Abstract
Nanomaterial-based aptasensors serve as useful instruments for detecting small biological entities. This work utilizes data gathered from three electrochemical aptamer-based sensors varying in receptors, analytes of interest, and lengths of signals. Our ultimate objective was the automatic detection and quantification of target analytes from a segment of the signal recorded by these sensors. Initially, we proposed a data augmentation method using conditional variational autoencoders to address data scarcity. Secondly, we employed recurrent-based networks for signal extrapolation, ensuring uniform signal lengths. In the third step, we developed seven deep learning classification models (GRU, unidirectional LSTM (ULSTM), bidirectional LSTM (BLSTM), ConvGRU, ConvULSTM, ConvBLSTM, and CNN) to identify and quantify specific analyte concentrations for six distinct classes, ranging from the absence of analyte to 10 μM. Finally, the second classification model was created to distinguish between abnormal and normal data segments, detect the presence or absence of analytes in the sample, and, if detected, identify the specific analyte and quantify its concentration. Evaluating the time series forecasting showed that the GRU-based network outperformed two other ULSTM and BLSTM networks. Regarding classification models, it turned out signal extrapolation was not effective in improving the classification performance. Comparing the role of the network architectures in classification performance, the result showed that hybrid networks, including both convolutional and recurrent layers and CNN networks, achieved 82% to 99% accuracy across all three datasets. Utilizing short-term Fourier transform (STFT) as the preprocessing technique improved the performance of all datasets with accuracies from 84% to 99%. These findings underscore the effectiveness of suitable data preprocessing methods in enhancing neural network performance, enabling automatic analyte identification and quantification from electrochemical aptasensor signals.