Mohit Jindal

Sunny Gupta, Mohit Jindal, Pankhi Kashyap et al.

Federated learning faces a critical challenge in balancing communication efficiency with rapid convergence, especially for second-order methods. While Newton-type algorithms achieve linear convergence in communication rounds, transmitting full Hessian matrices is often impractical due to quadratic complexity. We introduce Federated Learning with Enhanced Nesterov-Newton Sketch (FLeNS), a novel method that harnesses both the acceleration capabilities of Nesterov's method and the dimensionality reduction benefits of Hessian sketching. FLeNS approximates the centralized Newton's method without relying on the exact Hessian, significantly reducing communication overhead. By combining Nesterov's acceleration with adaptive Hessian sketching, FLeNS preserves crucial second-order information while preserving the rapid convergence characteristics. Our theoretical analysis, grounded in statistical learning, demonstrates that FLeNS achieves super-linear convergence rates in communication rounds - a notable advancement in federated optimization. We provide rigorous convergence guarantees and characterize tradeoffs between acceleration, sketch size, and convergence speed. Extensive empirical evaluation validates our theoretical findings, showcasing FLeNS's state-of-the-art performance with reduced communication requirements, particularly in privacy-sensitive and edge-computing scenarios. The code is available at https://github.com/sunnyinAI/FLeNS

Ravi Kant Gupta, Mohit Jindal, Garima Jain et al.

We address the challenge of automated classification of diffuse large B-cell lymphoma (DLBCL) into its two primary subtypes: activated B-cell-like (ABC) and germinal center B-cell-like (GCB). Accurate classification between these subtypes is essential for determining the appropriate therapeutic strategy, given their distinct molecular profiles and treatment responses. Our proposed deep learning model demonstrates robust performance, achieving an average area under the curve (AUC) of (87.4 pm 5.7)\% during cross-validation. It shows a high positive predictive value (PPV), highlighting its potential for clinical application, such as triaging for molecular testing. To gain biological insights, we performed an analysis of morphological features of ABC and GCB subtypes. We segmented cell nuclei using a pre-trained deep neural network and compared the statistics of geometric and color features for ABC and GCB. We found that the distributions of these features were not very different for the two subtypes, which suggests that the visual differences between them are more subtle. These results underscore the potential of our method to assist in more precise subtype classification and can contribute to improved treatment management and outcomes for patients of DLBCL.