arXiv subjects

Methun Kamruzzaman

Publications and source records attributed to Methun Kamruzzaman.

5 recordsLinked to original sources

arXiv2025

Prediction of Hospital Associated Infections During Continuous Hospital Stays

The US Centers for Disease Control and Prevention (CDC), in 2019, designated Methicillin-resistant Staphylococcus aureus (MRSA) as a serious antimicrobial resistance threat. The risk of acquiring MRSA and suffering life-threatening consequences due to it remains especially high for hospitalized patients due to a unique combination of factors, including: co-morbid conditions, immuno suppression, antibiotic use, and risk of contact with contaminated hospital workers and equipment. In this paper, we present a novel generative probabilistic model, GenHAI, for modeling sequences of MRSA test results outcomes for patients during a single hospitalization. This model can be used to answer many important questions from the perspectives of hospital administrators for mitigating the risk of MRSA infections. Our model is based on the probabilistic programming paradigm, and can be used to approximately answer a variety of predictive, causal, and counterfactual questions. We demonstrate the efficacy of our model by comparing it against discriminative and generative machine learning models using two real-world datasets.

cs.LG↗

arXiv2025

Polarized and unpolarized gluon PDFs: generative machine learning applications for lattice QCD matrix elements at short distance and large momentum

Lattice quantum chromodynamics (QCD) calculations share a defining challenge by requiring a small finite range of spatial separation $z$ between quark/gluon bilinears for controllable power corrections in the perturbative QCD factorization, and a large hadron boost $p_z$ for a successful determination of collinear parton distribution functions (PDFs). However, these two requirements make the determination of PDFs from lattice data very challenging. We present the application of generative machine learning algorithms to estimate the polarized and unpolarized gluon correlation functions utilizing short-distance data and extending the correlation up to $zp_z \lesssim 14$, surpassing the current capabilities of lattice QCD calculations. We train physics-informed machine learning algorithms to learn from the short-distance correlation at $z\lesssim 0.36$ fm and take the limit, $p_z \to \infty$, thereby minimizing possible contamination from the higher-twist effects for a successful reconstruction of the polarized gluon PDF. We also expose the bias and problems with underestimating uncertainties associated with the use of model-dependent and overly constrained functional forms, such as $x^α(1-x)^β$ and its variants to extract PDFs from the lattice data. We propose the use of generative machine learning algorithms to mitigate these issues and present our determination of the polarized and unpolarized gluon PDFs in the nucleon.

hep-lat↗

arXiv2021

Pheno-Mapper: An Interactive Toolbox for the Visual Exploration of Phenomics Data

High-throughput technologies to collect field data have made observations possible at scale in several branches of life sciences. The data collected can range from the molecular level (genotypes) to physiological (phenotypic traits) and environmental observations (e.g., weather, soil conditions). These vast swathes of data, collectively referred to as phenomics data, represent a treasure trove of key scientific knowledge on the dynamics of the underlying biological system. However, extracting information and insights from these complex datasets remains a significant challenge owing to their multidimensionality and lack of prior knowledge about their complex structure. In this paper, we present Pheno-Mapper, an interactive toolbox for the exploratory analysis and visualization of large-scale phenomics data. Our approach uses the mapper framework to perform a topological analysis of the data, and subsequently render visual representations with built-in data analysis and machine learning capabilities. We demonstrate the utility of this new tool on real-world plant (e.g., maize) phenomics datasets. In comparison to existing approaches, the main advantage of Pheno-Mapper is that it provides rich, interactive capabilities in the exploratory analysis of phenomics data, and it integrates visual analytics with data analysis and machine learning in an easily extensible way. In particular, Pheno-Mapper allows the interactive selection of subpopulations guided by a topological summary of the data and applies data mining and machine learning to these selected subpopulations for in-depth exploration.

cs.CG↗

arXiv2019

Hyppo-X: A Scalable Exploratory Framework for Analyzing Complex Phenomics Data

Phenomics is an emerging branch of modern biology that uses high throughput phenotyping tools to capture multiple environmental and phenotypic traits, often at massive spatial and temporal scales. The resulting high dimensional data represent a treasure trove of information for providing an in-depth understanding of how multiple factors interact and contribute to the overall growth and behavior of different genotypes. However, computational tools that can parse through such complex data and aid in extracting plausible hypotheses are currently lacking. In this paper, we present Hyppo-X, a new algorithmic approach to visually explore complex phenomics data and in the process characterize the role of environment on phenotypic traits. We model the problem as one of unsupervised structure discovery, and use emerging principles from algebraic topology and graph theory for discovering higher-order structures of complex phenomics data. We present an open source software which has interactive visualization capabilities to facilitate data navigation and hypothesis formulation. We test and evaluate Hyppo-X on two real-world plant (maize) data sets. Our results demonstrate the ability of our approach to delineate divergent subpopulation-level behavior. Notably, our approach shows how environmental factors could influence phenotypic behavior, and how that effect varies across different genotypes and different time scales. To the best of our knowledge, this effort provides one of the first approaches to systematically formalize the problem of hypothesis extraction for phenomics data. Considering the infancy of the phenomics field, tools that help users explore complex data and extract plausible hypotheses in a data-guided manner will be critical to future advancements in the use of such data.

q-bio.QM↗

arXiv2018

Interesting Paths in the Mapper

The Mapper produces a compact summary of high dimensional data as a simplicial complex. We study the problem of quantifying the interestingness of subpopulations in a Mapper, which appear as long paths, flares, or loops. First, we create a weighted directed graph G using the 1-skeleton of the Mapper. We use the average values at the vertices of a target function to direct edges (from low to high). The difference between the average values at vertices (high-low) is set as the edge's weight. Covariation of the remaining h functions (independent variables) is captured by a h-bit binary signature assigned to the edge. An interesting path in G is a directed path whose edges all have the same signature. We define the interestingness score of such a path as a sum of its edge weights multiplied by a nonlinear function of their ranks in the path. Second, we study three optimization problems on this graph G. In the problem Max-IP, we seek an interesting path in G with the maximum interestingness score. We show that Max-IP is NP-complete. For the special case when G is a directed acyclic graph (DAG), we show that Max-IP can be solved in polynomial time - in O(mnd_i) where d_i is the maximum indegree of a vertex in G. In the more general problem IP, the goal is to find a collection of edge-disjoint interesting paths such that the overall sum of their interestingness scores is maximized. We also study a variant of IP termed k-IP, where the goal is to identify a collection of edge-disjoint interesting paths each with k edges, and their total interestingness score is maximized. While k-IP can be solved in polynomial time for k <= 2, we show k-IP is NP-complete for k >= 3 even when G is a DAG. We develop polynomial time heuristics for IP and k-IP on DAGs.

cs.CG↗