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Arkaprava Roy

dblp:281/9828 · DBLP profile ↗
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2ranked-venue papers
1as first author
2since 2021 · last 2024
—ORCID · conflict

Domains — the database's venue-derived domains; a paper can count in several

Artificial intelligence and machine learning · 1 · 1 first-author · 1 since 2021Applied, interdisciplinary, general and emerging computing · 1 · 1 since 2021

Expertise — from the expertise taxonomy: the topics of the expert's papers under the CCF categories. A weight counts papers with recency: 1 for a paper about the topic, 0.3 when the topic is its context, halved every five years.

Artificial intelligence
1 paper
Probabilistic and Bayesian machine learning · 50% Time series and sequential data · 50%

Topics — the 2 heaviest of 2, each with the papers that count most for it

TopicWeightPapersLastEvidence papers
Machine learning › Probabilistic and Bayesian machine learning › structured models › latent variable model
factor analysis
0.512021
Bayesian time-aligned factor analysis of paired multivariate time series · J. Mach. Learn. Res. 2021
Machine learning › Time series and sequential data
time series analysis
0.512021
Bayesian time-aligned factor analysis of paired multivariate time series · J. Mach. Learn. Res. 2021

Methods — techniques the papers use, named apart from their topics

warping functions · 0.5hamiltonian monte carlo · 0.5
YearPublicationVenuePosition
2024 Non parametric differential network analysis: a tool for unveiling specific molecular signatures
abstract
BACKGROUND: The rewiring of molecular interactions in various conditions leads to distinct phenotypic outcomes. Differential network analysis (DINA) is dedicated to exploring these rewirings within gene and protein networks. Leveraging statistical learning and graph theory, DINA algorithms scrutinize alterations in interaction patterns derived from experimental data. RESULTS: Introducing a novel approach to differential network analysis, we incorporate differential gene expression based on sex and gender attributes. We hypothesize that gene expression can be accurately represented through non-Gaussian processes. Our methodology involves quantifying changes in non-parametric correlations among gene pairs and expression levels of individual genes. CONCLUSIONS: Applying our method to public expression datasets concerning diabetes mellitus and atherosclerosis in liver tissue, we identify gender-specific differential networks. Results underscore the biological relevance of our approach in uncovering meaningful molecular distinctions.
Pietro H. Guzzi, Arkaprava Roy, Marianna Milano, Pierangelo Veltri
BMC Bioinform.2
2021 Bayesian time-aligned factor analysis of paired multivariate time series
abstract
Many modern data sets require inference methods that can estimate the shared and individual-specific components of variability in collections of matrices that change over time. Promising methods have been developed to analyze these types of data in static cases, but only a few approaches are available for dynamic settings. To address this gap, we consider novel models and inference methods for pairs of matrices in which the columns correspond to multivariate observations at different time points. In order to characterize common and individual features, we propose a Bayesian dynamic factor modeling framework called Time Aligned Common and Individual Factor Analysis (TACIFA) that includes uncertainty in time alignment through an unknown warping function. We provide theoretical support for the proposed model, showing identifiability and posterior concentration. The structure enables efficient computation through a Hamiltonian Monte Carlo (HMC) algorithm. We show excellent performance in simulations, and illustrate the method through application to a social mimicry experiment.
Arkaprava Roy, Jana Schaich Borg, David B. Dunson
J. Mach. Learn. Res.1