Biology subjects

Azevedo, T.

Publications and source records attributed to Azevedo, T..

6 recordsLinked to original sources

bioRxiv2025

Uncertainty-Aware Tau Detection in Progressive Supranuclear Palsy Using Object Detection Models

Abnormal tau accumulation is a hallmark of neurodegenerative tauopathies such as Progressive Supranuclear Palsy (PSP). Traditional post-mortem assessments rely on manual lesion annotation, which is time-consuming and subjective. Existing machine learning methods typically involve multi-stage, feature-based pipelines, resulting in limited scalability and reliance on handcrafted features. This work evaluates deep learning-based object detection (OD) as a unified, end-to-end alternative for automating tau lesion identification and classification. We fine-tuned YOLO and Faster R-CNN models on a dataset of 29,852 tau lesions from 16 PSP brain slides, achieving mAP@50 of 0.702. To address the limitations of conventional OD models, which assume overconfident spatial predictions, we integrated Monte Carlo Dropout into both architectures to estimate spatial and label uncertainty. We evaluated detection uncertainty using Probability-based Detection Quality. Our results demonstrate that incorporating uncertainty offers a more comprehensive evaluation of detection reliability, complementing traditional metrics like mAP. For clinical application, we integrate a non-stochastic YOLO model into QuPath for whole-slide inference. Downstream clinical validation was conducted, including SHAP-based saliency analysis and correlation between model-predicted tau densities and PSP Rating Scale scores, a clinical disease severity measure. The alignment of detection outputs with pathological features and clinical severity underscores the clinical utility of OD models. Overall, this work highlights the complementary strengths of deep object detectors and uncertainty quantification, offering a path toward scalable, interpretable, and clinically meaningful tau pathology analysis. Code is available at https://github.com/Pidongg/dl_histopathology.

bioinformatics↗

bioRxiv2020

A Deep Graph Neural Network Architecture for Modelling Spatio-temporal Dynamics in resting-stating functional MRI Data

Resting-state functional magnetic resonance imaging (rs-fMRI) has been successfully employed to understand the organisation of the human brain. For rs-fMRI analysis, the brain is typically parcellated into regions of interest (ROIs) and modelled as a graph where each ROI is a node and pairwise correlation between ROI blood-oxygen-level-dependent (BOLD) time series are edges. Recently, graph neural networks (GNNs) have seen a surge in popularity due to their successes in modelling unstructured relational data. The latest developments with GNNs, however, have not yet been fully exploited for the analysis of rs-fMRI data, particularly with regards to its spatio-temporal dynamics. Herein we present a novel deep neural network architecture, combining both GNNs and temporal convolutional networks (TCNs), which is able to learn from the spatial and temporal components of rs-fMRI data in an end-to-end fashion. In particular, this corresponds to intra-feature learning (i.e., learning temporal dynamics with TCNs) as well as inter-feature learning (i.e., leveraging spatial interactions between ROIs with GNNs). We evaluate our model with an ablation study using 35,159 samples from the UK Biobank rs-fMRI database. We also demonstrate explainability features of our architecture which map to realistic neurobiological insights. We hope our model could lay the groundwork for future deep learning architectures focused on leveraging the inherently and inextricably spatio-temporal nature of rs-fMRI data.

neuroscience↗

bioRxiv2020

Population GNNs for Brain Age Prediction

Many common neurological and neurodegenerative disorders, such as Alzheimers disease, dementia and multiple sclerosis, have been associated with abnormal patterns of apparent ageing of the brain. Discrepancies between the estimated brain age and the actual chronological age (brain age gaps) can be used to understand the biological pathways behind the ageing process, assess an individuals risk for various brain disorders and identify new personalised treatment strategies. By flexibly integrating minimally preprocessed neuroimaging and non-imaging modalities into a population graph data structure, we train two types of graph neural network (GNN) architectures to predict brain age in a clinically relevant fashion as well as investigate their robustness to noisy inputs and graph sparsity. The multimodal population graph approach has the potential to learn from the entire cohort of healthy and affected subjects of both sexes at once, capturing a wide range of con-founding effects and detecting variations in brain age trends between different sub-populations of subjects.

neuroscience↗

bioRxiv2020

Gene Expression Imputation with Generative Adversarial Imputation Nets

A question of fundamental biological significance is to what extent the expression of a subset of genes can be used to recover the full transcriptome, with important implications for biological discovery and clinical application. To address this challenge, we present GAIN-GTEx, a method for gene expression imputation based on Generative Adversarial Imputation Networks. In order to increase the applicability of our approach, we leverage data from GTEx v8, a reference resource that has generated a comprehensive collection of transcriptomes from a diverse set of human tissues. We compare our model to several standard and state-of-the-art imputation methods and show that GAIN-GTEx is significantly superior in terms of predictive performance and runtime. Furthermore, our results indicate strong generalisation on RNA-Seq data from 3 cancer types across varying levels of missingness. Our work can facilitate a cost-effective integration of large-scale RNA biorepositories into genomic studies of disease, with high applicability across diverse tissue types.

bioinformatics↗

bioRxiv2020

Multilayer modelling and analysis of the humantranscriptome

Here, we performed a comprehensive intra-tissue and inter-tissue network analysis of the human transcriptome. We generated an atlas of communities in co-expression networks in 49 tissues (GTEx v8), evaluated their tissue specificity, and investigated their methodological implications. UMAP embeddings of gene expression from the communities (representing nearly 18% of all genes) robustly identified biologically-meaningful clusters. Methodologically, integration of the communities into a transcriptome-wide association study of C-reactive protein (CRP) in 361,194 individuals in the UK Biobank identified genetically-determined expression changes associated with CRP and led to considerably improved performance. Furthermore, a deep learning framework applied to the communities in nearly 11,000 tumours profiled by The Cancer Genome Atlas across 33 different cancer types learned biologically-meaningful latent spaces, representing metastasis (p < 2.2 x 10-16) and stemness (p < 2.2 x 10-16). Our study provides a rich genomic resource to catalyse research into inter-tissue regulatory mechanisms and their downstream phenotypic consequences.

genomics↗

bioRxiv2019

A machine learning tool for interpreting differences in cognition using brain features

Predicting variability in cognition traits is an attractive and challenging area of research, where different approaches and datasets have been implemented with mixed results. Some powerful Machine Learning algorithms employed before are difficult to interpret, while other algorithms are easy to interpret but might not be as powerful. To improve understanding of individual cognitive differences in humans, we make use of the most recent developments in Machine Learning in which powerful prediction models can be interpreted with confidence. We used neuroimaging data and a variety of behavioural, cognitive, affective and health measures from 905 people obtained from the Human Connectome Project (HCP). As a main contribution of this paper, we show how one could interpret the neuroanatomical basis of cognition, with recent methods which we believe are not yet fully explored in the field. By reducing neuroimages to a well characterised set of features generated from surface-based morphometry and cortical myelin estimates, we make the interpretation of such models easier as each feature is self-explanatory. The code used in this tool is available in a public repository: https://github.com/tjiagoM/interpreting-cognition-paper-2019

neuroscience↗