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Identification and analysis of DEGs of mouse tumor cells by integrated bioinformatics methods

Mutations and genome instability are hallmarks of cancer. The advanced Next Generation Sequencing(NGS) technology now enables rapid and cost-effective analysis for tumoral and normal genomic translational research. In this research, mRNA sequencing was applied to get the whole transcriptome data of mouse B16F10 melanoma and CT26 colon carcinoma cells. Up regulation genes and down regulation genes were identified in tumor cells with differentially expressed genes(DEGs) analysis. The DEGs were analyzed with GO, KEGG and Reactome pathway enrichment study. Results demonstrated the DEGs and enriched pathways were mainly associated with cell proliferation and biosynthetic processing. Further, gene fusion and alternative splicing analysis reveled fusion genes and skipped exons were extensive exist within the chromosomes of tumor cells. Together, the integrated DEGs and bioinformatics analysis in this article may shed light on further research of cancer treating targets and molecular mechanisms of carcinogenesis.

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A Bioinformatics-Driven ceRNA Network in Stomach Adenocarcinoma: Identification of Novel Prognostic mRNA-miRNA-lncRNA Interactions

Stomach adenocarcinoma is a major contributor to worldwide mortality and poses a substantial challenge to improving life expectancy. The main objective of the current work was to identify diagnostic and prognostic biomarkers in stomach adenocarcinoma in order to advance translational medicine and patient outcomes. By accomplishing this objective, the research seeks to provide significant insights into the field of translational medicine. Seven novel unfavourable prognosis-associated genes (NALCN, CALCR, CPT1C, ELAVL3, FLJ16779, MYOZ3, and TPST1) were first identified. Additionally, 41 potential miRNAs were predicted. ELAVL3-hsa-mir-29a-3p and CALCR-hsa-mir-29a-3p axes were identified as two critical pathways in the carcinogenesis of stomach adenocarcinoma via a bioinformatics analysis. Following that, lncRNAs binding to hsa-mir-29a-3p were predicted via starBase and miRNet databases for predicting lncRNA binding sites. After conducting both expression and survival analyses for these predicted lncRNAs, we found that only one lncRNA (KCNQ1OT1) was markedly overexpressed in stomach adenocarcinoma, and its elevated expression was associated with an unfavourable prognosis. Next, we established a comprehensive mRNA-miRNA-lncRNA triple ceRNA network linked to the prognosis of patients with stomach adenocarcinoma. In summary, the current study provides an extensive ceRNA network that highlights novel diagnostic and prognostic biomarkers for stomach adenocarcinoma.

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Bioinformatics Analysis of Non-Coding UTR Variants in STAT1 Reveals Disruption of miRNA Binding, mRNA Stability, and Oncogenic Potential

Single nucleotide polymorphisms (SNPs) are associated with a wide range of disorders, including diverse cancer types. In the context of cancer, alterations within non-coding regions, specifically untranslated regions (UTRs), have proven substantially important. SNPs localized in the 3 prime UTRs of the STAT1 gene were assessed for their association with miRNAs using PolymiRTS, miRNASNP, and MicroSNIper. In addition, the 5 UTR SNPs were analyzed by SNP INFO for changes in the transcription factors binding sites. The significant SNPs were further analysed by Cscape to predict their oncogenic probability. The secondary structures of the wild type and the mutant mRNA were analysed by RNAfold. Out of 605 SNPs analyzed, 14 UTR SNPs (six in the 3 UTR region and eight in the 5 UTR region) were identified with functional annotation [≤]2a by RegulomeDB. The associations of 8 SNPs with miRNAs common between the 3 databases (PolymiRTS, miRNASNP, and MicroSNIper) were found. Moreover we identified six SNPs (rs1197872838, rs3088307, rs45470392, rs1413522785, rs531009254, and rs190508584) destabilize the mRNA structure resulting in substantial change in free energy ({Delta}G). The SNP rs45470392 in 5 UTR was predicted to alter the transcription factor binding sites. rs188557905, rs1220766131, rs1413522785, rs1168, and rs999207177 were predicted to be oncogenic SNPs in this study using bioinformatics tools. Our findings highlight the impact of 3 and 5 UTR SNPs on miRNA, transcription, and translation of STAT1. These analyses suggest that these SNPs can have substantial functional importance in the STAT1 gene. Future experimental validation could establish their potential role in the diagnosis and therapeutics of various diseases, including cancer.

