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Ho-Joon Lee

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Dr. Lee’s research in data science concerns biological questions in systems biology and network medicine by developing algorithms and models through a combination of statistical/machine learning, information theory, and network theory applied to multi-dimensional large-scale data. His projects have covered genomics, transcriptomics, proteomics, and metabolomics from yeast to mouse to human for integrative analysis of regulatory networks on multiple molecular levels, which also incorporates large-scale public databases such as GO for functional annotation, PDB for molecular structures, and PubChem and LINCS for drugs or small compounds. He previously carried out proteomics and metabolomics along with a computational derivation of dynamic protein complexes for IL-3 activation and cell cycle in murine pro-B cells (Lee et al., Cell Reports 2017), for which he developed integrative analytical tools using diverse approaches from machine learning and network theory. His ongoing interests in methodology include machine/deep learning and topological Kolmogorov-Sinai entropy-based network theory, which are applied to (1) multi-level dynamic regulatory networks in immune response, cell cycle, and cancer metabolism and (2) mass spectrometry-based omics data analysis.

Figure 1. Proteomics and metabolomics analysis of IL-3 activation and cell cycle (Lee et al., Cell Reports 2017). (A) Multi-omics abundance profiles of proteins, modules/complexes, intracellular metabolites, and extracellular metabolites over one cell cycle (from left to right columns) in response to IL-3 activation. Red for proteins/modules/intracellular metabolites up-regulation or extracellular metabolites release; Green for proteins/modules/intracellular metabolites down-regulation or extracellular metabolites uptake. (B) Functional module network identified from integrative analysis. Red nodes are proteins and white nodes are functional modules. Expression profile plots are shown for literature-validated functional modules. (C) Overall pathway map of IL-3 activation and cell cycle phenotypes. (D) IL-3 activation and cell cycle as a cancer model along with candidate protein and metabolite biomarkers. (E) Protein co-expression scale-free network. (F) Power-low degree distribution of the network E. (G) Protein entropy distribution by topological Kolmogorov-Sinai entropy calculated for the network E.

 

Jinseok Kim

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Jinseok Kim, Ph.D., is Research Assistant Professor in the Institute for Social Research at the University of Michigan, Ann Arbor.  Prof. Kim works on resolving named entity ambiguity in large-scale scholarly data (publication, patent, and funding records) in digital libraries. Especially, his current research is focused on developing methods for disambiguating author and affiliation names at a digital library scale using various supervised machine learning approaches trained on automatically labeled data . Disambiguated data from multiple sources will be integrated to be analyzed for insights into research production, scientific collaboration, funding evaluation, and research policy at a national level.

Peter Adriaens

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My research focus is on the development and application of machine learning tools to large scale financial and unstructured (textual) data to extract, quantify and predict risk profiles and investment grade rating of private and public companies.  Example datasets include social media and financial aggregators such as Bloomberg, Pitchbook, and Privco.

Z. Morley Mao

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Z. Morley Mao, PhD, is Professor of Electrical Engineering and Computer Science, College of Engineering, at the University of Michigan, Ann Arbor campus.

Sriram Chandrasekaran

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Sriram Chandrasekaran, PhD, is Assistant Professor of Biomedical Engineering in the College of Engineering at the University of Michigan, Ann Arbor.

Dr. Chandrasekaran’s Systems Biology lab develops computer models of biological processes to understand them holistically. Sriram is interested in deciphering how thousands of proteins work together at the microscopic level to orchestrate complex processes like embryonic development or cognition, and how this complex network breaks down in diseases like cancer. Systems biology software and algorithms developed by his lab are highlighted below and are available at http://www.sriramlab.org/software/.

– INDIGO (INferring Drug Interactions using chemoGenomics and Orthology) algorithm predicts how antibiotics prescribed in combinations will inhibit bacterial growth. INDIGO leverages genomics and drug-interaction data in the model organism – E. coli, to facilitate the discovery of effective combination therapies in less-studied pathogens, such as M. tuberculosis. (Ref: Chandrasekaran et al. Molecular Systems Biology 2016)

– GEMINI (Gene Expression and Metabolism Integrated for Network Inference) is a network curation tool. It allows rapid assessment of regulatory interactions predicted by high-throughput approaches by integrating them with a metabolic network (Ref: Chandrasekaran and Price, PloS Computational Biology 2013)

– ASTRIX (Analyzing Subsets of Transcriptional Regulators Influencing eXpression) uses gene expression data to identify regulatory interactions between transcription factors and their target genes. (Ref: Chandrasekaran et al. PNAS 2011)

– PROM (Probabilistic Regulation of Metabolism) enables the quantitative integration of regulatory and metabolic networks to build genome-scale integrated metabolic–regulatory models (Ref: Chandrasekaran and Price, PNAS 2010)

 

Research Overview: We develop computational algorithms that integrate omics measurements to create detailed genome-scale models of cellular networks. Some clinical applications of our algorithms include finding metabolic vulnerabilities in pathogens (M. tuberculosis) using PROM, and designing multi combination therapeutics for reducing antibiotic resistance using INDIGO.

Research Overview: We develop computational algorithms that integrate omics measurements to create detailed genome-scale models of cellular networks. Some clinical applications of our algorithms include finding metabolic vulnerabilities in pathogens (M. tuberculosis) using PROM, and designing multi combination therapeutics for reducing antibiotic resistance using INDIGO.

