Search bioRxiv⌕ Search

bioRxiv · 10.64898/2026.09.01.748559

DRUMS - A Flexible New Deep Learning Tool for Precise Cortical Surface Alignment across Individuals

Abstract

Accurate inter-individual alignment of human cerebral cortex is challenging because of the high variability of human cortical folding patterns and the regionally non-uniform and inconsistent spatial relationships across individuals of cortical folds versus the functional networks and cortical areas that we wish to study. To achieve precise alignment across individuals, an algorithm must use multi-modal neuroimaging features related to cortical areas and functional networks, ideally as inputs to surface-based registration, but at least during training if only folding patterns will be available during inference, so that it can learn where folding patterns are trustworthy and learn a spatially non-uniform regularization function that reflects the true gamut of human inter-individual variability in cortical organization. Additionally, an algorithm ideally will be capable of denoising its own input registration features to avoid overfitting to noise, enabling reproducible registration in test-retest data, and will not require precise hand tuning of input regularization parameters. To address these challenges, we developed Deep-learning Registration Using U-Net with Multimodal Supervision (DRUMS), a novel framework for multi-modal cortical surface registration. DRUMS applies its deep-learning approach to cortical surface registration using multi-resolution spheres, a well-validated approach used in other registration algorithms such as Multi-modal Surface Matching (MSM) (Robinson, et al., 2014; Robinson, et al., 2018). It also includes the same physically inspired strain energy regularization that we pioneered for MSM and the same precise barycentric interpolation on spherical surface meshes. DRUMS has a three-stage architecture: (1) multiscale feature extraction, (2) multiscale feature integration, and (3) deformation field generation. The framework's multimodal design supports flexible integration of diverse imaging modalities, enabling registration using either folding features or multi-modal features as inputs with independent control over supervision during training (e.g., training DRUMS with folding inputs and multi-modal supervision to learn which folds best correlate with multi-modal features). DRUMS outperforms Multi-modal Surface Matching (MSM), the current state-of-the-art method used in the Human Connectome Project (HCP) pipelines, over a wide range of input regularization settings in both registration accuracy and test-retest reproducibility of registration results for both supervised folding registrations and multi-modal registrations across all tested modalities, including held out modalities. DRUMS further learns a biologically plausible spatially non-uniform regularization function, with registration induced distortion correctly matched to known human inter-individual cortical variability. These results suggest that DRUMS should replace MSM in the HCP Pipelines and position DRUMS as a versatile and reliable tool for cortical surface registration in neuroimaging research.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Wang, Y., Coalson, T. S., Yang, C., Van Essen, D. C., Glasser, M. F.. 2026-09-06. DRUMS - A Flexible New Deep Learning Tool for Precise Cortical Surface Alignment across Individuals. https://doi.org/10.64898/2026.09.01.748559

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↗