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Senanayake, D.

Publications and source records attributed to Senanayake, D..

2 recordsLinked to original sources

Knowledge Inclusive Machine Learning for Disease Gene Prioritisation

The predictive performance of machine learning models depends on the context available to them. In disease gene prioritisation, this context comprises two forms: specific context from sample-level experimental data, such as gene expression and protein-protein interaction networks, and general context from accumulated and curated biological knowledge capturing established relationships among genes, diseases, and pathways. Neither is sufficient alone: experimental data are sensitive to dataset-specific noise and lack broader biological grounding, while curated knowledge lacks the resolution required for gene-level discrimination. Consequently, most machine learning approaches relying solely on experimental data risk learning spurious correlations rather than underlying biology. Here we introduce Knowledge Inclusive Machine Learning (KIML), a paradigm that integrates both context types within a unified analytical pipeline. KIML combines experimental data with two types of general context: literature-derived representations from PubMed and structured biomedical knowledge graphs. We evaluate the approach on Developmental and Epileptic Encephalopathy and benchmark it against recent methods using publicly available datasets. Performance is assessed using temporal-split evaluation and biological evaluations, including ontology enrichment analysis. KIML consistently outperforms existing approaches, providing improved predictive accuracy and biologically meaningful insights. Furthermore, the framework generates interpretable explanations of gene prioritisation and demonstrates strong generalisability across six additional diseases.

genetics↗

Visualization of Incrementally Learned Projection Trajectories for Longitudinal Data

Longitudinal studies that continuously generate data enable the capture of temporal variations in experimentally observed parameters, facilitating the interpretation of results in a time-aware manner. We propose IL-VIS (Incrementally Learned Visualizer), a new machine learning pipeline that incrementally learns and visualizes a progression trajectory representing the longitudinal changes in longitudinal studies. At each sampling time point in an experiment, IL-VIS generates a snapshot of the longitudinal process on the data observed thus far, a new feature that is beyond the reach of classical static models. We first verify the utility and correctness of IL-VIS using simulated data, for which the true progression trajectories are known. We find that it accurately captures and visualizes the trends and (dis)similarities between high-dimensional progression trajectories. We then apply IL-VIS to longitudinal Multi-Electrode Array data from brain cortical organoids when exposed to different levels of Quinolinic Acid, a metabolite contributing to many neuroinflammatory diseases including Alzheimers disease, and its blocking antibody. We uncover valuable insights into the organoids electrophysiological maturation and response patterns over time under these conditions.

bioinformatics↗