Jon Zelner

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Jon Zelner, PhD, is Assistant Professor in the department of Epidemiology in the University of Michigan School of Public Health. Dr. Zelner holds a second appointment in the Center for Social Epidemiology and Population Health.

Dr. Zelner’s research is focused on using spatial analysis, social network analyisis and dynamic modeling to prevent infectious diseases, with a focus on tuberculosis and diarrheal disease. Jon is also interested in understanding how the social and biological causes of illness interact to generate observable patterns of disease in space and in social networks, across outcomes ranging from infection to mental illness.

 

A large spatial cluster of multi-drug resistant tuberculosis (MDR-TB) cases in Lima, Peru is highlighted in red. A key challenge in my work is understanding why these cases cluster in space: can social, spatial, and genetic data tell us where transmission is occurring and how to interrupt it?

A large spatial cluster of multi-drug resistant tuberculosis (MDR-TB) cases in Lima, Peru is highlighted in red. A key challenge in my work is understanding why these cases cluster in space: can social, spatial, and genetic data tell us where transmission is occurring and how to interrupt it?

 

 

Adriene Beltz

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The goal of my research is to leverage network analysis techniques to uncover how the brain mediates sex hormone influences on gendered behavior across the lifespan. Specifically, my data science research concerns the creation and application of person-specific connectivity analyses, such as unified structural equation models, to time series data; these are intensive longitudinal data, including functional neuroimages, daily diaries, and observations. I then use these data science methods to investigate the links between androgens (e.g., testosterone) and estradiol at key developmental periods, such as puberty, and behaviors that typically show sex differences, including aspects of cognition and psychopathology.

A network map showing the directed connections among 25 brain regions of interest in the resting state frontoparietal network for an individual; data were acquired via functional magnetic resonance imaging. Black lines depict connections common across individuals in the sample, gray lines depict connections specific to this individual, solid lines depict contemporaneous connections (occurring in the same volume), and dashed lines depict lagged connections (occurring between volumes).

A network map showing the directed connections among 25 brain regions of interest in the resting state frontoparietal network for an individual; data were acquired via functional magnetic resonance imaging. Black lines depict connections common across individuals in the sample, gray lines depict connections specific to this individual, solid lines depict contemporaneous connections (occurring in the same volume), and dashed lines depict lagged connections (occurring between volumes).

Suleyman Uludag

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My research spans security, privacy, and optimization of data collection particularly as applied to the Smart Grid, an augmented and enhanced paradigm for the conventional power grid. I am particularly interested in optimization approaches that take a notion of security and/or privacy into the modeling explicitly. At the intersection of the Intelligent Transportation Systems, Smart Grid, and Smart Cities, I am interested in data privacy and energy usage in smart parking lots. Protection of data and availability, especially under assault through a Denial-of-Service attacks, represents another dimension of my area of research interests. I am working on developing data privacy-aware bidding applications for the Smart Grid Demand Response systems without relying on trusted third parties. Finally, I am interested in educational and pedagogical research about teaching computer science, Smart Grid, cyber security, and data privacy.

This figure shows the data collection model I used in developing a practical and secure Machine-to-Machine data collection protocol for the Smart Grid.

This figure shows the data collection model I used in developing a practical and secure
Machine-to-Machine data collection protocol for the Smart Grid.

Necmiye Ozay

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Necmiye Ozay, PhD, is Assistant Professor of Electrical Engineering and Computer Science, College of Engineering, at the University of Michigan, Ann Arbor.

Prof. Ozay and her team develop the scientific foundations and associated algorithmic tools for compactly representing and analyzing heterogeneous data streams from sensor/information-rich networked dynamical systems. They take a unified dynamics-based and data-driven approach for the design of passive and active monitors for anomaly detection in such systems. Dynamical models naturally capture temporal (i.e., causal) relations within data streams. Moreover, one can use hybrid and networked dynamical models to capture, respectively, logical relations and interactions between different data sources. They study structural properties of networks and dynamics to understand fundamental limitations of anomaly detection from data. By recasting information extraction problem as a networked hybrid system identification problem, they bring to bear tools from computer science, system and control theory and convex optimization to efficiently and rigorously analyze and organize information. The applications include diagnostics, anomaly and change detection in critical infrastructure such as building management systems, transportation and energy networks.

Ming Xu

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My research focuses on developing and applying computational and data-enabled methodology in the broader area of sustainability. Main thrusts are as follows:

  1. Human mobility dynamics. I am interested in mining large-scale real-world travel trajectory data to understand human mobility dynamics. This involves the processing and analyzing travel trajectory data, characterizing individual mobility patterns, and evaluating environmental impacts of transportation systems/technologies (e.g., electric vehicles, ride-sharing) based on individual mobility dynamics.
  2. Global supply chains. Increasingly intensified international trade has created a connected global supply chain network. I am interested in understanding the structure of the global supply chain network and economic/environmental performance of nations.
  3. Networked infrastructure systems. Many infrastructure systems (e.g., power grid, water supply infrastructure) are networked systems. I am interested in understanding the basic structural features of these systems and how they relate to the system-level properties (e.g., stability, resilience, sustainability).

A network visualization (force-directed graph) of the 2012 US economy using the industry-by-industry Input-Output Table (15 sectors) provided by BEA. Each node represents a sector. The size of the node represents the economic output of the sector. The size and darkness of links represent the value of exchanges of goods/services between sectors. An interactive version and other data visualizations are available at http://mingxugroup.org/