In this paper we introduce SynaptoGen, a novel framework that aims to bridge the gap between genetic manipulations and neuronal network behavior by simulating synaptogenesis and guiding the development of neuronal networks capable of solving predetermined computational tasks. Drawing inspiration from recent advancements in the field, we propose SynaptoGen as a bio-plausible approach to modeling synaptogenesis through differentiable functions. To validate SynaptoGen, we conduct a preliminary experiment using reinforcement learning as a benchmark learning framework, demonstrating its effectiveness in generating neuronal networks capable of solving the OpenAI Gym's Cart Pole task, compared to carefully designed baselines. The results highlight the potential of SynaptoGen to inspire further advancements in neuroscience and computational modeling, while also acknowledging the need for incorporating more realistic genetic rules and synaptic conductances in future research. Overall, SynaptoGen represents a promising avenue for exploring the intersection of genetics, neuroscience, and artificial intelligence.
Decoding visual representations from human brain activity has emerged as a thriving research domain, particularly in the context of brain-computer interfaces. Our study presents an innovative method that employs to classify and reconstruct images from the ImageNet dataset using electroencephalography (EEG) data from subjects that had viewed the images themselves (i.e. "brain decoding"). We analyzed EEG recordings from 6 participants, each exposed to 50 images spanning 40 unique semantic categories. These EEG readings were converted into spectrograms, which were then used to train a convolutional neural network (CNN), integrated with a knowledge distillation procedure based on a pre-trained Contrastive Language-Image Pre-Training (CLIP)-based image classification teacher network. This strategy allowed our model to attain a top-5 accuracy of 80%, significantly outperforming a standard CNN and various RNN-based benchmarks. Additionally, we incorporated an image reconstruction mechanism based on pre-trained latent diffusion models, which allowed us to generate an estimate of the images which had elicited EEG activity. Therefore, our architecture not only decodes images from neural activity but also offers a credible image reconstruction from EEG only, paving the way for e.g. swift, individualized feedback experiments. Our research represents a significant step forward in connecting neural signals with visual cognition.
Every day, the human brain processes an immense volume of visual information, relying on intricate neural mechanisms to perceive and interpret these stimuli. Recent breakthroughs in functional magnetic resonance imaging (fMRI) have enabled scientists to extract visual information from human brain activity patterns. In this study, we present an innovative method for decoding brain activity into meaningful images and captions, with a specific focus on brain captioning due to its enhanced flexibility as compared to brain decoding into images. Our approach takes advantage of cutting-edge image captioning models and incorporates a unique image reconstruction pipeline that utilizes latent diffusion models and depth estimation. We utilized the Natural Scenes Dataset, a comprehensive fMRI dataset from eight subjects who viewed images from the COCO dataset. We employed the Generative Image-to-text Transformer (GIT) as our backbone for captioning and propose a new image reconstruction pipeline based on latent diffusion models. The method involves training regularized linear regression models between brain activity and extracted features. Additionally, we incorporated depth maps from the ControlNet model to further guide the reconstruction process. We evaluate our methods using quantitative metrics for both generated captions and images. Our brain captioning approach outperforms existing methods, while our image reconstruction pipeline generates plausible images with improved spatial relationships. In conclusion, we demonstrate significant progress in brain decoding, showcasing the enormous potential of integrating vision and language to better understand human cognition. Our approach provides a flexible platform for future research, with potential applications in various fields, including neural art, style transfer, and portable devices.
