focused on striatal subdivisions and mesocorticolimbic regions. Group differences were evaluated using permutation testing and cluster-corrected mixed-effects modelling. GD was associated with lower GMV in the ventromedial prefrontal cortex, orbitofrontal regions and other cortical and subcortical areas, alongside higher GMV in a subset of limbic and default-mode regions. Participants with GD also showed lower connectivity between the limbic striatum and the hippocampus, thalamus and putamen. In exploratory analyses, somatomotor connectivity was positively associated with gambling severity (Problem Gambling Severity Index: Spearman's rho = 0.71, p = 0.003, false-discovery-rate-adjusted q = 0.016). Structural and functional findings overlapped spatially in regions associated with valuation, memory, reward and habit formation, but regional GMV did not mediate group differences in rsFC. These findings are broadly consistent with corticostriatal models of GD and identify candidate circuit-level differences for independent replication. Larger, more diverse and longitudinal samples are required to establish their reproducibility, temporal direction and clinical relevance.

neuroscience↗