Kei Hang Katie Chan | Searcharxiv

arXiv2023

DPCIPI: A pre-trained deep learning model for predicting cross-immunity between drifted strains of Influenza A/H3N2

Predicting cross-immunity between viral strains is vital for public health surveillance and vaccine development. Traditional neural network methods, such as BiLSTM, could be ineffective due to the lack of lab data for model training and the overshadowing of crucial features within sequence concatenation. The current work proposes a less data-consuming model incorporating a pre-trained gene sequence model and a mutual information inference operator. Our methodology utilizes gene alignment and deduplication algorithms to preprocess gene sequences, enhancing the model's capacity to discern and focus on distinctions among input gene pairs. The model, i.e., DNA Pretrained Cross-Immunity Protection Inference model (DPCIPI), outperforms state-of-the-art (SOTA) models in predicting hemagglutination inhibition titer from influenza viral gene sequences only. Improvement in binary cross-immunity prediction is 1.58% in F1, 2.34% in precision, 1.57% in recall, and 1.57% in Accuracy. For multilevel cross-immunity improvements, the improvement is 2.12% in F1, 3.50% in precision, 2.19% in recall, and 2.19% in Accuracy. Our study highlights the potential of pre-trained gene models in revolutionizing gene sequence-related prediction tasks. With more gene sequence data being harnessed and larger models trained, we foresee a significant impact of pre-trained models on clinical and public health applications.

cs.CE↗

arXiv2021

Identifying Autism Spectrum Disorder Based on Individual-Aware Down-Sampling and Multi-Modal Learning

Autism Spectrum Disorder(ASD) is a set of neurodevelopmental conditions that affect patients' social abilities. In recent years, many studies have employed deep learning to diagnose this brain dysfunction through functional MRI (fMRI). However, existing approaches solely focused on the abnormal brain functional connections but ignored the impact of regional activities. Due to this biased prior knowledge, previous diagnosis models suffered from inter-site measurement heterogeneity and inter-individual phenotypic differences. To address this issue, we propose a novel feature extraction method for fMRI that can learn a personalized lower-resolution representation of the entire brain networking regarding both the functional connections and regional activities. Specifically, we abstract the brain imaging as a graph structure and straightforwardly downsample it to substructures by hierarchical graph pooling. To further recalibrate the distribution of the extracted features under phenotypic information, we subsequently embed the sparse feature vectors into a population graph, where the hidden inter-subject heterogeneity and homogeneity are explicitly expressed as inter- and intra-community connectivity differences, and utilize Graph Convolutional Networks to learn the node embeddings. By these means, our framework can extract features directly and efficiently from the entire fMRI and be aware of implicit inter-individual variance. We have evaluated our framework on the ABIDE-I dataset with 10-fold cross-validation. The present model has achieved a mean classification accuracy of 87.62\% and a mean AUC of 0.92, better than the state-of-the-art methods.

eess.IV↗