A high-quality genome is the basis for studies on functional, evolutionary, and comparative genomics. The majority of attention has been paid to the solution of complex chromosome structures and highly repetitive sequences, along with the emergence of a new ‘telomere-to-telomere (T2T) assembly’ era. However, the bioinformatic tools for the automatic construction and/or characterization of T2T genome are limited. Here, we developed a user-friendly web toolkit, quarTeT, which currently includes four modules: AssemblyMapper, GapFiller, TeloExplorer, and CentroMiner. First, AssemblyMapper is designed to assemble phased contigs into the chromosome-level genome by referring to a closely related genome. Then, GapFiller would endeavor to fill all unclosed gaps in a given genome with the aid of additional ultra-long sequences. Finally, TeloExplorer and CentroMiner are applied to identify candidate telomere and centromere as well as their localizations on each chromosome. These four modules can be used alone or in combination with each other for T2T genome assembly and characterization. As a case study, by adopting the entire modular functions of quarTeT, we have achieved the Actinidia chinensis genome assembly that is of a quality comparable to the reported genome Hongyang v4.0, which was assembled with the addition of manual handling. Further evaluation of CentroMiner by searching centromeres in Arabidopsis thaliana and Oryza sativa genomes showed that quarTeT is capable of identifying all the centromeric regions that have been previously detected by experimental methods. Collectively, quarTeT is an efficient toolkit for studies of large-scale T2T genomes and can be accessed at http://www.atcgn.com:8080/quarTeT/home.html without registration.

Insect pests are a major element influencing agricultural production. According to the Food and Agriculture Organization (FAO), an estimated 20–40% of pest damage occurs each year, which reduces global production and becomes a major challenge to crop production. These insect pests cause sooty mold disease by sucking the sap from the crop’s organs, especially leaves, fruits, stems, and roots. To control these pests, pesticides are frequently used because they are fast-acting and scalable. Due to environmental pollution and health awareness, less use of pesticides is recommended. One of the salient approaches could be to reduce the wide use of pesticides by spraying on demand. To perform spot spraying, the location of the pest must first be determined. Therefore, the growing population and increasing food demand emphasize the development of novel methods and systems for agricultural production to address environmental concerns and ensure efficiency and sustainability. To accurately identify these insect pests at an early stage, insect pest detection and classification have recently become in high demand. Thus, this study aims to develop an object recognition system for the detection of crops damaging insect pests and their classification. The current work proposes an automatic system in the form of a smartphone IP- camera to detect insect pests from digital images/videos to reduce farmers’ reliance on pesticides. The proposed approach is based on YOLO object detection architectures including YOLOv5 (n, s, m, l, and x), YOLOv3, YOLO-Lite, and YOLOR. For this purpose, we collected 7046 images in the wild under different illumination and background conditions to train the underlying object detection approaches. We trained and test the object recognition system with different parameters from scratch. The eight models are compared and analyzed. The experimental results show that the average precision (AP@0.5) of the eight models including YOLO-Lite, YOLOv3, YOLOR, and YOLOv5 with five different scales (n, s, m, l, and x) reach 51.7%, 97.6%, 96.80%, 83.85%, 94.61%, 97.18%, 97.04%, and 98.3% respectively. The larger the model, the higher the average accuracy of the detection validation results. We observed that the YOLOv5x model is fully functional and can correctly identify the twenty-three species of insect pests at 40.5 milliseconds (ms). The developed model YOLOv5x performs the state-of-the-art model with an average precision value of (mAP@0.5) 98.3%, (mAP@0.5:0.95) value of 79.8%, precision of 94.5% and a recall of 97.8%, and F1-score with 96% on our IP-23 dataset. The results show that the system works efficiently and was able to correctly detect and identify insect pests, which can be employed for realistic application while farming.

Background: Over 200 published studies of more than 30 plant species have reported a role for miRNAs in regulating responses to abiotic stresses. However, data from these individual reports has not been collected into a single database. The lack of a curated database of stress-related miRNAs limits research in this field, and thus a cohesive database system should necessarily be constructed for data deposit and further application. Description: PASmiR, a literature-curated and web-accessible database, was developed to provide detailed, searchable descriptions of miRNA molecular regulation in different plant abiotic stresses. PASmiR currently includes data from ~200 published studies, representing 1038 regulatory relationships between 682 miRNAs and 35 abiotic stresses in 33 plant species. PASmiR’s interface allows users to retrieve miRNA-stress regulatory entries by keyword search using plant species, abiotic stress, and miRNA identifier. Each entry upon keyword query contains detailed regulation information for a specific miRNA, including species name, miRNA identifier, stress name, miRNA expression pattern, detection method for miRNA expression, a reference literature, and target gene(s) of the miRNA extracted from the corresponding reference or miRBase. Users can also contribute novel regulatory entries by using a web-based submission page. The PASmiR database is freely accessible from the two URLs of http://hi.ustc.edu.cn:8080/PASmiR, and http://pcsb.ahau.edu.cn:8080/PASmiR. Conclusion: The PASmiR database provides a solid platform for collection, standardization, and searching of miRNA-abiotic stress regulation data in plants. As such this database will be a comprehensive repository for miRNA regulatory mechanisms involved in plant response to abiotic stresses for the plant stress physiology community.

