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Biology subjects

Jadhav, J.

Publications and source records attributed to Jadhav, J..

2 recordsLinked to original sources

Ensemble-Based Deep Learning for Breast Cancer Detection and Classification in Histopathological Images

Breast cancer remains one of the leading causes of cancer-related mortality worldwide, with early detection being crucial for improved patient outcomes. This paper presents a comprehensive deep learning framework for automated breast cancer detection in histopathological images, incorporating advanced preprocessing techniques, enhanced segmentation methods, and multi-architecture ensemble classification. Our methodology employs a systematic approach using the BreakHis dataset with rigorous experimental design to ensure unbiased evaluation. The framework integrates Fast Non-Local Means denoising, Wiener filtering, and U-Net based segmentation for optimal image preprocessing, followed by feature extraction from multiple categories including statistical, texture, and morphological features. We evaluate 18 state-of-the-art convolutional neural network architectures and implement advanced ensemble methods for superior classification performance. Our results demonstrate exceptional performance with the best individual model achieving 98.90% accuracy, while ensemble methods reach 99.45% accuracy through confidence-based fusion. The framework provides comprehensive interpretability through Grad-CAM visualizations and statistical validation using McNemars test and medical diagnostic metrics. This work represents a significant advancement in computational pathology, offering a robust and clinically viable solution for automated breast cancer diagnosis with enhanced accuracy and reliability.

bioengineering↗

Slit1 -a MET target gene in the embryonic limbs, prevents premature differentiation during mammalian myogenesis.

Skeletal myogenesis requires precise spatio-temporal regulation of molecular signals during prenatal and postnatal development. Prenatal myogenesis in mouse commences at embryonic day (E) 9.5, characterized by the expression of PAX3 -a key myogenic regulator, and its target MET, in the embryonic muscle progenitor cells (EMPCs). These EMPCs delaminate from dermomyotome in the somites and migrate to designated areas such as the developing embryonic limbs and diaphragm. The trajectory of their migration is directed and limited by spatio-temporal availability of the MET ligand (HGF). Given its periodic expression during embryonic myogenesis and its recent association with familial arthrogryposis, it is important to identify additional non-migratory functions of MET signaling. We find conditional loss of Met in the Pax3/somitic lineage affects survival in early neonatal stages because amuscular diaphragms cause respiratory distress. Impaired progenitor migration in conditional Met knockouts (cMetKO) results in highly dysplastic muscles in neonates compared to muscleless limbs observed in previous mutants. Additionally, using cMetKO embryos (E11.5) we identify Slit1 as a novel target of MET that is downregulated in the mutant limb buds. Pharmacological modulation with SU11274, in vitro, confirms Slit1 as a MET responsive gene, which if knocked down in myoblasts leads to precocious myogenic differentiation. Similarly, cMetKO embryos, having reduced Slit1 expression, show greater myotomal differentiation and compact organization, compared to wildtype embryos. While Slit1 emerges as a MET target that represses precocious switch to myogenic differentiation, molecular intricacies of MET-mediated regulation of Slit1 and their spatio-temporal dynamic in fine-tuning myogenesis in the nascent limbs needs further examination.

developmental biology↗