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GeNePi: a GPU-enhanced Next Generation Bioinformatics Pipeline for Whole Genome Sequencing Analysis

Next Generation Sequencing (NGS) has revolutionized genome biology, enabling the rapid sequencing of an entire human genome and facilitating the integration of Whole Genome Sequencing (WGS) into both research and clinical applications. The high-throughput nature of NGS and the complex data processing required has driven the need for advanced computational infrastructures to analyse these large datasets. The aim of this work is to introduce an innovative bioinformatic pipeline, named GeNePi, for the efficient and precise analysis of WGS short paired-end reads. Built on the Nextflow framework with a modular structure, GeNePi incorporates GPU-accelerated algorithms and supports multiple work-flow configurations. The pipeline automates the extraction of biologically relevant insights from raw WGS data, including: disease-related variants such as single nucleotide variants (SNVs), small insertions or deletions (INDELs), copy number variants (CNVs), and structural variants (SVs). Optimized for high-performance computing (HPC) environments, it takes advantage of job-scheduler submissions, parallelised processing, and tailored resource allocation for each analysis step. Tested on synthetic and real datasets, GeNePi accurately identifies genomic variants, with performances comparable to that of state-of-art tools. These features make GeNePi a valuable instrument for large-scale analyses in both research and clinical contexts, representing a key step towards the establishment of National Centers for Computational and Technological Medicine.

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Optimizing Metagenome Analysis for Early Detection of Colorectal Cancer: Benchmarking Bioinformatics Approaches and Advancing Cross-Cohort Prediction

Colorectal cancer (CRC) continues to be a major global public health challenge. Extensive research has underscored the critical role of the gut microbiome for diagnostics of CRC. However, early-stage prediction of CRC, particularly at the precancerous adenomas (ADA) stage, remains challenging due to the instability of microbial features across cohorts. In this study, we conducted a systematic analysis of 2,053 gut metagenomes from 14 globally-sampled public cohorts and a newly recruited cohort. Despite substantial regional and cohort-level heterogeneity in microbiome composition, we elucidated that the consistent dynamic patterns of microbial signatures are the fundamental for CRC detection. These patterns enabled robust performance in both inter-cohort and independent validations using an optimized bioinformatics framework. In contrast, such basis was lacking in ADA-associated microbial markers, limiting the generalizability of early detection models. To address this, we developed an instance-based transfer learning approach, Meta-iTL, which effectively leveraged knowledge from existing datasets to detect CRC risk at the ADA stage in the newly recruited cohort. Thus, Meta-iTL overcomes challenges posed by cohort-specific variability and limited data availability, advances the application of non-invasive approaches for the early screening and prevention of CRC.

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Bioinformatic analysis of the variability of Tax1 and Tax2 proteins of the human T-cell lymphotropic virus (HTLV)

MotivationThe pathological differentiation in humans between HTLV-1 and HTLV-2 viruses is due, among other parameters, to the variability in a viral protein, Tax (Tax1 and Tax2 respectively), with the second virus being a candidate to interfere with HIV-1 infection, which has allowed us to assess the importance of further investigating Tax. ResultsBoth the degree of conservation and the genomic and protein variability between Tax1 and Tax2 have been expressed in this work through bioinformatics tools. The knowledge about Tax2 related to the interfering capacity on HIV-1 compared to the absence of such a function in Tax1 is corroborated with our analyses, highlighting certain variations between both sequences that could explain the functional differences in pathogenicity that we show in this work. Contactroberto117343@gmail.com; hwfcojavier32@gmail.com; hwfcojavier32@hotmail.com

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Integrative Machine Learning and Bioinformatics Analysis to Identify Cellular Senescence-Related Genes and Potential Therapeutic Targets in Ulcerative Colitis and Colorectal Cancer

