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Connections between circular RNAs (circRNAs) and microRNAs (miRNAs) assume a pivotal position in the onset, evolution, diagnosis and treatment of diseases and tumors. Selecting the most potential circRNA-related miRNAs and taking advantage of them as the biological markers or drug targets could be conducive to dealing with complex human diseases through preventive strategies, diagnostic procedures and therapeutic approaches. Compared to traditional biological experiments, leveraging computational models to integrate diverse biological data in order to infer potential associations proves to be a more efficient and cost-effective approach. This paper developed a model of Convolutional Autoencoder for CircRNA–MiRNA Associations (CA-CMA) prediction. Initially, this model merged the natural language characteristics of the circRNA and miRNA sequence with the features of circRNA–miRNA interactions. Subsequently, it utilized all circRNA–miRNA pairs to construct a molecular association network, which was then fine-tuned by labeled samples to optimize the network parameters. Finally, the prediction outcome is obtained by utilizing the deep neural networks classifier. This model innovatively combines the likelihood objective that preserves the neighborhood through optimization, to learn the continuous feature representation of words and preserve the spatial information of two-dimensional signals. During the process of 5-fold cross-validation, CA-CMA exhibited exceptional performance compared to numerous prior computational approaches, as evidenced by its mean area under the receiver operating characteristic curve of 0.9138 and a minimal SD of 0.0024. Furthermore, recent literature has confirmed the accuracy of 25 out of the top 30 circRNA–miRNA pairs identified with the highest CA-CMA scores during case studies. The results of these experiments highlight the robustness and versatility of our model. [ABSTRACT FROM AUTHOR]

Despite the great efforts to find an effective way for coronavirus disease 2019 (COVID-19) prediction, the virus nature and mutation represent a critical challenge to diagnose the covered cases. However, developing a model to predict COVID-19 via chest X-ray images with accurate performance is necessary to help in early diagnosis. In this paper, a hybrid quantum-classical convolutional neural network (HQ-CNN) model using random quantum circuits as a base to detect COVID-19 patients with chest X-ray images is presented. A collection of 5445 chest X-ray images, including 1350 COVID-19, 1350 normal, 1345 viral pneumonia, and 1400 bacterial pneumonia images, were used to evaluate the HQ-CNN. The proposed HQ-CNN model has achieved higher performance with an accuracy of 98.6% and a recall of 99% on the first experiment (COVID-19 and normal cases). Besides, it obtained an accuracy of 98.2% and a recall of 99.5% on the second experiment (COVID-19 and viral pneumonia cases). Also, it obtained 98% and 98.8% for accuracy and recall, respectively, on the third dataset (COVID-19 and bacterial pneumonia cases). Lastly, it achieved accuracy and recall of 88.2% and 88.6%, respectively, on the multiclass dataset cases. Moreover, the HQ-CNN model is assessed with the statistical analysis (i.e. Cohen's Kappa and Matthew correlation coefficients). The experimental results revealed that the proposed HQ-CNN model is able to predict the positive COVID-19 cases. [ABSTRACT FROM AUTHOR]

T-cell receptors (TCRs) play an essential role in the adaptive immune system. Probabilistic models for TCR repertoires can help decipher the underlying complex sequence patterns and provide novel insights into understanding the adaptive immune system. In this work, we develop TCRpeg, a deep autoregressive generative model to unravel the sequence patterns of TCR repertoires. TCRpeg largely outperforms state-of-the-art methods in estimating the probability distribution of a TCR repertoire, boosting the average accuracy from 0.672 to 0.906 measured by the Pearson correlation coefficient. Furthermore, with promising performance in probability inference, TCRpeg improves on a range of TCR-related tasks: profiling TCR repertoire probabilistically, classifying antigen-specific TCRs, validating previously discovered TCR motifs, generating novel TCRs and augmenting TCR data. Our results and analysis highlight the flexibility and capacity of TCRpeg to extract TCR sequence information, providing a novel approach for deciphering complex immunogenomic repertoires. [ABSTRACT FROM AUTHOR]

Accurate identification of genetic variants from family child–mother–father trio sequencing data is important in genomics. However, state-of-the-art approaches treat variant calling from trios as three independent tasks, which limits their calling accuracy for Nanopore long-read sequencing data. For better trio variant calling, we introduce Clair3-Trio, the first variant caller tailored for family trio data from Nanopore long-reads. Clair3-Trio employs a Trio-to-Trio deep neural network model, which allows it to input the trio sequencing information and output all of the trio's predicted variants within a single model to improve variant calling. We also present MCVLoss, a novel loss function tailor-made for variant calling in trios, leveraging the explicit encoding of the Mendelian inheritance. Clair3-Trio showed comprehensive improvement in experiments. It predicted far fewer Mendelian inheritance violation variations than current state-of-the-art methods. We also demonstrated that our Trio-to-Trio model is more accurate than competing architectures. Clair3-Trio is accessible as a free, open-source project at https://github.com/HKU-BAL/Clair3-Trio. [ABSTRACT FROM AUTHOR]