Demo Data from EDBT 2026 / reviewers in the wild / expert
Mattia G. Gollub
dblp:221/4158
· DBLP profile ↗
2ranked-venue papers
2as first author
2since 2021 · last 2024
0000-0001-9588-3130ORCID · corroborated
Domains — the database's venue-derived domains; a paper can count in several
Applied, interdisciplinary, general and emerging computing · 2 · 2 first-author · 2 since 2021
Expertise — from the expertise taxonomy: the topics of the expert's papers under the CCF categories. A weight counts papers with recency: 1 for a paper about the topic, 0.3 when the topic is its context, halved every five years.
| Interdisciplinary, comprehensive, and emerging computing
2 papers |
Bioinformatics and computational biology · 100% |
Topics — the 5 heaviest of 5, each with the papers that count most for it
| Topic | Weight | Papers | Last | Evidence papers |
|---|---|---|---|---|
Bioinformatics and computational biology
systems biology |
1.3 | 2 | 2024 | ENKIE: a package for predicting enzyme kinetic parameter values and their uncertainties · Bioinform. 2024 Probabilistic thermodynamic analysis of metabolic networks · Bioinform. 2021 |
Bioinformatics and computational biology › systems biology
enzyme kinetics |
0.8 | 1 | 2024 | ENKIE: a package for predicting enzyme kinetic parameter values and their uncertainties · Bioinform. 2024 |
Bioinformatics and computational biology › systems biology
metabolic network analysis |
0.5 | 1 | 2021 | Probabilistic thermodynamic analysis of metabolic networks · Bioinform. 2021 |
Bioinformatics and computational biology › systems biology › constraint-based modeling
thermodynamics-based flux analysis |
0.5 | 1 | 2021 | Probabilistic thermodynamic analysis of metabolic networks · Bioinform. 2021 |
Bioinformatics and computational biology › systems biology
metabolic modeling |
0.2 | 1 | 2024 | ENKIE: a package for predicting enzyme kinetic parameter values and their uncertainties · Bioinform. 2024 |
Methods — techniques the papers use, named apart from their topics
bayesian multilevel model · 0.8thermodynamic constraints · 0.5probabilistic optimization · 0.5joint sampling · 0.5
| Year | Publication | Venue | Position |
|---|---|---|---|
| 2024 | ENKIE: a package for predicting enzyme kinetic parameter values and their uncertaintiesabstractMOTIVATION: Relating metabolite and enzyme abundances to metabolic fluxes requires reaction kinetics, core elements of dynamic and enzyme cost models. However, kinetic parameters have been measured only for a fraction of all known enzymes, and the reliability of the available values is unknown. RESULTS: The ENzyme KInetics Estimator (ENKIE) uses Bayesian Multilevel Models to predict value and uncertainty of KM and kcat parameters. Our models use five categorical predictors and achieve prediction performances comparable to deep learning approaches that use sequence and structure information. They provide calibrated uncertainty predictions and interpretable insights into the main sources of uncertainty. We expect our tool to simplify the construction of priors for Bayesian kinetic models of metabolism. AVAILABILITY AND IMPLEMENTATION: Code and Python package are available at https://gitlab.com/csb.ethz/enkie and https://pypi.org/project/enkie/. Mattia G. Gollub, Thierry Backes, Hans-Michael Kaltenbach, Jörg Stelling |
Bioinform. | 1 |
| 2021 | Probabilistic thermodynamic analysis of metabolic networksabstractMOTIVATION: Random sampling of metabolic fluxes can provide a comprehensive description of the capabilities of a metabolic network. However, current sampling approaches do not model thermodynamics explicitly, leading to inaccurate predictions of an organism's potential or actual metabolic operations. RESULTS: We present a probabilistic framework combining thermodynamic quantities with steady-state flux constraints to analyze the properties of a metabolic network. It includes methods for probabilistic metabolic optimization and for joint sampling of thermodynamic and flux spaces. Applied to a model of Escherichia coli, we use the methods to reveal known and novel mechanisms of substrate channeling, and to accurately predict reaction directions and metabolite concentrations. Interestingly, predicted flux distributions are multimodal, leading to discrete hypotheses on E.coli's metabolic capabilities. AVAILABILITY AND IMPLEMENTATION: Python and MATLAB packages available at https://gitlab.com/csb.ethz/pta. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online. Mattia G. Gollub, Hans-Michael Kaltenbach, Jörg Stelling |
Bioinform. | 1 |