BackgroundUlcerative colitis (UC) is a chronic inflammatory condition that predisposes patients to colorectal cancer (CRC) through mechanisms that remain largely undefined. Given the pivotal role of cellular senescence in both chronic inflammation and tumorigenesis, we integrated machine learning and bioinformatics approaches to identify senescence{square}related biomarkers and potential therapeutic targets involved in the progression from UC to CRC. MethodsGene expression profiles from six GEO datasets were analyzed to identify differentially expressed genes (DEGs) using the limma package in R. Weighted gene co expression network analysis (WGCNA) was employed to delineate modules significantly associated with UC and CRC, and the intersection of DEGs, key module genes, and senescence related genes from the CellAge database yielded 112 candidate genes. An integrated machine learning (IML) model, utilizing 12 algorithms with 10 fold cross validation was constructed to pinpoint key diagnostic biomarkers. The diagnostic performance of the candidate genes was evaluated using receiver operating characteristic (ROC) analyses in both training and validation cohorts. In addition, immune cell infiltration, protein protein interaction (PPI) networks, and drug enrichment analyses, including molecular docking were performed to further elucidate the biological functions and therapeutic potentials of the identified genes. ResultsOur analysis revealed significant transcriptomic alterations in UC and CRC tissues, with the turquoise module demonstrating the strongest association with disease traits. The IML approach identified five pivotal genes (ABCB1, CXCL1, TACC3, TGFBI, and VDR) that individually exhibited AUC values >0.7, while their combined diagnostic model achieved an AUC of 0.989. Immune infiltration analyses uncovered distinct immune profiles correlating with these biomarkers, and the PPI network confirmed robust interactions among them. Furthermore, drug enrichment and molecular docking studies identified several promising therapeutic candidates targeting these senescence{square}related genes. ConclusionsThis study provides novel insights into the molecular interplay between cellular senescence and the UC to CRC transition. The identified biomarkers not only offer strong diagnostic potential but also represent promising targets for therapeutic intervention, paving the way for improved clinical management of UC associated CRC.

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A Bioinformatic Investigation into the Role of ITGB1 in Cancer Prognosis and Therapeutic Resistance

Integrin {beta} 1 is a crucial transmembrane protein that regulates cellular adhesion, migration, and signal transduction, processes essential for cancer progression. This study investigates the role of ITGB1, the gene that encodes Integrin {beta}1, in various cancers using bioinformatics tools. By analyzing gene expression data across different cancer types and normal tissues, the study identifies significant upregulation of ITGB1 in 12 cancer types. We find elevated expression of ITGB1 is associated with poor prognosis in multiple tumors, suggesting its potential as a biomarker for cancer progression and therapeutic resistance. Further analysis reveals ITGB1s correlation with chemoresistance and immunoresistance genes, highlighting its involvement in cancer treatment evasion. The study also explores the expression and role of genes that are highly related to ITGB1 in tumor and patient prognosis, offering insights into potential molecular pathways and therapeutic targets. These findings underscore the clinical relevance of ITGB1 in cancer prognosis and therapy.

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Antibody-Based Targeting of the SPP1-CD44 Axis in Pediatric High-Grade Glioma through Single-Cell and Structural Bioinformatics

Pediatric high-grade glioma (pHGG) is a highly aggressive brain tumor characterized by transcriptional plasticity and an immunosuppressive microenvironment. Single-cell RNA-seq analysis revealed diverse malignant and immune cell populations, with tumor-associated macrophages (TAMs) emerging as the primary source of SPP1 (osteopontin), a glycoprotein that suppresses T cell activation through CD44 binding. Cell-cell communication analysis identified the SPP1-CD44 axis as a dominant immunosuppressive pathway in the tumor microenvironment. Despite extensive transcription factor screening, no strong regulators of SPP1 were identified, suggesting regulation occurs via alternative mechanisms. To assess structural features of SPP1, replica exchange molecular dynamics simulations were performed, revealing that the CD44-binding domain is conformationally stable. Phosphorylation at Ser169, a conserved site, further stabilized this region, suggesting a potential mechanism for enhanced CD44 interaction. To disrupt this axis, among 2,500 variants of anti-SPP1 23C3 antibody, a lead candidate variant (23C3-v1) with improved SPP1 binding affinity and minimal sequence divergence was identified. Furthermore, humanized 23C3-v1 (Hu23C3-v1) was designed to neutralize Class I and Class II epitope hits from murine antibody derived 23C3-v1 antibody. Together, this study integrates transcriptomic and structural bioinformatics approaches to the target SPP1-CD44 axis, which can help reduce immunosuppressive characteristics of pHGG tumor microenvironment (TME).

