We propose a blind identification method for multiple-input multiple-output (MIMO) single-carrier zero-padding block-transmission systems. The method uses periodic precoding on the source signal before transmission. The estimation of the channel impulse response matrix consists of two steps: 1) obtain the channel product matrix by solving a lower-triangular linear system; 2) obtain the channel impulse response matrix by computing the positive eigenvalues and eigenvectors of a Hermitian matrix formed from the channel product matrix. The method is applicable to MIMO channels with more transmitters or more receivers. A sufficient condition for identifiability is simply that the channel impulse response matrix is full column rank. The design of the precoding sequence which minimizes the noise effect in covariance matrix estimation is proposed and the effect of the optimal precoding sequence on channel equalization is discussed. Simulations are used to demonstrate the performance of the method.
1 September 2020 in Biomedical Signal Processing and Control
This article proposes a semiblind channel estimation method for multiple-input multiple-output orthogonal frequency-division multiplexing systems based on circular precoding. Relying on the precoding scheme at the transmitters, the autocorrelation matrix of the received data induces a structure relating the outer product of the channel frequency response matrix and precoding coefficients. This structure makes it possible to extract information about channel product matrices, which can be used to form a Hermitian matrix whose positive eigenvalues and corresponding eigenvectors yield the channel impulse response matrix. This article also tests the resistance of the precoding design to finite-sample estimation errors, and explores the effects of the precoding scheme on channel equalization by performing pairwise error probability analysis. The proposed method is immune to channel zero locations, and is reasonably robust to channel order overestimation. The proposed method is applicable to the scenarios in which the number of transmitters exceeds that of the receivers. Simulation results demonstrate the performance of the proposed method and compare it with some existing methods.
12 July 2012 in EURASIP Journal on Advances in Signal Processing
Background: Plantar pressure imaging is a stable modality that reflects gait-related biomechanical characteristics and has been used increasingly for gait assessment and recognition. However, plantar pressure images are high dimensional and nonlinear, making manual feature engineering and conventional machine learning insufficient to capture discriminative patterns. Objective: This study aimed to develop a gait pattern recognition model based on plantar pressure using an autoencoder (AE)-enhanced convolutional neural network (CNN) and to evaluate its performance against baseline deep learning and classical machine learning approaches. Methods: A total of 13 healthy volunteers (aged 18-24 years) were recruited. Plantar pressure data were collected during treadmill walking using an in-shoe pressure measurement system and converted into frame-wise plantar pressure images. We compared a lightweight CNN (Light CNN), an AE-CNN cascade model, and an encoder-augmented CNN with an additional bottleneck layer. Model development used participant-wise data partitioning, and performance was evaluated using accuracy, precision, recall, and F1-score. Results: The proposed encoder-augmented CNN achieved the best overall performance (F1-score=96.20%), outperforming the Light CNN (F1-score=94.44%) and AE-CNN cascade (F1-score=92.45%). Confusion matrices and learning curves further indicated stable training behavior and consistent classification performance across gait patterns. Conclusions: Integrating representation learning (AE-based compression) with CNN-based classification improved the recognition of gait patterns from plantar pressure images. This pilot study included only healthy participants. Future work should validate generalizability in larger and clinically diverse cohorts and further investigate participant-level evaluation and model interpretability, as well as deployment feasibility.