Background: Shotgun metagenomics based on untargeted sequencing can explore the taxonomic profile and the function of unknown microorganisms in samples, and complement the shortage of amplicon sequencing. Binning assembled sequences into individual groups, which represent microbial genomes, is the key step and a major challenge in metagenomic research. Both supervised and unsupervised machine learning methods have been employed in binning. Genome binning belonging to unsupervised method clusters contigs into individual genome bins by machine learning methods without the assistance of any reference databases. So far a lot of genome binning tools have emerged. Evaluating these genome tools is of great significance to microbiological research. In this study, we evaluate 15 genome binning tools containing 12 original binning tools and 3 refining binning tools by comparing the performance of these tools on chicken gut metagenomic datasets and the first CAMI challenge datasets.Results: For chicken gut metagenomic datasets, original genome binner MetaBat, Groopm2 and Autometa performed better than other original binner, and MetaWrap combined the binning results of them generated the most high-quality genome bins. For CAMI datasets, Groopm2 achieved the highest purity (> 0.9) with good completeness (> 0.8), and reconstructed the most high-quality genome bins among original genome binners. Compared with Groopm2, MetaBat2 had similar performance with higher completeness and lower purity. Genome refining binners DASTool predicated the most high-quality genome bins among all genomes binners. Most genome binner performed well for unique strains. Nonetheless, reconstructing common strains still is a substantial challenge for all genome binner.Conclusions: In conclusion, we tested a set of currently available, state-of-the-art metagenomics hybrid binning tools and provided a guide for selecting tools for metagenomic binning by comparing range of purity, completeness, adjusted rand index, and the number of high-quality reconstructed bins. Furthermore, available information for future binning strategy were concluded.

Background: Essential Proteins are demonstrated to exert vital functions on cellular processes and are indispensable for the survival and reproduction of the organism. Traditional centrality methods perform poorly on complex protein–protein interaction (PPI) networks. Machine learning approaches based on high-throughput data lack the exploitation of the temporal and spatial dimensions of biological information. Results: We put forward a deep learning framework to predict essential proteins by integrating features obtained from the PPI network, subcellular localization, and gene expression profiles. In our model, the node2vec method is applied to learn continuous feature representations for proteins in the PPI network, which capture the diversity of connectivity patterns in the network. The concept of depthwise separable convolution is employed on gene expression profiles to extract properties and observe the trends of gene expression over time under different experimental conditions. Subcellular localization information is mapped into a long one-dimensional vector to capture its characteristics. Additionally, we use a sampling method to mitigate the impact of imbalanced learning when training the model. With experiments carried out on the data of Saccharomyces cerevisiae, results show that our model outperforms traditional centrality methods and machine learning methods. Likewise, the comparative experiments have manifested that our process of various biological information is preferable. Conclusions: Our proposed deep learning framework effectively identifies essential proteins by integrating multiple biological data, proving a broader selection of subcellular localization information significantly improves the results of prediction and depthwise separable convolution implemented on gene expression profiles enhances the performance.

Image datasets acquired from orchards are commonly characterized by intricate backgrounds and an imbalanced distribution of disease categories, resulting in suboptimal recognition outcomes when attempting to identify apple leaf diseases. In this regard, we propose a novel apple leaf disease recognition model, named RFCA ResNet, equipped with a dual attention mechanism and multi-scale feature extraction capacity, to more effectively tackle these issues. The dual attention mechanism incorporated into RFCA ResNet is a potent tool for mitigating the detrimental effects of complex backdrops on recognition outcomes. Additionally, by utilizing the class balance technique in conjunction with focal loss, the adverse effects of an unbalanced dataset on classification accuracy can be effectively minimized. The RFB module enables us to expand the receptive field and achieve multi-scale feature extraction, both of which are critical for the superior performance of RFCA ResNet. Experimental results demonstrate that RFCA ResNet significantly outperforms the standard CNN network model, exhibiting marked improvements of 89.61%, 56.66%, 72.76%, and 58.77% in terms of accuracy rate, precision rate, recall rate, and F1 score, respectively. It is better than other approaches, performs well in generalization, and has some theoretical relevance and practical value.