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A novel bioinformatics approach reveals key transcription factors regulating type 1 diabetes-associated transcriptomes

We developed a novel bioinformatics pipeline that reveals key transcription factors (TFs) regulating type 1 diabetes transcriptomes by combining automated Python workflows, DESeq2-based differential expression analysis, motif enrichment, and genome-wide TF abundance profiling, a rare but powerful strategy that deepens our understanding of disease mechanisms. This approach not only uncovers TFs driving pathology but also quantifies TF abundance across multiple genomic loci, enabling rapid and precise monitoring of their occupancy. Analyzing 21 RNA sequencing datasets, including 13 from early-stage T1D patients and 8 matched controls, we identified nearly 6 000 differentially expressed genes; 1 900 met strict significance and fold-change criteria and 211 are previously uncharacterized transcripts that distinguish T1D from healthy samples. Pathway analysis highlighted disruptions in beta-cell signaling, ALK-linked drug responses, neurodegenerative processes, and cytoskeletal organization. Upstream motif analysis revealed enrichment of Myc/Max, AP-1, SP-1, TATA-box, and NF-{kappa}B binding sites in upregulated genes, confirming their central role in the T1D transcriptome. By placing TFs at the core of our discovery platform, this work uncovers novel molecular drivers of T1D and identifies actionable biomarkers and therapeutic targets for personalized treatment.

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Bioinformatic Mining of Novel Lipopeptides Enabled by Daptomycin Cs Domain and Structural Modeling

Amidst the escalating crisis of antibiotic resistance, lipopeptides have emerged as promising therapeutic candidates due to their unique amphipathic structures. In this study, we developed a systematic bioinformatic platform using the condensation starter (Cs) domain of daptomycin as a molecular probe. Sequence similarity network (SSN) analysis identified 613 potential lipopeptide biosynthetic gene clusters (BGCs), with 432 (70.5%) originating from Streptomyces species. Subsequent integration of antiSMASH boundary prediction and evolutionary analysis prioritized 33 candidate BGCs harboring multiple post-modification modules. Five novel BGC types were ultimately selected based on Cs domain homology (<40% identity) and modification complexity. AlphaFold3 modeling revealed that WP_386473946.1 possess distinctive loop architecture, an expanded catalytic cavity, and a unique Asp60-Ala90 structural unit. Crucially, glycine residues adjacent to the conserved HHxxDG motif in the active pocket provide key targets for substrate recognition and rational engineering. This work delivers structure-guided genomic resources and molecular blueprints for accelerated discovery of antidrug-resistant lipopeptides.

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EVscope: A Comprehensive Bioinformatics Pipeline for Accurate and Robust Analysis of Total RNA Sequencing from Extracellular Vesicles

MotivationExtracellular vesicle (EV) RNA sequencing has emerged as a powerful approach for studying RNA biomarkers and intercellular communication. Nevertheless, the extremely low abundance, fragmented nature and ubiquitous tissue origin of EV RNAs, alongside potential contamination from co-isolated materials, such as free DNA and bacterial RNA, pose substantial analytical challenges. These complexities highlight a pressing need for a standardized, computational workflow that ensures robust quality control and EV RNA characterization. ResultsHere, we present EVscope, an open-source bioinformatics pipeline designed specifically for processing EV RNA-seq datasets. EVscope employs an optimized genome-wide expectation-maximization (EM) algorithm that significantly improves multi-mapping read assignment at single-base resolution by effectively leveraging alignment scores (AS) and local read coverage, specifically tailored for fragmented and low-abundance EV RNAs. Notably, EVscope uniquely generates EM-based BigWig files for downstream analysis, a capability currently unavailable in existing EM-based BigWig quantification tools. The pipeline systematically integrates 27 major steps, including quality control, analysis of library structure, contamination assessment, read alignment, read strandedness detection, UMI-based deduplication, RNA quantification, genomic DNA (gDNA) contamination correction, cellular and tissue source inference and visualization with a comprehensive HTML report. EVscope incorporates a comprehensive, updated annotation covering 19 distinct RNA biotypes, encompassing protein-coding genes, lncRNAs, miRNAs, piRNAs, retrotransposons (LINEs, SINEs, ERVs), and additional non-coding RNAs (tRNAs, rRNAs, snoRNAs). Furthermore, it leverages two highly balanced circRNA detection algorithms for robust circular RNA identification. Notably, a downstream module enables the inference of the tissue/cellular origins of EV RNAs using bulk and single-cell RNA-seq reference datasets. EVscope is implemented as a convenient, single-command Bash pipeline leveraging Conda-managed standard software packages and custom scripts, ensuring reproducibility and straightforward deployment. Availability and implementationCode, documentation, and tutorials are available at GitHub (https://github.com/TheDongLab/EVscope) and archived on Zenodo (https://zenodo.org/records/15577789).

