Trisomy 21 results in Down syndrome, a multifaceted genetic disorder with diverse clinical phenotypes, including heart defects, immune dysfunction, neurodevelopmental differences, and early-onset dementia risk. Heterogeneity and fragmented data across studies challenge comprehensive research and translational discovery. The NIH INCLUDE (INvestigation of Co-occurring conditions across the Lifespan to Understand Down syndromE) initiative has assembled harmonized participant-level datasets, yet realizing their potential requires integrative analytical frameworks. We developed a knowledge graph-driven platform transforming nine INCLUDE studies, comprising 7,148 participants, 456 conditions, 501 phenotypes, and over 37,000 biospecimens, into a unified semantic infrastructure. Cross-resource enrichment with Monarch Initiative data expands coverage to 4,281 genes and 7,077 variants. The resulting knowledge graph contains over 1.6 million semantic associations, enabling AI-ready analysis with graph embeddings and path-based reasoning for hypothesis generation. Researchers can query the graph via SPARQL or natural language interfaces. This framework converts static data repositories into dynamic discovery environments, supporting cross-study pattern recognition, predictive modeling, and systematic exploration of genotype-phenotype relationships in Down syndrome.

Advanced bioimaging technologies have enabled the large-scale acquisition of multidimensional data, yet effective metadata management and interoperability remain significant challenges. To address these issues, we propose a new ontology-driven framework for the Systems Science of Biological Dynamics Database (SSBD) that adopts a two-tier architecture. The core layer provides a class-centric structure referencing existing biomedical ontologies, supporting both SSBD:repository -- which focuses on rapid dataset publication with minimal metadata -- and SSBD:database, which is enhanced with biological and imaging-related annotations. Meanwhile, the instance layer represents actual imaging dataset information as Resource Description Framework individuals that are explicitly linked to the core classes. This layered approach aligns flexible instance data with robust ontological classes, enabling seamless integration and advanced semantic queries. By coupling flexibility with rigor, the SSBD Ontology promotes interoperability, data reuse, and the discovery of novel biological mechanisms. Moreover, our solution aligns with the Recommended Metadata for Biological Images guidelines and fosters compatibility. Ultimately, our approach contributes to establishing a Findable, Accessible, Interoperable, and Reusable data ecosystem within the bioimaging community.

D rug discovery requires a tremendous amount of time and cost. Computational drug - target interaction prediction, a n important part of this process, can reduce these requirements by narrowing the search space for wet lab experiments. In this survey, we provid e comprehensive details of graph machine learning - based methods in predicting drug - target interaction, as they have shown promising results in this field. These details include the overall framework, main contribution, dataset s, and their source code s . The selected papers were mainly published from 2020 to 2024 . Prior to discussing papers, we briefly introduce the datasets commonly used with these methods and measurements to assess their performance. Finally, future challenges and some crucial areas that need to be explored are discussed.

Given usefulness of protein language models (LMs) in structure and functional inference, RNA LMs have received increased attentions in the last few years. However, these RNA models are often not compared against the same standard. Here, we divided RNA LMs into three classes (pretrained on multiple RNA types (especially noncoding RNAs), specific-purpose RNAs, and LMs that unify RNA with DNA or proteins or both) and compared 13 RNA LMs along with 3 DNA and 1 protein LMs as controls in zero-shot prediction of RNA secondary structure and functional classification. Results shows that the models doing well on secondary structure prediction often perform worse in function classification or vice versa, suggesting that more balanced unsupervised training is needed.

Deep learning-based drug-target interaction (DTI) prediction methods have demonstrated strong performance; however, real-world applicability remains constrained by limited data diversity and modeling complexity. To address these challenges, we propose SCOPE-DTI, a unified framework combining a large-scale, balanced semi-inductive human DTI dataset with advanced deep learning modeling. Constructed from 13 public repositories, the SCOPE dataset expands data volume by up to 100-fold compared to common benchmarks such as the Human dataset. The SCOPE model integrates three-dimensional protein and compound representations, graph neural networks, and bilinear attention mechanisms to effectively capture cross domain interaction patterns, significantly outperforming state-of-the-art methods across various DTI prediction tasks. Additionally, SCOPE-DTI provides a user-friendly interface and database. We further validate its effectiveness by experimentally identifying anticancer targets of Ginsenoside Rh1. By offering comprehensive data, advanced modeling, and accessible tools, SCOPE-DTI accelerates drug discovery research.

The work presented in this paper makes three scientific contributions with a specific focus on mining and analysis of COVID-19-related posts on Instagram. First, it presents a multilingual dataset of 500,153 Instagram posts about COVID-19 published between January 2020 and September 2024. This dataset, available at https://dx.doi.org/10.21227/d46p-v480, contains Instagram posts in 161 different languages as well as 535,021 distinct hashtags. After the development of this dataset, multilingual sentiment analysis was performed, which involved classifying each post as positive, negative, or neutral. The results of sentiment analysis are presented as a separate attribute in this dataset. Second, it presents the results of performing sentiment analysis per year from 2020 to 2024. The findings revealed the trends in sentiment related to COVID-19 on Instagram since the beginning of the pandemic. For instance, between 2020 and 2024, the sentiment trends show a notable shift, with positive sentiment decreasing from 38.35% to 28.69%, while neutral sentiment rising from 44.19% to 58.34%. Finally, the paper also presents findings of language-specific sentiment analysis. This analysis highlighted similar and contrasting trends of sentiment across posts published in different languages on Instagram. For instance, out of all English posts, 49.68% were positive, 14.84% were negative, and 35.48% were neutral. In contrast, among Hindi posts, 4.40% were positive, 57.04% were negative, and 38.56% were neutral, reflecting distinct differences in the sentiment distribution between these two languages.