In this study, we explore the impact of network topology on the approximation capabilities of artificial neural networks (ANNs), with a particular focus on complex topologies. We propose a novel methodology for constructing complex ANNs based on various topologies, including Barab\'asi-Albert, Erd\H{o}s-R\'enyi, Watts-Strogatz, and multilayer perceptrons (MLPs). The constructed networks are evaluated on synthetic datasets generated from manifold learning generators, with varying levels of task difficulty and noise. Our findings reveal that complex topologies lead to superior performance in high-difficulty regimes compared to traditional MLPs. This performance advantage is attributed to the ability of complex networks to exploit the compositionality of the underlying target function. However, this benefit comes at the cost of increased forward-pass computation time and reduced robustness to graph damage. Additionally, we investigate the relationship between various topological attributes and model performance. Our analysis shows that no single attribute can account for the observed performance differences, suggesting that the influence of network topology on approximation capabilities may be more intricate than a simple correlation with individual topological attributes. Our study sheds light on the potential of complex topologies for enhancing the performance of ANNs and provides a foundation for future research exploring the interplay between multiple topological attributes and their impact on model performance.
Recently, it has become progressively more evident that classic diagnostic labels are unable to reliably describe the complexity and variability of several clinical phenotypes. This is particularly true for a broad range of neuropsychiatric illnesses (e.g., depression, anxiety disorders, behavioral phenotypes). Patient heterogeneity can be better described by grouping individuals into novel categories based on empirically derived sections of intersecting continua that span across and beyond traditional categorical borders. In this context, neuroimaging data carry a wealth of spatiotemporally resolved information about each patient's brain. However, they are usually heavily collapsed a priori through procedures which are not learned as part of model training, and consequently not optimized for the downstream prediction task. This is because every individual participant usually comes with multiple whole-brain 3D imaging modalities often accompanied by a deep genotypic and phenotypic characterization, hence posing formidable computational challenges. In this paper we design a deep learning architecture based on generative models rooted in a modular approach and separable convolutional blocks to a) fuse multiple 3D neuroimaging modalities on a voxel-wise level, b) convert them into informative latent embeddings through heavy dimensionality reduction, c) maintain good generalizability and minimal information loss. As proof of concept, we test our architecture on the well characterized Human Connectome Project database demonstrating that our latent embeddings can be clustered into easily separable subject strata which, in turn, map to different phenotypical information which was not included in the embedding creation process. This may be of aid in predicting disease evolution as well as drug response, hence supporting mechanistic disease understanding and empowering clinical trials.
Graphs are a natural representation of brain activity derived from functional magnetic imaging (fMRI) data. It is well known that clusters of anatomical brain regions, known as functional connectivity networks (FCNs), encode temporal relationships which can serve as useful biomarkers for understanding brain function and dysfunction. Previous works, however, ignore the temporal dynamics of the brain and focus on static graphs. In this paper, we propose a dynamic brain graph deep generative model (DBGDGM) which simultaneously clusters brain regions into temporally evolving communities and learns dynamic unsupervised node embeddings. Specifically, DBGDGM represents brain graph nodes as embeddings sampled from a distribution over communities that evolve over time. We parameterise this community distribution using neural networks that learn from subject and node embeddings as well as past community assignments. Experiments demonstrate DBGDGM outperforms baselines in graph generation, dynamic link prediction, and is comparable for graph classification. Finally, an analysis of the learnt community distributions reveals overlap with known FCNs reported in neuroscience literature.
Brain decoding is a field of computational neuroscience that uses measurable brain activity to infer mental states or internal representations of perceptual inputs. Therefore, we propose a novel approach to brain decoding that also relies on semantic and contextual similarity. We employ an fMRI dataset of natural image vision and create a deep learning decoding pipeline inspired by the existence of both bottom-up and top-down processes in human vision. We train a linear brain-to-feature model to map fMRI activity features to visual stimuli features, assuming that the brain projects visual information onto a space that is homeomorphic to the latent space represented by the last convolutional layer of a pretrained convolutional neural network, which typically collects a variety of semantic features that summarize and highlight similarities and differences between concepts. These features are then categorized in the latent space using a nearest-neighbor strategy, and the results are used to condition a generative latent diffusion model to create novel images. From fMRI data only, we produce reconstructions of visual stimuli that match the original content very well on a semantic level, surpassing the state of the art in previous literature. We evaluate our work and obtain good results using a quantitative semantic metric (the Wu-Palmer similarity metric over the WordNet lexicon, which had an average value of 0.57) and perform a human evaluation experiment that resulted in correct evaluation, according to the multiplicity of human criteria in evaluating image similarity, in over 80% of the test set.
