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Gennari, J.

Publications and source records attributed to Gennari, J..

4 recordsLinked to original sources

TabularQual: A spreadsheet-based format for annotating and curating logical models in SBML-qual

Logical models are widely used to study regulatory and signaling systems, yet their reuse, annotation, and exchange across tools remain challenging. Although SBML Level 3 Qualitative Models (SBML-qual) provides a standard representation, its XML-based syntax is difficult to inspect and edit directly. Here we introduce TabularQual, a spreadsheet-based, community-driven representation for Boolean and multi-valued logical models, together with a bidirectional converter between spreadsheets and SBML-qual. The converter is accessible programmatically and via a web interface to support diverse user workflows. We further describe two integration strategies that enable existing modeling tools to operate with TabularQual, either through SBML-qual exchange or via direct support. Case studies using the Stress Knowledge Map and CaSQ demonstrate how this integration supports model construction, curation, and reuse. TabularQual provides a practical bridge between human-readable model representations and standardized executable formats, supporting reproducibility, interoperability, and community-driven model development.

systems biology↗

KGBN: Augmenting and optimizing logical gene regulatory networks using knowledge graphs

Logical gene regulatory network (GRN) models provide interpretable, mechanistic representations of cellular regulation and are widely used in systems biology. However, most existing models remain incomplete, context-specific, and difficult to extend to comprehensive GRNs, limiting their broader applicability to tasks such as drug-response prediction and precision medicine. Here, add some ideas about virtual twins: With AML patients, we can use comprehensive GRNs to predict drug response. We present KGBN (Knowledge Graph-augmented Boolean Network modeling), a computational workflow for systematically augmenting logical GRN models. KGBN incorporates regulatory interactions derived from curated knowledge graphs as alternative logical rules while preserving the validated structure of existing models. Rule probabilities are optimized against experimental data to represent regulatory uncertainty and achieve data-driven calibration. Applying KGBN to acute myeloid leukemia, we show that extending an existing GRN with drug-target pathways and training against ex vivo drug-response data yields mutation-specific models that recapitulate known therapeutic sensitivities and signaling dependencies, demonstrating the utility of KGBN for interpretable, context-aware GRN modeling. (Should be predict)

systems biology↗

Using SED-ML for reproducible curation: Verifying BioModels across multiple simulation engines

The BioModels Repository contains over 1000 manually curated mechanistic models from published literature, most often encoded in the Systems Biology Markup Language (SBML). This community-based standard formally specifies each model, but does not describe the computational experimental conditions to run a simulation. Therefore, it can be challenging to reproduce any figure or result from a publication with an SBML model alone. The Simulation Experiment Description Markup Language (SED-ML) provides a solution: a standard way to specify exactly how to run an experiment corresponding to a specific figure or result. BioModels was established years before SED-ML, and both systems evolved over time, both in content and acceptance. Hence, only about half of the entries in BioModels contained SED-ML files, and these files reflected the version of SED-ML that was available at the time. Additionally, almost all of these SED-ML files had at least one minor mistake that made them invalid. To make these models and their results more reproducible, we report here on our work updating, correcting and generating new SED-ML files for 1055 curated mechanistic models in BioModels. In addition, because SED-ML is implementation-independent, it can be used for verification, demonstrating that results hold across multiple simulation engines. We tested, corrected, and improved over 450 existing SED-ML files in the BioModels database, and created basic files for the rest of the entries. Then, we used a wrapper architecture for interpreting SED-ML, and report verification results across five different ODE-based biosimulation engines, after further improving the models, the wrappers, and the engines themselves. Our work with SED-ML and the BioModels collection aims to improve the utility of these models by making them more reproducible and credible. Improved reproducibility means these models are now even more fit for re-use, such as in new investigations and as components of multiscale models. Author summaryReproducing computationally-derived scientific results seems like it should be straightforward, but is often elusive. Code is lost, file formats change, and knowledge of what was done is only partially recorded and/or forgotten. Model repositories such as BioModels address this failing in the Systems Biology domain by encoding models in a standard format that can reproduce a figure from the paper from which it was drawn. Here, we delved into the BioModels repository to create and correct the instructions on what to do with every curated model, and then tested those instructions on a variety of simulation platforms, allowing us to find and correct issues with the platforms and the simulators themselves. Not only did this improve the BioModels repository, but also improved the infrastructure necessary to run these verification comparisons in the future, and improved the fitness of the models for re-use by other researchers.

systems biology↗

Merging logical models: An application in Acute Myeloid Leukemia modeling

MotivationGene regulatory network (GRN) models provide mechanistic understanding of genetic interactions that regulate gene expression and, consequently, influence cellular behavior. Dysregulated gene expression plays a critical role in disease progression and treatment response, making GRN models a promising tool for precision medicine. While researchers have built many models to describe specific subsets of gene interactions, more comprehensive models that cover a broader range of genes are challenging to build. This necessitates the development of automated approaches for merging existing models. ResultsWe present LM-Merger, a workflow for semi-automatically merging logical GRN models. The workflow consists of five main steps: (a) model identification, (b) model standardization and annotation, (c) model verification, (d) model merging, and (d) model evaluation. We demonstrate the feasibility and benefit of this workflow with two pairs of published models pertaining to acute myeloid leukemia (AML). The integrated models were able to retain the predictive accuracy of the original models, while expanding coverage of the biological system. Notably, when applied to a new dataset, the integrated models outperformed the individual models in predicting patient response. This study highlights the potential of logical model merging to advance systems biology research and our understanding of complex diseases. Availability and implementationThe workflow and accompanying tools, including modules for model standardization, automated logical model merging, and evaluation, are available at https://github.com/IlyaLab/LogicModelMerger/.

systems biology↗