The prediction of intrinsic disorder regions has significant implications for understanding protein functions and dynamics. It can help to discover novel protein-protein interactions essential for designing new drugs and enzymes. Recently, a new generation of predictors based on protein language models (pLMs) is emerging. These algorithms reach state-of-the-art accuracy with-out calculating time-consuming multiple sequence alignments (MSAs). The article introduces the new DisorderUnetLM disorder predictor, which builds upon the idea of ProteinUnet. It uses the Attention U-Net convolutional neural network and incorporates features from the ProtTrans pLM. DisorderUnetLM achieves top results in the direct comparison with recent predictors exploiting MSAs and pLMs. Moreover, among 43 predictors from the latest CAID-2 benchmark, it ranks 1st for the Disorder-NOX subset (ROC-AUC of 0.844) and 10th for the Disorder-PDB subset (ROC-AUC of 0.924). The code and model are publicly available and fully reproducible at doi.org/10.24433/CO.7350682.v1.

We introduce a novel fully convolutional neural network (FCN) architecture for predicting the secondary structure of ribonucleic acid (RNA) molecules. Interpreting RNA structures as weighted graphs, we employ deep learning to estimate the probability of base pairing between nucleotide residues. Unique to our model are its massive 11-pixel kernels, which we argue provide a distinct advantage for FCNs on the specialized domain of RNA secondary structures. On a widely adopted, standardized test set comprised of 1,305 molecules, the accuracy of our method exceeds that of current state-of-the-art (SOTA) secondary structure prediction software, achieving a Matthews Correlation Coefficient (MCC) over 11-40% higher than that of other leading methods on overall structures and 58-400% higher on pseudoknots specifically.

Creating knowledge bases and ontologies is a time consuming task that relies on a manual curation. AI/NLP approaches can assist expert curators in populating these knowledge bases, but current approaches rely on extensive training data, and are not able to populate arbitrary complex nested knowledge schemas. Here we present Structured Prompt Interrogation and Recursive Extraction of Semantics (SPIRES), a Knowledge Extraction approach that relies on the ability of Large Language Models (LLMs) to perform zero-shot learning (ZSL) and general-purpose query answering from flexible prompts and return information conforming to a specified schema. Given a detailed, user-defined knowledge schema and an input text, SPIRES recursively performs prompt interrogation against GPT-3+ to obtain a set of responses matching the provided schema. SPIRES uses existing ontologies and vocabularies to provide identifiers for all matched elements. We present examples of use of SPIRES in different domains, including extraction of food recipes, multi-species cellular signaling pathways, disease treatments, multi-step drug mechanisms, and chemical to disease causation graphs. Current SPIRES accuracy is comparable to the mid-range of existing Relation Extraction (RE) methods, but has the advantage of easy customization, flexibility, and, crucially, the ability to perform new tasks in the absence of any training data. This method supports a general strategy of leveraging the language interpreting capabilities of LLMs to assemble knowledge bases, assisting manual knowledge curation and acquisition while supporting validation with publicly-available databases and ontologies external to the LLM. SPIRES is available as part of the open source OntoGPT package: https://github.com/ monarch-initiative/ontogpt.

The "RNA world" represents a novel frontier for the study of fundamental biological processes and human diseases and is paving the way for the development of new drugs tailored to the patient's biomolecular characteristics. Although scientific data about coding and non-coding RNA molecules are continuously produced and available from public repositories, they are scattered across different databases and a centralized, uniform, and semantically consistent representation of the "RNA world" is still lacking. We propose RNA-KG, a knowledge graph encompassing biological knowledge about RNAs gathered from more than 50 public databases, integrating functional relationships with genes, proteins, and chemicals and ontologically grounded biomedical concepts. To develop RNA-KG, we first identified, pre-processed, and characterized each data source; next, we built a meta-graph that provides an ontological description of the KG by representing all the bio-molecular entities and medical concepts of interest in this domain, as well as the types of interactions connecting them. Finally, we leveraged an instance-based semantically abstracted knowledge model to specify the ontological alignment according to which RNA-KG was generated. RNA-KG can be downloaded in different formats and also queried by a SPARQL endpoint. A thorough topological analysis of the resulting heterogeneous graph provides further insights into the characteristics of the "RNA world". RNA-KG can be both directly explored and visualized, and/or analyzed by applying computational methods to infer bio-medical knowledge from its heterogeneous nodes and edges. The resource can be easily updated with new experimental data, and specific views of the overall KG can be extracted according to the bio-medical problem to be studied.