Elle O’Brien

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My research focuses on building infrastructure for public health and health science research organizations to take advantage of cloud computing, strong software engineering practices, and MLOps (machine learning operations). By equipping biomedical research groups with tools that facilitate automation, better documentation, and portable code, we can improve the reproducibility and rigor of science while scaling up the kind of data collection and analysis possible.

Research topics include:
1. Open source software and cloud infrastructure for research,
2. Software development practices and conventions that work for academic units, like labs or research centers, and
3. The organizational factors that encourage best practices in reproducibility, data management, and transparency

The practice of science is a tug of war between competing incentives: the drive to do a lot fast, and the need to generate reproducible work. As data grows in size, code increases in complexity and the number of collaborators and institutions involved goes up, it becomes harder to preserve all the “artifacts” needed to understand and recreate your own work. Technical AND cultural solutions will be needed to keep data-centric research rigorous, shareable, and transparent to the broader scientific community.

 

Ken Kollman

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I have been involved in the building of data infrastructure in the study of elections, political systems, violence, geospatial units, demographics, and topography. This infrastructure will eventually lead to the integration of data across many domains in the social, health, population, and behavioral sciences. My core research interests are in elections and political organizations.

Rajiv Saran

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Dr. Saran is an internationally recognized expert in kidney disease research – specifically, in the area of kidney disease surveillance and epidemiology. From 2014 – 2019, he served as Director of the United States Renal Data System (USRDS; www.usrds.org), a ‘gold standard’ for kidney disease data systems, worldwide. Since 2006 he has been Co-Principal Investigator for the Centers for the Disease Control and Prevention’s (CDC’s) National CKD Surveillance System for the US, a one of a kind project that complements the USRDS, while focusing on upstream surveillance of CKD and its risk factors (www.cdc.org/ckd/surveillance). Both projects have influenced policy related to kidney disease in the US and were cited extensively in the July 2019 Advancing American Kidney Health Federal policy document. Dr. Saran led the development of the first National Kidney Disease Information System (VA-REINS), for the Department of Veterans Affairs (VA), funded by the VA’s Center for Innovation, and one that led to the VA recognizing the importance of kidney disease as a health priority for US veterans. Dr. Saran has recently (2018-2021) been funded on a spin off project from VA REINS for investigation of ‘hot-spot’ of kidney disease among US Veterans involving both risk-prediction and geospatial analyses – a modern approach to health system big data being used for prevention and population health improvement, using kidney disease as an example. This approach has broad application for prevention and optimizing management of major chronic diseases.

Nambi Nallasamy

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Our team develops machine learning algorithms for the enhancement of outcomes in cataract surgery, the most commonly performed surgery in the world. Our works focuses on developing models for postoperative refraction after cataract surgery and analysis of surgical quality.

Donald S. Likosky

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Dr. Likosky is a Professor, Head of the Section of Health Services Research and Quality in the Department of Cardiac Surgery at Michigan Medicine and faculty member at the Center for Healthcare Outcomes and Policy. Dr. Likosky’s work currently focuses on leveraging: (i) mobile health technology to identify objective and scalable measures for mitigating post-surgical morbidities, and (ii) computer vision to identify objective and scalable measures of important intraoperative technical skills and non-technical practices.

Joshua Stein

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As a board-certified ophthalmologist and glaucoma specialist, I have more than 15 years of clinical experience caring for patients with different types and complexities of glaucoma. In addition to my clinical experience, as a health services researcher, I have developed experience and expertise in several disciplines including performing analyses using large health care claims databases to study utilization and outcomes of patients with ocular diseases, racial and other disparities in eye care, associations between systemic conditions or medication use and ocular diseases. I have learned the nuances of various data sources and ways to maximize our use of these data sources to answer important and timely questions. Leveraging my background in HSR with new skills in bioinformatics and precision medicine, over the past 2-3 years I have been developing and growing the Sight Outcomes Research Collaborative (SOURCE) repository, a powerful tool that researchers can tap into to study patients with ocular diseases. My team and I have spent countless hours devising ways of extracting electronic health record data from Clarity, cleaning and de-identifying the data, and making it linkable to ocular diagnostic test data (OCT, HVF, biometry) and non-clinical data. Now that we have successfully developed such a resource here at Kellogg, I am now collaborating with colleagues at > 2 dozen academic ophthalmology departments across the country to assist them with extracting their data in the same format and sending it to Kellogg so that we can pool the data and make it accessible to researchers at all of the participating centers for research and quality improvement studies. I am also actively exploring ways to integrate data from SOURCE into deep learning and artificial intelligence algorithms, making use of SOURCE data for genotype-phenotype association studies and development of polygenic risk scores for common ocular diseases, capturing patient-reported outcome data for the majority of eye care recipients, enhancing visualization of the data on easy-to-access dashboards to aid in quality improvement initiatives, and making use of the data to enhance quality of care, safety, efficiency of care delivery, and to improve clinical operations. .

Sunghee Lee

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My research focuses on issues in data collection with hard-to-reach populations. In particular, she examines 1) nontraditional sampling approaches for minority or stigmatized populations and their statistical properties and 2) measurement error and comparability issues for racial, ethnic and linguistic minorities, which also have implications for cross-cultural research/survey methodology. Most recently, my research has been dedicated to respondent driven sampling that uses existing social networks to recruit participants in both face-to-face and Web data collection settings. I plan to expand my research scope in examining representation issues focusing on the racial/ethnic minority groups in the U.S. in the era of big data.

Niccolò Meneghetti

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Dr. Niccolò Meneghetti is an Assistant Professor of Computer and Information Science at the University of Michigan-Dearborn.
His major research interests are in the broad area of database systems, with primary focus on probabilistic databases, statistical relational learning and uncertain data management.

Hernán López-Fernández

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I am interested in the evolutionary processes that originate “mega-diverse” biotic assemblages and the role of ecology in shaping the evolution of diversity. My program studies the evolution of Neotropical freshwater fishes, the most diverse freshwater fish fauna on earth, with an estimate exceeding 7,000 species. My lab combines molecular phylogenetics and phylogeny-based comparative methods to integrate ecology, functional morphology, life histories and geography into analyses of macroevolutionary patterns of freshwater fish diversification. We are also comparing patterns of diversification across major Neotropical fish clades. Relying on fieldwork and natural history collections, we use methods that span

Andrea Thomer

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Andrea Thomer is an assistant professor of information at the University of Michigan School of Information. She conducts research in the areas of data curation, museum informatics, earth science and biodiversity informatics, information organization, and computer supported cooperative work. She is especially interested in how people use and create data and metadata; the impact of information organization on information use; issues of data provenance, reproducibility, and integration; and long-term data curation and infrastructure sustainability. She is studying a number of these issues through the “Migrating Research Data Collections” project – a recently awarded Laura Bush 21st Century Librarianship Early Career Research Grant from the Institute of Museum and Library Services. Dr. Thomer received her doctorate in Library and Information Science from the School of Information Sciences at the University of Illinois at Urbana‐Champaign in 2017.