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  1. Evaluation of background prediction for variant detection in a clinical context : towards improved NGS monitoring of minimal residual disease in hematological malignancies

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  2. Transitions between electronic health record systems: experiences from diverse health systems

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  3. Building a large public database of de-identified electrocardiogram data from a single emergency department

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  4. Modeling and simulation of processes in GI endoscopy

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  5. Batch effect detection and network analysis in BCR/ABL-independent CML imatinib resistance

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  6. Team cognition in context: application of novel methods and metrics to characterize team performance in pediatric emergency medicine

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  7. The Impact of standardized pediatric opioid and antibiotic medications on medication adjustments and staff satisfaction

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  8. Social media as a medical survey research recruitment tool: examining patient experience with inferior vena cava filters

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  9. Implementation and evaluation of a semantic workflow for neuroimage processing

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  10. Effect of patient decision aids on changes in men's prostate cancer screening behavior: a systematic review and meta-analysis

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  11. Women's cancer screening decision aid for arabic speaking women

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  12. Development of a network-based measure of genetic risk and its application in preterm birth and retinopathy of prematurity

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  13. VarGraph: a decision support tool for variant classification using pathway databases

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  14. Design and Implementation Considerations for a Clinical Decision Support Knowledge Management Repository

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  15. Genomic Instability of Solid Tumors and Clinical Applications

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  16. Developing a Comprehensive Statewide Smoking Cessation Plan for IU Health: Leveraging a connection with the Indiana Tobacco Quitline

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  17. The Current State of mHealth Applications for the Treatment of Depression

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  18. Elucidating Molecular Mechanisms of HPV-Positive Head and Neck Squamous Cell Carcinoma

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  19. Internists' perceptions regarding patient access to progress notes

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  20. Comparative analysis of semantic similarity and gene orthology tools for identification of gene candidates for human diseases

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