Functional connectivity (FC) between regions of the brain is commonly estimated through statistical dependency measures applied to functional magnetic resonance imaging (fMRI) data. The resulting functional connectivity matrix (FCM) is often taken to represent the adjacency matrix of a brain graph. Recently, graph neural networks (GNNs) have been successfully applied to FCMs to learn brain graph representations. A common limitation of existing GNN approaches, however, is that they require the graph adjacency matrix to be known prior to model training. As such, it is implicitly assumed the ground-truth dependency structure of the data is known. Unfortunately, for fMRI this is not the case as the choice of which statistical measure best represents the dependency structure of the data is non-trivial. Also, most GNN applications to fMRI assume FC is static over time, which is at odds with neuroscientific evidence that functional brain networks are time-varying and dynamic. These compounded issues can have a detrimental effect on the capacity of GNNs to learn representations of brain graphs. As a solution, we propose Dynamic Brain Graph Structure Learning (DBGSL), a supervised method for learning the optimal time-varying dependency structure of fMRI data. Specifically, DBGSL learns a dynamic graph from fMRI timeseries via spatial-temporal attention applied to brain region embeddings. The resulting graph is then fed to a spatial-temporal GNN to learn a graph representation for classification. Experiments on large resting-state as well as task fMRI datasets for the task of gender classification demonstrate that DBGSL achieves state-of-the-art performance. Moreover, analysis of the learnt dynamic graphs highlights prediction-related brain regions which align with findings from existing neuroscience literature.
The willingness to trust predictions formulated by automatic algorithms is key in a vast number of domains. However, a vast number of deep architectures are only able to formulate predictions without an associated uncertainty. In this paper, we propose a method to convert a standard neural network into a Bayesian neural network and estimate the variability of predictions by sampling different networks similar to the original one at each forward pass. We couple our methods with a tunable rejection-based approach that employs only the fraction of the dataset that the model is able to classify with an uncertainty below a user-set threshold. We test our model in a large cohort of brain images from Alzheimer's Disease patients, where we tackle discrimination of patients from healthy controls based on morphometric images only. We demonstrate how combining the estimated uncertainty with a rejection-based approach increases classification accuracy from 0.86 to 0.95 while retaining 75% of the test set. In addition, the model can select cases to be recommended for manual evaluation based on excessive uncertainty. We believe that being able to estimate the uncertainty of a prediction, along with tools that can modulate the behavior of the network to a degree of confidence that the user is informed about (and comfortable with) can represent a crucial step in the direction of user compliance and easier integration of deep learning tools into everyday tasks currently performed by human operators.
In medicine, curated image datasets often employ discrete labels to describe what is known to be a continuous spectrum of healthy to pathological conditions, such as e.g. the Alzheimer's Disease Continuum or other areas where the image plays a pivotal point in diagnosis. We propose an architecture for image stratification based on a conditional variational autoencoder. Our framework, VAESim, leverages a continuous latent space to represent the continuum of disorders and finds clusters during training, which can then be used for image/patient stratification. The core of the method learns a set of prototypical vectors, each associated with a cluster. First, we perform a soft assignment of each data sample to the clusters. Then, we reconstruct the sample based on a similarity measure between the sample embedding and the prototypical vectors of the clusters. To update the prototypical embeddings, we use an exponential moving average of the most similar representations between actual prototypes and samples in the batch size. We test our approach on the MNIST-handwritten digit dataset and on a medical benchmark dataset called PneumoniaMNIST. We demonstrate that our method outperforms baselines in terms of kNN accuracy measured on a classification task against a standard VAE (up to 15% improvement in performance) in both datasets, and also performs at par with classification models trained in a fully supervised way. We also demonstrate how our model outperforms current, end-to-end models for unsupervised stratification.