bioRxiv Science⌕ Search

Biology subjects

Malpani, T.

Publications and source records attributed to Malpani, T..

2 recordsLinked to original sources

FROG Analysis Ensures the Reproducibility of Genome Scale Metabolic Models

Genome-scale metabolic models (GEMs) and other constraint-based models (CBMs) play a pivotal role in understanding biological phenotypes and advancing research in areas like metabolic engineering, human disease modelling, drug discovery, and personalized medicine. Despite their growing application, a significant challenge remains in ensuring the reproducibility of GEMs, primarily due to inconsistent reporting and inadequate model documentation of model results. Addressing this gap, we introduce FROG analysis, a community-driven initiative aimed at standardizing reproducibility assessments of CBMs and GEMs. The FROG framework encompasses four key analyses--Flux variability, Reaction deletion, Objective function, and Gene deletion--to produce standardized, numerically reproducible FROG reports. These reports serve as reference datasets, enabling model evaluators, curators, and independent researchers to verify the reproducibility of GEMs systematically. BioModels, a leading repository of systems biology models, has integrated FROG analysis into its curation workflow, enhancing the reproducibility and reusability of submitted GEMs. In our study evaluating 65 GEM submissions from the community, approximately 40% reproduced without intervention, 28% requiring minor adjustments, and 32% needing input from authors. The standardization introduced by FROG analysis facilitated the detection and resolution of issues, ultimately leading to the successful reproduction of all models. By establishing a standardized and comprehensive approach to evaluating GEM reproducibility, FROG analysis significantly contributes to making CBMs and GEMs more transparent, reusable, and reliable for the broader scientific community.

systems biology↗

Understanding flux switching in metabolic networks through an analysis of synthetic lethals

Biological systems are extremely robust and exhibit high levels of redundancy for multiple cellular functions. Some of this redundancy manifests as alternative pathways in metabolism. Synthetic double lethals in metabolic networks comprise pairs of reactions, which, when deleted simultaneously, abrogate cell growth. However, when one reaction from such pairs is removed, the cell reroutes its metabolites through alternative pathways. Very little is known about the set of reactions through which fluxes are rerouted. Analysing this redistribution would help us to uncover the linkage between the reactions in a synthetic double lethal and also understand the complexity underlying the reroutings. Studying synthetic lethality in the context of pathogenic bacteria can offer valuable insights into therapeutic interventions. In this work, we propose a constraint-based approach to unravel these alternate pathways and complex interdependencies within and across metabolic modules. The approach involves a generic optimisation that minimises the extent of rerouting between two reaction deletions, corresponding to synthetic lethal pairs. We also include a systematic analysis of synthetic lethals by identifying the reaction classes that make up these synthetic lethals. We applied our computational workflow to several existing high-quality genome-scale models to show that these rerouted reactions span across metabolic modules, thereby illustrating the complexity and uniqueness of metabolism. Our results provide interesting insights into the organisation of metabolic networks and their redundancy. The algorithm is available at https://github.com/RamanLab/minRerouting. Contact: kraman@iitm.ac.in

systems biology↗