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Nilsson, S.

Publications and source records attributed to Nilsson, S..

3 recordsLinked to original sources

Community-aware explanations in knowledge graphs with XP-GNN

Machine learning applications for the drug discovery pipeline have exponentially increased in the last few years. An example of these applications is the biological Knowledge Graph. These graphs represent biological entities and the relations between them based on existing knowledge. Graph machine learning models such as Graph Neural Networks can be applied on top of knowledge graphs to support the development of novel therapeutics. Nevertheless, Graph Neural Networks present an improved performance at the expense of complexity, becoming difficult to explain their decisions. State-of-the-art explanation algorithms for Graph Neural Networks focus on determining the most relevant subgraphs involved in their decision-making while considering graph elements (nodes and edges) as independent entities and ignoring any communities these graphs could present. We explore in this work the idea that graph community structure in biological Knowledge Graphs could provide a better grasp of the decision-making of Graph Neural Networks. For that purpose, we introduce XP-GNN, a novel explanation technique for Graph Neural Networks in Knowledge Graphs. XP-GNN exploits the communities of nodes or edges in graphs to refine their explanations, inspired by cooperative game theory. We characterize XP-GNN in a basic example and in terms of scalability and stability. In two relevant use cases for the drug discovery pipeline, XP-GNN provides more relevant explanations than previous techniques, being evaluated quantitatively and by domain experts. At the same time, XP-GNN presents limitations on scalability and stability, which we will address. ACM Reference FormatAndres Martinez Mora, Dimitris Polychronopoulos, Michael Ughetto, and Sebastian Nilsson. 2024. Community-aware explanations in knowledge graphs with XP-GNN. In Proceedings of ACM Conference (Conference17). ACM, New York, NY, USA, 21 pages. https://doi.org/10.1145/nnnnnnn.nnnnnnn This work has been funded by AstraZeneca AB, Molndal, Sweden and AstraZeneca Cambridge. Unfortunately, due to proprietary reasons from AstraZeneca AB, the data used in this work cannot be shared.

bioinformatics↗

Biological Insights Knowledge Graph: an integrated knowledge graph to support drug development

The use of knowledge graphs as a data source for machine learning methods to solve complex problems in life sciences has rapidly become popular in recent years. Our Biological Insights Knowledge Graph (BIKG) combines relevant data for drug development from public as well as internal data sources to provide insights for a range of tasks: from identifying new targets to repurposing existing drugs. Besides the common requirements to organisational knowledge graphs such as being able to capture the domain precisely and give the users the ability to search and query the data, the focus on handling multiple use cases and supporting use case-specific machine learning models presents additional challenges: the data models must also be streamlined for the performance of downstream tasks; graph content must be easily customisable for different use cases; different projections of the graph content are required to support a wider range of different consumption modes. In this paper we describe our main design choices in implementation of the BIKG graph and discuss different aspects of its life cycle: from graph construction to exploitation.

systems biology↗

3D-Cardiomics: A spatial transcriptional atlas of the mammalian heart

Understanding spatial gene expression and regulation is key to uncovering developmental and physiological processes, during homeostasis and disease. Numerous techniques exist to gain gene expression and regulation information, but very few utilise intuitive true-to-life three-dimensional representations to analyze and visualize results. Here we combined spatial transcriptomics with 3D modelling to represent and interrogate, transcriptome-wide, three-dimensional gene expression and location in the mouse adult heart. Our study has unveiled specific subsets of genes that display complex spatial expression in organ sub-compartments. Also, we created a web-based user interface for spatial transcriptome analysis and visualization. The application may be accessed from http://3d-cardiomics.erc.monash.edu/.

systems biology↗