Imani Awarded $590K NIH Trailblazer Grant
ECE Assistant Professor Mahdi Imani was awarded a $590K NIH Trailblazer R21 grant for New and Early Stage Investigators from the National Institute of Biomedical Imaging and Bioengineering (NIBIB) for “Bayesian Dynamical Modeling of Microbial Communities”. This project seeks to develop efficient, interpretable, and scalable mathematical models and related tools for modeling and integrating various omics data, reconstructing the topology of microbial communities, and acquiring informative data.
Abstract Source: NIH
Microbial communities and their hosts play a key role in many applications, including protecting humans or plants against diseases or developing the next generation of biofuels and biological remediation systems needed for sustainable growth. Gaining a deep understanding of the fundamental biology of these systems is the key to har- nessing their potential. Advances in high-throughput multi-omics techniques like metagenomics, metatranscrip- tomics, exometabolomics, and proteomics, allow us to capture multiple snapshots of these complex biological processes at once. These snapshots create large-scale high-dimensional datasets of omics features (e.g., mi- crobial species, microbial genes, proteins, and small molecules). The reduced cost has also allowed researchers to collect more multi-omics time-series data. These temporally resolved multi-omics features can together provide a comprehensive picture of biological processes and their underlying activities. These well-designed multi-omics studies have not been analyzed to their fullest potential yet, primarily due to the lack of appropriate tools and annotation databases required for such analyses. For example, systematically investigating the time component of this longitudinal data to investigate the temporal dynamics of omics features in relationship with disease activities is an unmet need in many studies. Therefore, there is a critical need for statistical tools to greatly improve research infrastructure by integrating different data types and systematically investigating the time component of this longitudinal data. This project’s overarching goal is to develop efﬁcient, interpretable, and scalable tools based on our previously developed signal model, called partially-observed Boolean dynamical systems (POBDS), to characterize the time component and capture the dynamical behavior of microbial communities through multi-omics data. The original contributions can be organized across the following research goals: (i) Developing novel methods in the POBDS context capable of modeling multi-omics data obtained through various molecular proﬁling technologies and various diseases/domains. (ii) Developing Bayesian optimization frameworks for the efﬁcient and scalable reconstruction of the network topology of microbial communities (i.e., inferring the type of interactions between a large number of genes, bacteria, and microbes) through high dimensional multi-omics data. (iii) Developing Bayesian reinforcement learning perturbation policies to decrease the number of data required for the modeling/learning process (overcoming the non-identiﬁability issue) and acquire the most informative data in microbial communities. All the developed tools in this project will be presented in a user-friendly software/tool freely accessible to other researchers.