Devika Subramanian

Dr. Devika Subramanian


Research Focus & Metrics

Academic Career Length

22Years (2005-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 December 2011 in Journal of Infrastructure Systems
Verified
Journal Article
Closed access
JWJames Winkler
James Winkler
LDLeonardo Dueñas-Osorio
Leonardo Dueñas-Osorio
RSRobert M. Stein
Robert M. Stein
DSDevika Subramanian
Devika Subramanian
The reliability assessment of infrastructure systems providing power, natural gas, and potable water is an integral part of societal preparedness to unforeseen hazards. The topological properties of interface networks connecting electric substations to water pumping stations and natural gas compressors have received little attention, despite the key role these connections play in operation and failure propagation. This work introduces a performance assessment methodology for coupled infrastructures that links physical fragility modeling with the topology of realistic and ideal connecting interfaces. Distinct interfaces based on features such as betweenness, clustering, vertex degree, and Euclidean distance are assessed regarding their role in connecting utility systems and propagating failures from random and hurricane events in Harris County, Texas. The interface minimizing the Euclidean distance between electric substations and other utility nodes exhibits a slow performance decline as random failures i...

1 July 2011 in Circulation: Heart Failure
Verified
Journal Article
Closed access
PDF file
DSDevika Subramanian
Devika Subramanian
VSVenkataraman Subramanian
Venkataraman Subramanian
ADAnita Deswal
Anita Deswal
DMDouglas L Mann
Douglas L Mann
UJUpshaw J
Upshaw J
DKDavid M. Kent
David M. Kent
Morbidity and mortality rates associated with heart failure remain high. A wide variety of demographic and clinical factors as well as biomarkers are associated with increased mortality rates. Despite this, most multivariate predictive models for heart failure mortality have predictive accuracies characterized by a C-statistic (area under the receiver operating curve) of ≈0.74. We analyzed data on 963 patients enrolled in the Vesnarinone Evaluation of Survival Trial (VEST), including circulating levels of 2 cytokines (tumor necrosis factor and interleukin-6) and their receptors sampled at baseline and at 8, 16, and 24 weeks. We built multivariate logistic regression models by using standard clinical variables and time-series of cytokine and cytokine receptor levels, using independent components analysis to handle collinearity among cytokine measurements, and L2-penalized stepwise regression for variable selection. We also built ensemble models with these data, using gentle boosting. Our multivariate logistic regression model using time-series cytokine measurements predicts 1-year mortality rates significantly better ( P =0.001) than the baseline model, with a C-statistic of 0.81±0.03. Without the cytokines, the baseline model has a C-statistic of 0.73±0.03, and, with only baseline cytokine and cytokine receptor levels added, the model has a C-statistic of 0.74±0.04. An ensemble model of 100 decision stumps with serial cytokine measurements has a significantly better ( P =0.04) C-statistic of 0.84±0.02. An ensemble model with baseline cytokine data and without the serial measurements has a C-statistic of 0.74±0.04. Significant gains in accuracy of one year mortality prediction in chronic heart failure can be obtained by using logistic regression models that incorporate serial measurements of biomarkers such as cytokine and cytokine receptor levels. Ensemble models capture inherent variability in large patient populations, and boost predictive accuracy through the use of time-series measurements.

24 August 2012 in BMC Bioinformatics
Verified
Journal Article
Open access
PDF file
BBBradley M Broom
Bradley M Broom
KDKim-anh Do
Kim-anh Do
DSDevika Subramanian
Devika Subramanian
Considerable progress has been made on algorithms for learning the structure of Bayesian networks from data. Model averaging by using bootstrap replicates with feature selection by thresholding is a widely used solution for learning features with high confidence. Yet, in the context of limited data many questions remain unanswered. What scoring functions are most effective for model averaging? Does the bias arising from the discreteness of the bootstrap significantly affect learning performance? Is it better to pick the single best network or to average multiple networks learnt from each bootstrap resample? How should thresholds for learning statistically significant features be selected?

