Enhancing Data Analysis & Reporting Capacity for Program Evaluation Abstract The objective of the Cellular and Molecular Biology Umbrella Training Program (T32 GM007067) in the Division of Biology and Biomedical Sciences (DBBS) at Washington University is to provide rigorous, interdisciplinary training in cell and molecular biology to a diverse cohort of students, enabling them to pursue careers at the vanguard of scientific research, education, and outreach. Its educational mission aims to ground students in the basic concepts and methodologies of cell and molecular biology, train them to think critically as well as write and speak effectively. In this effort, our guiding philosophy is to extend all successful program elements to as many students as possible in order to maximize the training of all our students and thus the future impact of our students on society. To support the training objectives and continuous program improvement of the parent T32 grant (T32 GM007067), DBBS aims to enhance capacity for data-driven program evaluation. DBBS collects comprehensive data at each stage of student training to track the progress of students in 12 DBBS interdisciplinary bioscience Ph.D. programs, including those supported by the parent T32 grant and other NIH-funded T32 grants at Washington University in St. Louis. To support data-driven program improvements, additional evaluation and assessment capacity is needed for data analysis and reporting. An administrative supplement from NIGMS will allow DBBS to 1) Mine our data to perform current-state baseline analysis of our programs, 2) Build technical and operational capacity for sustainable longitudinal program evaluation and continuous improvement, and 3) Disseminate our evaluation model and baseline data to the bioscience Ph.D. training community. These activities will synergize and enhance, but not duplicate, program data collection efforts currently underway. Since 2017, DBBS has been working on curriculum modernization, defined Core Competencies and subcompetencies that constitute the full scope of biomedical Ph.D. training in our programs, and will launch a new required Graduate Research Fundamentals course in fall 2020. This new course will enhance instruction in foundational scientific skills emphasized by NIGMS, including methods to enhance rigor and reproducibility, quantitative reasoning, scientific communication, and interpersonal skills such as professionalism and bias mitigation to enhance diversity, equity, and inclusion. With new curriculum launching in the fall, the time is right to perform a current-state baseline analysis of existing program evaluation data and to evaluate the effects of new training curriculum. The activities proposed will build the technical and operational capacity to evaluate the impacts of new Ph.D. training curriculum and enable data-driven decision-making for continuous curriculum improvement.

Public Health Relevance

Enhancing Data Analysis & Reporting Capacity for Program Evaluation Project Narrative The objective of the Cellular and Molecular Biology Umbrella Training Program (T32 GM007067) in the Division of Biology and Biomedical Sciences (DBBS) at Washington University is to provide rigorous, interdisciplinary training in cell and molecular biology to a diverse cohort of students, enabling them to pursue careers at the vanguard of scientific research, education, and outreach. To support data-driven program improvements, additional evaluation and assessment capacity is needed to 1) Mine our data to perform current-state baseline analysis of our programs, 2) Build technical and operational capacity for sustainable longitudinal program evaluation and continuous improvement, and 3) Disseminate our evaluation model and baseline data to the bioscience Ph.D. training community. The activities proposed will build the technical and operational capacity to evaluate the impacts of new Ph.D. training curriculum and enable data-driven decision-making for continuous curriculum improvement.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Institutional National Research Service Award (T32)
Project #
3T32GM007067-46S1
Application #
10154340
Study Section
Special Emphasis Panel (ZGM1)
Program Officer
Gindhart, Joseph G
Project Start
1975-07-01
Project End
2021-06-30
Budget Start
2020-07-01
Budget End
2021-06-30
Support Year
46
Fiscal Year
2020
Total Cost
Indirect Cost
Name
Washington University
Department
Anatomy/Cell Biology
Type
Schools of Medicine
DUNS #
068552207
City
Saint Louis
State
MO
Country
United States
Zip Code
63130
Potter, R F; Wallace, M A; McMullen, A R et al. (2018) blaIMP-27 on transferable plasmids in Proteus mirabilis and Providencia rettgeri. Clin Microbiol Infect 24:1019.e5-1019.e8
Potter, Robert F; Lainhart, William; Twentyman, Joy et al. (2018) Population Structure, Antibiotic Resistance, and Uropathogenicity of Klebsiella variicola. MBio 9:
Zhao, Yu; Mudge, Miranda C; Soll, Jennifer M et al. (2018) OTUD4 Is a Phospho-Activated K63 Deubiquitinase that Regulates MyD88-Dependent Signaling. Mol Cell 69:505-516.e5
Burclaff, Joseph; Mills, Jason C (2018) Plasticity of differentiated cells in wound repair and tumorigenesis, part II: skin and intestine. Dis Model Mech 11:
Berry, Kayla N; Kober, Daniel L; Su, Alvin et al. (2018) Limiting Respiratory Viral Infection by Targeting Antiviral and Immunological Functions of BST-2/Tetherin: Knowledge and Gaps. Bioessays 40:e1800086
Murali, Bhavna; Ren, Qihao; Luo, Xianmin et al. (2018) Inhibition of the Stromal p38MAPK/MK2 Pathway Limits Breast Cancer Metastases and Chemotherapy-Induced Bone Loss. Cancer Res 78:5618-5630
Cottrell, Kyle A; Chaudhari, Hemangi G; Cohen, Barak A et al. (2018) PTRE-seq reveals mechanism and interactions of RNA binding proteins and miRNAs. Nat Commun 9:301
Ferreiro, Aura; Crook, Nathan; Gasparrini, Andrew J et al. (2018) Multiscale Evolutionary Dynamics of Host-Associated Microbiomes. Cell 172:1216-1227
Brettmann, Erin A; Lye, Lon-Fye; Beverley, Stephen M (2018) Spontaneous excision and facilitated recovery as a control for phenotypes arising from RNA interference and other dominant transgenes. Mol Biochem Parasitol 220:42-45
Ohlemacher, Shannon I; Xu, Yiquan; Kober, Daniel L et al. (2018) YbtT is a low-specificity type II thioesterase that maintains production of the metallophore yersiniabactin in pathogenic enterobacteria. J Biol Chem 293:19572-19585

Showing the most recent 10 out of 267 publications