VLDB 2026 Research / reviewers in the wild / expert
Lucy Wang
dblp:144/5464
· DBLP profile ↗
5ranked-venue papers
1as first author
2since 2021 · last 2025
—ORCID · none
Domains — the database's venue-derived domains; a paper can count in several
Human-computer interaction and ubiquitous computing · 2 · 1 first-author · 1 since 2021Applied, interdisciplinary, general and emerging computing · 2Graphics, computer vision, multimedia, augmented reality and games · 1 · 1 first-author · 1 since 2021Theory of computation · 1 · 1 since 2021
| Year | Publication | Venue | Position |
|---|---|---|---|
| 2025 | Software for the Thompson and Funk Polygonal Geometry (Media Exposition)abstractMetric spaces defined within convex polygons, such as the Thompson, Funk, reverse Funk, and Hilbert metrics, are subjects of recent exploration and study in computational geometry. This paper contributes an educational piece of software for understanding these unique geometries while also providing a tool to support their research. We provide dynamic software for manipulating the Funk, reverse Funk, and Thompson balls in convex polygonal domains. Additionally, we provide a visualization program for traversing the Hilbert polygonal geometry. Hridhaan Banerjee, Carmen Isabel Day, Auguste H. Gezalyan, Olga Golovatskaia, Megan Hunleth, Sarah Hwang, Nithin Parepally, Lucy Wang, David M. Mount |
SoCG | 8 |
| 2021 | The Relationship between Personality, Game Motive, and Game Genre Preference: Gender as a ModeratorabstractThis study examined the relationships between players' Big Five personality traits, game motives, gender, and their game genre preference. Results revealed various associations between a player's personality traits and game motives as well as between personality, game motives and game genre preference. A player's gender was found to moderate the relationship between neuroticism personality trait and both escape motive and fantasy motive. Lucy Wang |
CoG | 1 |
| 2016 | SMART precision cancer medicine: a FHIR-based app to provide genomic information at the point of careabstractBACKGROUND: Precision cancer medicine (PCM) will require ready access to genomic data within the clinical workflow and tools to assist clinical interpretation and enable decisions. Since most electronic health record (EHR) systems do not yet provide such functionality, we developed an EHR-agnostic, clinico-genomic mobile app to demonstrate several features that will be needed for point-of-care conversations. METHODS: Our prototype, called Substitutable Medical Applications and Reusable Technology (SMART)® PCM, visualizes genomic information in real time, comparing a patient's diagnosis-specific somatic gene mutations detected by PCR-based hotspot testing to a population-level set of comparable data. The initial prototype works for patient specimens with 0 or 1 detected mutation. Genomics extensions were created for the Health Level Seven® Fast Healthcare Interoperability Resources (FHIR)® standard; otherwise, the prototype is a normal SMART on FHIR app. RESULTS: The PCM prototype can rapidly present a visualization that compares a patient's somatic genomic alterations against a distribution built from more than 3000 patients, along with context-specific links to external knowledge bases. Initial evaluation by oncologists provided important feedback about the prototype's strengths and weaknesses. We added several requested enhancements and successfully demonstrated the app at the inaugural American Society of Clinical Oncology Interoperability Demonstration; we have also begun to expand visualization capabilities to include cancer specimens with multiple mutations. DISCUSSION: PCM is open-source software for clinicians to present the individual patient within the population-level spectrum of cancer somatic mutations. The app can be implemented on any SMART on FHIR-enabled EHRs, and future versions of PCM should be able to evolve in parallel with external knowledge bases. Jeremy L. Warner, Matthew J. Rioth, Kenneth D. Mandl, Joshua C. Mandel, David A. Kreda, Isaac S. Kohane, Daniel Carbone, Ross Oreto, Lucy Wang, Shilin Zhu, Heming Yao, Gil Alterovitz |
J. Am. Medical Informatics Assoc. | 9 |
| 2016 | CUSTOM-SEQ: a prototype for oncology rapid learning in a comprehensive EHR environmentabstractBACKGROUND: As targeted cancer therapies and molecular profiling become widespread, the era of "precision oncology" is at hand. However, cancer genomes are complex, making mutation-specific outcomes difficult to track. We created a proof-of-principle, CUSTOM-SEQ: Continuously Updating System for Tracking Outcome by Mutation, to Support Evidence-based Querying, to automatically calculate and display mutation-specific survival statistics from electronic health record data. METHODS: Patients with cancer genotyping were included, and clinical data was extracted through a variety of algorithms. Results were refreshed regularly and injected into a standard reporting platform. Significant results were highlighted for visual cueing. A subset was additionally stratified by stage, smoking status, and treatment exposure. RESULTS: By August 2015, 4310 patients with a median follow-up of 17 months had sufficient data for survival calculation. As expected, epidermal growth factor receptor (EGFR) mutations in lung cancer were associated with superior overall survival, hazard ratio (HR) = 0.53 (P < .001), validating the approach. Guanine nucleotide binding protein (G protein), q polypeptide (GNAQ) mutations in melanoma were associated with inferior overall survival, a novel finding (HR = 3.42, P < .001). Smoking status was not prognostic for epidermal growth factor receptor-mutated lung cancer patients, who also lived significantly longer than their counterparts, even with advanced disease (HR = 0.54, P = .001). INTERPRETATION: CUSTOM-SEQ represents a novel rapid learning system for a precision oncology environment. Retrospective studies are often limited by study of specific time periods and can lead to incomplete conclusions. Because data is continuously updated in CUSTOM-SEQ, the evidence base is constantly growing. Future work will allow users to interactively explore populations by demographics and treatment exposure, in order to further investigate significant mutation-specific signals. Jeremy L. Warner, Lucy Wang, William Pao, Jeffrey A. Sosman, Ravi V. Atreya, Pam Carney, Mia A. Levy |
J. Am. Medical Informatics Assoc. | 2 |
| 2014 | Emergent, crowd-scale programming practice in the IDEabstractWhile emergent behaviors are uncodified across many domains such as programming and writing, interfaces need explicit rules to support users. We hypothesize that by codifying emergent programming behavior, software engineering interfaces can support a far broader set of developer needs. To explore this idea, we built Codex, a knowledge base that records common practice for the Ruby programming language by indexing over three million lines of popular code. Codex enables new data-driven interfaces for programming systems: statistical linting, identifying code that is unlikely to occur in practice and may constitute a bug; pattern annotation, automatically discovering common programming idioms and annotating them with metadata using expert crowdsourcing; and library generation, constructing a utility package that encapsulates and reflects emergent software practice. We evaluate these applications to find Codex captures a broad swatch of programming practice, statistical linting detects problematic code snippets, and pattern annotation discovers nontrivial idioms such as basic HTTP authentication and database migration templates. Our work suggests that operationalizing practice-driven knowledge in structured domains such as programming can enable a new class of user interfaces. Ethan Fast, Daniel Steffee, Lucy Wang, Joel Brandt, Michael S. Bernstein |
CHI | 3 |