8 September 2023 in The Journal of Clinical Endocrinology & Metabolism
Verified
Journal Article
Open access
PDF file
NPNikita Pozdeyev
Nikita Pozdeyev
MDManjiri Kiran Dighe
Manjiri Kiran Dighe
MBMartin Barrio
Martin Barrio
CRChristopher Raeburn
Christopher Raeburn
HSHarry A Smith
Harry A Smith
TCTrevor Cohen
Trevor Cohen
Context: Thyroid nodule ultrasound-based risk stratification schemas rely on the presence of high-risk sonographic features. However, some malignant thyroid nodules have benign appearance on thyroid ultrasound. New methods for thyroid nodule risk assessment are needed. Objective: We investigated polygenic risk score (PRS) accounting for inherited thyroid cancer risk combined with ultrasound-based analysis for improved thyroid nodule risk assessment. Methods: The convolutional neural network classifier was trained on thyroid ultrasound still images and cine clips from 621 thyroid nodules. Phenome-wide association study (PheWAS) and PRS PheWAS were used to optimize PRS for distinguishing benign and malignant nodules. PRS was evaluated in 73 346 participants in the Colorado Center for Personalized Medicine Biobank. Results: When the deep learning model output was combined with thyroid cancer PRS and genetic ancestry estimates, the area under the receiver operating characteristic curve (AUROC) of the benign vs malignant thyroid nodule classifier increased from 0.83 to 0.89 (DeLong, P value = .007). The combined deep learning and genetic classifier achieved a clinically relevant sensitivity of 0.95, 95% CI [0.88-0.99], specificity of 0.63 [0.55-0.70], and positive and negative predictive values of 0.47 [0.41-0.58] and 0.97 [0.92-0.99], respectively. AUROC improvement was consistent in European ancestry-stratified analysis (0.83 and 0.87 for deep learning and deep learning combined with PRS classifiers, respectively). Elevated PRS was associated with a greater risk of thyroid cancer structural disease recurrence (ordinal logistic regression, P value = .002). Conclusion: Augmenting ultrasound-based risk assessment with PRS improves diagnostic accuracy.

15 June 2005 in ACM SIGPLAN Notices
Verified
Journal Article
Open access
KCKeith D. Cooper
Keith D. Cooper
AGAlexander Grosul
Alexander Grosul
THTimothy J. Harvey
Timothy J. Harvey
SRSteven Reeves
Steven Reeves
DSDevika Subramanian
Devika Subramanian
TWTodd Waterman
Todd Waterman
Research over the past five years has shown significant performance improvements using a technique called adaptive compilation . An adaptive compiler uses a compile-execute-analyze feedback loop to find the combination of optimizations and parameters that minimizes some performance goal, such as code size or execution time.Despite its ability to improve performance, adaptive compilation has not seen widespread use because of two obstacles: the large amounts of time that such systems have used to perform the many compilations and executions prohibits most users from adopting these systems, and the complexity inherent in a feedback-driven adaptive system has made it difficult to build and hard to use.A significant portion of the adaptive compilation process is devoted to multiple executions of the code being compiled. We have developed a technique called virtual execution to address this problem. Virtual execution runs the program a single time and preserves information that allows us to accurately predict the performance of different optimization sequences without running the code again. Our prototype implementation of this technique significantly reduces the time required by our adaptive compiler.In conjunction with this performance boost, we have developed a graphical-user interface (GUI) that provides a controlled view of the compilation process. By providing appropriate defaults, the interface limits the amount of information that the user must provide to get started. At the same time, it lets the experienced user exert fine-grained control over the parameters that control the system.

1 July 2021 in Journal of Biomedical Informatics
Verified
Journal Article
Closed access
XDXiruo Ding
Xiruo Ding
JMJustin Mower
Justin Mower
DSDevika Subramanian
Devika Subramanian
TCTrevor Cohen
Trevor Cohen