arXiv subjects

Aditya Sriram

Publications and source records attributed to Aditya Sriram.

9 recordsLinked to original sources

arXiv2026

Pinned Boundaries Delay Contraction and Shape Stress Relaxation in Active Gels

Cells dynamically generate, transmit, and dissipate stress. Central to these processes is the actomyosin cortex, an active contractile material that drives cellular mechanical behavior. While prior studies have focused on freely contracting actomyosin systems, the role of mechanical constraints such as adhesion to boundaries remains less explored. To address this, we employ reconstituted actomyosin gels to investigate cellular contractility. We study contraction dynamics under pinned boundary conditions, where the gel is adhered transversely to two opposing surfaces, mimicking supracellular actomyosin networks in tissues and embryos. We find that pinned contraction leads to stress buildup, delaying contraction, producing intermittent dynamics, and generating spatially nonuniform strain fields. Stress is relieved through several pathways, including active-stress-driven symmetric constriction and defect-driven processes such as boundary detachment and internal rupture. We develop a hydrodynamic model incorporating elastic, viscous, and active stress contributions that distinguishes between stress-accumulation and stress-release phases and links variations in active stress to the observed intermittent dynamics. The model predicts distinct energy relaxation rates before and after detachment events, providing insight into stress dissipation. We compare experiments with numerical simulations, which reproduce the observed behavior and reveal how internal energy is generated and dissipated during stress buildup and relaxation. Together, our results demonstrate how boundary conditions and spatial heterogeneity govern the mechanical behavior of contractile active gels. These findings provide insight into stress regulation in cellular and tissue-scale systems and may inform the design of adaptive soft materials and bioinspired robotic systems.

cond-mat.soft↗

arXiv2025

qa-FLoRA: Data-free query-adaptive Fusion of LoRAs for LLMs

The deployment of large language models for specialized tasks often requires domain-specific parameter-efficient finetuning through Low-Rank Adaptation (LoRA) modules. However, effectively fusing these adapters to handle complex, multi-domain composite queries remains a critical challenge. Existing LoRA fusion approaches either use static weights, which assign equal relevance to each participating LoRA, or require data-intensive supervised training for every possible LoRA combination to obtain respective optimal fusion weights. We propose qa-FLoRA, a novel query-adaptive data-and-training-free method for LoRA fusion that dynamically computes layer-level fusion weights by measuring distributional divergence between the base model and respective adapters. Our approach eliminates the need for composite training data or domain-representative samples, making it readily applicable to existing adapter collections. Extensive experiments across nine multilingual composite tasks spanning mathematics, coding, and medical domains, show that qa-FLoRA outperforms static fusion by ~5% with LLaMA-2 and ~6% with LLaMA-3, and the training-free baselines by ~7% with LLaMA-2 and ~10% with LLaMA-3, while significantly closing the gap with supervised baselines. Further, layer-level analysis of our fusion weights reveals interpretable fusion patterns, demonstrating the effectiveness of our approach for robust multi-domain adaptation.

cs.CL↗

arXiv2025

BARCODE: Biomaterial Activity Readouts to Categorize, Optimize, Design and Engineer for high throughput screening and characterization of dynamically restructuring soft materials

Active, responsive, nonequilibrium materials, at the forefront of materials engineering, offer dynamical restructuring, mobility and other complex life-like properties. Yet, this enhanced functionality comes with significant amplification of the size and complexity of the datasets needed to characterize their properties, thereby challenging conventional approaches to analysis. To meet this need, we present BARCODE (Biomaterial Activity Readouts to Categorize, Optimize, Design and Engineer), an open-access software that automates high throughput screening of microscopy video data to enable nonequilibrium material optimization and discovery. BARCODE produces a unique fingerprint or barcode of performance metrics that visually and quantitatively encodes dynamic material properties with minimal file size. Using three complementary material agnostic analysis branches, BARCODE significantly reduces data dimensionality and size, while providing rich, multiparametric outputs and rapid tractable characterization of activity and structure. We analyze a series of datasets of cytoskeleton networks and cell monolayers to demonstrate the ability of BARCODE to accelerate and streamline screening and analysis, reveal unexpected correlations and emergence, and enable broad non-expert data access, comparison, and sharing.

cond-mat.soft↗

arXiv2025

Active and passive crosslinking of cytoskeleton scaffolds tune the effects of cell inclusions on composite structure

Incorporating cells within active biomaterial scaffolds is a promising strategy to develop forefront materials that can autonomously sense, respond, and alter the scaffold in response to environmental cues or internal cell circuitry. Using dynamic biocompatible scaffolds that can self-alter their properties via crosslinking and motor-driven force-generation opens even greater avenues for actuation and control. However, the design principles associated with engineering active scaffolds embedded with cells are not well established. To address this challenge, we design a dynamic scaffold material of bacteria cells embedded within a composite cytoskeletal network of actin and microtubules that can be passively or actively crosslinked by either biotin-streptavidin or multimeric kinesin motors. Using quantitative microscopy, we demonstrate the ability to embed cells of volume fractions 0.4 to 2% throughout the network without compromising the structural integrity of the network or inhibiting crosslinking or motor-driven dynamics. Our findings suggest that both passive and active crosslinking promote entrainment of cells within the network, while depletion interactions play a more important role in uncrosslinked networks. Moreover, we show that large-scale structures emerge with the addition of cell fractions as low as 0.4%, but these structures do not influence the microscale structural lengthscale of the materials. Our work highlights the potential of our composite biomaterial in designing autonomous materials controlled by cells, and provides a roadmap for effectively coupling cells to complex composite materials with an eye towards using cells as in situ factories to program material modifications.

