Abstract:This paper investigates multi-degrees of freedom (DoF) joint kinematics estimation under partially observed surface electromyography (sEMG), where only a subset of task-relevant muscles can be measured due to anatomical inaccessibility or sensor constraints. A novel musculoskeletal neural network (MSK-NN) is proposed to estimate multi-DoF joint angles while simultaneously inferring activations for both measured and unmeasured muscles. MSK-NN consists of a CNN-based muscle activation estimator and an embedded MSK forward dynamics module, forming a fully differentiable architecture. Unlike existing hybrid neural frameworks that require additional biomechanical labels (e.g., muscle-tendon forces, joint torques), MSK-NN is trained without direct supervision of internal biomechanical variables. A composite physics-physiology loss is designed by incorporating a joint kinematics loss, a data-driven muscle synergy loss, and an anatomy-guided trend loss. The proposed method is evaluated on two-DoF wrist kinematics estimation across three rhythmic motions with unconstrained speed and amplitude, and one random motion. Compared with CNN, Bi-LSTM, CNN-LSTM, and PET baselines, MSK-NN achieves lower normalized root mean square error (NRMSE) and higher coefficient of determination (R2), especially for the random motion. More importantly, the optimized MSK parameters remain within physiological limits, and the estimated activation of an input-excluded muscle exhibits strong temporal agreement with its recorded sEMG envelope, demonstrating the capability of musculoskeletal (MSK)-NN to recover physiologically plausible activations.
Abstract:Electrospinning is a scalable technique for producing fibrous scaffolds with tunable micro- and nanoscale architectures for applications in tissue engineering, drug delivery, and wound care. While machine learning (ML) has been used to support electrospinning process optimisation, most existing approaches predict only mean fibre diameters, neglecting the full diameter distribution that governs scaffold performance. This work presents FibreCastML, an open, distribution-aware ML framework that predicts complete fibre diameter spectra from routinely reported electrospinning parameters and provides interpretable insights into process structure relationships. A meta-dataset comprising 68538 individual fibre diameter measurements extracted from 1778 studies across 16 biomedical polymers was curated. Six standard processing parameters, namely solution concentration, applied voltage, flow rate, tip to collector distance, needle diameter, and collector rotation speed, were used to train seven ML models using nested cross validation with leave one study out external folds. Model interpretability was achieved using variable importance analysis, SHapley Additive exPlanations, correlation matrices, and three dimensional parameter maps. Non linear models consistently outperformed linear baselines, achieving coefficients of determination above 0.91 for several widely used polymers. Solution concentration emerged as the dominant global driver of fibre diameter distributions. Experimental validation across different electrospinning systems demonstrated close agreement between predicted and measured distributions. FibreCastML enables more reproducible and data driven optimisation of electrospun scaffold architectures.