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Atmika Bhardwaj

Publications and source records attributed to Atmika Bhardwaj.

3 recordsLinked to original sources

Train, Test, Re-evaluate: Schedule-Sensitive Evaluation of Generative Data for Hand Detection

Generated (or synthetic) image data is increasingly used to augment or replace real training datasets when target imagery is scarce, expensive, or biased. For hand detection, particularly in occupational safety settings, public datasets mostly contain bare hands. This under-represents the variation in hand appearance introduced by gloves, tattoos, jewelry, and other personal protective equipment, creating a distribution shift that safety-critical applications encounter at deployment. We test whether generative inpainting, editing only the hand region of a real photograph to introduce accessories, can close this shift gap and improve detection of real hands at deployment. On a paired dataset of real images and their synthetic counterparts, we evaluate YOLOv8n hand detectors across six experiments (A-F), four of which involve training (A, C, D, E) under three random seeds each, evaluate them on a real test set and on a real-gloves-only test split, and report the mean average precision (mAP) at two overlap thresholds (mAP@0.5 and mAP@0.5:0.95) along with paired statistical tests. A two-stage experiment: train on real U synthetic data, then fine-tune the resulting weights on real-only at a lower learning rate, directionally improves mAP@0.5 compared to the real-only baseline model on the standard real test set, and narrows the real-gloves out-of-distribution gap. Another three-stage experiment preserves box-tightness best, achieving the highest mAP@0.5:0.95 among experiments in the study. The synthetic-data utility for safety-critical hand detection depends on the training procedure, and simple multi-stage experiments extract substantial real-deployment benefit from inpainted accessory data.

cs.CV

The Influence of Crosslinking and Deformation on Polymer Crystallization and Melting: A Molecular Dynamics Study

We investigate the crystallization of crosslinked and entangled polymers under external deformation using a coarse-grained poly(vinyl alcohol) (CG-PVA) model and molecular dynamics simulations. Following uniaxial deformation, the systems are cooled at a constant rate to form semi-crystalline states and subsequently heated at a constant rate to induce melting. For unstretched systems, network junctions do not significantly affect the nucleation temperature but increase the amorphous fraction and reduce the melting temperature. Uniaxial deformation accelerates nucleation and markedly increases the crystallization temperature, with more strongly crosslinked polymers exhibiting larger shifts that correlate with an enhanced orientation order parameter. We further compare cooling and heating cycles under constant-strain and constant-stress conditions. Under constant stress, crystallization induces additional elongation beyond the initial pre-stretch and leads to pronounced mechanical hysteresis upon heating, a behavior characteristic of reversible shape-memory materials.

cond-mat.soft

Nucleation patterns of polymer crystals analyzed by machine learning models

We use machine learning algorithms to detect the crystalline phase in undercooled melts in molecular dynamics simulations. Our classification method is based on local conformation and environmental fingerprints of individual monomers. In particular, we employ self-supervised auto-encoders to compress the fingerprint information and a Gaussian mixture model to distinguish ordered states from disordered ones. The resulting identification of crystalline monomers agrees to a large extent with human-defined classifiers such as the stem-length-based classification scheme as developed in our previous work [C. Luo and J.-U. Sommer, Macromolecules 44 (2011), 1523], but does not require any foreknowledge about the structure of semi-crystalline polymers. Because of its local sensitivity, the method allows the resolution of detailed time patterns of crystalline order before an apparent signature of the transition is visible in thermodynamic properties such as for the specific volume. At a pre-transition point, we observe the highest crystallization efficiency using the fraction of monomers being conserved in the crystalline phase as compared to the number of monomers joining that phase.

cond-mat.soft