physics.bio-ph↗

arXiv2020

Forming Local Intersections of Projections for Classifying and Searching Histopathology Images

In this paper, we propose a novel image descriptor called Forming Local Intersections of Projections (FLIP) and its multi-resolution version (mFLIP) for representing histopathology images. The descriptor is based on the Radon transform wherein we apply parallel projections in small local neighborhoods of gray-level images. Using equidistant projection directions in each window, we extract unique and invariant characteristics of the neighborhood by taking the intersection of adjacent projections. Thereafter, we construct a histogram for each image, which we call the FLIP histogram. Various resolutions provide different FLIP histograms which are then concatenated to form the mFLIP descriptor. Our experiments included training common networks from scratch and fine-tuning pre-trained networks to benchmark our proposed descriptor. Experiments are conducted on the publicly available dataset KIMIA Path24 and KIMIA Path960. For both of these datasets, FLIP and mFLIP descriptors show promising results in all experiments.Using KIMIA Path24 data, FLIP outperformed non-fine-tuned Inception-v3 and fine-tuned VGG16 and mFLIP outperformed fine-tuned Inception-v3 in feature extracting.

cs.CV↗

arXiv2019

Projectron -- A Shallow and Interpretable Network for Classifying Medical Images

This paper introduces the `Projectron' as a new neural network architecture that uses Radon projections to both classify and represent medical images. The motivation is to build shallow networks which are more interpretable in the medical imaging domain. Radon transform is an established technique that can reconstruct images from parallel projections. The Projectron first applies global Radon transform to each image using equidistant angles and then feeds these transformations for encoding to a single layer of neurons followed by a layer of suitable kernels to facilitate a linear separation of projections. Finally, the Projectron provides the output of the encoding as an input to two more layers for final classification. We validate the Projectron on five publicly available datasets, a general dataset (namely MNIST) and four medical datasets (namely Emphysema, IDC, IRMA, and Pneumonia). The results are encouraging as we compared the Projectron's performance against MLPs with raw images and Radon projections as inputs, respectively. Experiments clearly demonstrate the potential of the proposed Projectron for representing/classifying medical images.

cs.CV↗

arXiv2017

Learning Autoencoded Radon Projections

Autoencoders have been recently used for encoding medical images. In this study, we design and validate a new framework for retrieving medical images by classifying Radon projections, compressed in the deepest layer of an autoencoder. As the autoencoder reduces the dimensionality, a multilayer perceptron (MLP) can be employed to classify the images. The integration of MLP promotes a rather shallow learning architecture which makes the training faster. We conducted a comparative study to examine the capabilities of autoencoders for different inputs such as raw images, Histogram of Oriented Gradients (HOG) and normalized Radon projections. Our framework is benchmarked on IRMA dataset containing $14,410$ x-ray images distributed across $57$ different classes. Experiments show an IRMA error of $313$ (equivalent to $\approx 82\%$ accuracy) outperforming state-of-the-art works on retrieval from IRMA dataset using autoencoders.

cs.CV↗

arXiv2017

Classification and Retrieval of Digital Pathology Scans: A New Dataset

In this paper, we introduce a new dataset, \textbf{Kimia Path24}, for image classification and retrieval in digital pathology. We use the whole scan images of 24 different tissue textures to generate 1,325 test patches of size 1000$\times$1000 (0.5mm$\times$0.5mm). Training data can be generated according to preferences of algorithm designer and can range from approximately 27,000 to over 50,000 patches if the preset parameters are adopted. We propose a compound patch-and-scan accuracy measurement that makes achieving high accuracies quite challenging. In addition, we set the benchmarking line by applying LBP, dictionary approach and convolutional neural nets (CNNs) and report their results. The highest accuracy was 41.80\% for CNN.

cs.CV↗

arXiv2016

Learning Opposites Using Neural Networks

Many research works have successfully extended algorithms such as evolutionary algorithms, reinforcement agents and neural networks using "opposition-based learning" (OBL). Two types of the "opposites" have been defined in the literature, namely \textit{type-I} and \textit{type-II}. The former are linear in nature and applicable to the variable space, hence easy to calculate. On the other hand, type-II opposites capture the "oppositeness" in the output space. In fact, type-I opposites are considered a special case of type-II opposites where inputs and outputs have a linear relationship. However, in many real-world problems, inputs and outputs do in fact exhibit a nonlinear relationship. Therefore, type-II opposites are expected to be better in capturing the sense of "opposition" in terms of the input-output relation. In the absence of any knowledge about the problem at hand, there seems to be no intuitive way to calculate the type-II opposites. In this paper, we introduce an approach to learn type-II opposites from the given inputs and their outputs using the artificial neural networks (ANNs). We first perform \emph{opposition mining} on the sample data, and then use the mined data to learn the relationship between input $x$ and its opposite $\breve{x}$. We have validated our algorithm using various benchmark functions to compare it against an evolving fuzzy inference approach that has been recently introduced. The results show the better performance of a neural approach to learn the opposites. This will create new possibilities for integrating oppositional schemes within existing algorithms promising a potential increase in convergence speed and/or accuracy.

cs.LG↗