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CRESSENT: a Bioinformatic Toolkit to Explore and Improve ssDNA Virus Annotation

Single-stranded DNA (ssDNA) viruses are important components of diverse ecosystems, however, it remains challenging to systematically identify and classify them. This is in part due to their broad host range and resulting genomic diversity, structure, and rapid evolution rates. In addition, distinguishing genuine ssDNA genomes from contaminating sequences in metagenomic datasets (e.g., from commercial kits) has been an unresolved issue for years. Here, we present CRESSENT (CRESS-DNA Extended aNnotation Toolkit), a comprehensive and modular bioinformatic pipeline focused on ssDNA virus genome-to-analysis and annotation. The pipeline integrates multiple functionalities organized into six modules: sequence dereplication, decontamination, phylogenetic analysis, motif discovery, stem-loop structure prediction, and recombination detection. Each module can be used independently or in combination with others, allowing researchers to customize their analysis workflow. With this tool, researchers can comprehensively and systematically include ssDNA viruses in their viromics workflows and facilitate comparative genomic studies, which are often limited to dsDNA viruses, therefore leaving behind a crucial component of the microbiome community under study.

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BioinAI: a general bioinformatic framework for multi-level transcriptomic data analysis using multiple semi-agents

Clinical and biological insights from large-scale transcriptomic data are often limited by technical variability and analytical complexity. Here, we introduce BioinAI, a general bioinformatic framework designed for multi-level transcriptomic data analysis. As part of the BioinAI framework, two algorithms named DeepAdvancer and stNiche were developed to improve data integration and analytical efficiency. DeepAdvancer leverages a class-aware adversarial autoencoder to reconstruct gene-expression profiles from 49,738 samples across 131 skin conditions. These profiles revealed a conserved inflammatory axis and a transcriptomic continuum which link diverse diseases through shared immune responses and structural programs. stNiche leverages spatial graph networks and symmetry-aware matching to identify functional cellular niches and reveals microstructural alterations across development, homeostasis, and disease. For instance, it identified a fibroblast-immune niche surrounding hair follicles in healthy skin, which disappears in pathological states. In addition, BioinAI provides a user-friendly online analysis platform powered by multiple semi-agents (www.bioinai.com), significantly facilitating the extraction of biological insights to advance scientific research.

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A systematic benchmark of bioinformatics methods for single-cell and spatial RNA-seq Nanopore long-read data

Alternative splicing plays a crucial role in transcriptomic complexity, yet remains difficult to resolve at the single-cell level due to the limitations of short-read technologies. Coupling single-cell with long-read sequencing offers full-length transcript coverage, enabling more accurate isoform detection. Multiple specialized computational tools tailored for single-cell and spatial long-read transcriptomics have been developed, with diverse strategies. To compare the effectiveness of these approaches, we generated paired short-read and Nanopore long-read single-cell datasets, tailored for benchmarking bioinformatics tools. We evaluated ten state-of-the-art methods, spanning four analytical dimensions: barcodes and UMI detection, demultiplexing and UMI clustering, gene-level expression profiling, and isoform detection and quantification. Using real and simulated datasets across different protocols, sequencing depths and chemistries, we assessed the accuracy, robustness, and scalability of each tool. Our results revealed method-specific trade-offs, and highlight the importance of sequencing quality and UMI correction strategies. This benchmark provides a practical resource for optimizing isoform analysis and accurate gene expression profiling in single-cell and spatial transcriptomics using long-read sequencing. Our benchmarking workflow is designed to be reusable, thereby enabling method developers to compare their own approaches against the set of reference methods evaluated in this work.

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Discovery of Prognostic Biomarkers in Gastric Cancer Through Machine Learning and Bioinformatics Analysis of Gene Expression Data

Gastric cancer (GC) often gets diagnosed in its advanced stages, resulting in poorer prognoses. To identify potential biomarkers in GC, we used fifteen datasets from NCBI-GEO and integrated them into a complete dataset. From the complete dataset, we extracted a subset of only the known cancer driver genes. Using Recursive Feature Elimination (RFE), mutual information (MI), and tree-based (TB) method (SelectFromModel), we extracted top gene features using RFE (10, 20, 30, 40, and 50) and 50 features each from MI and TB method. Subsequently, we applied machine learning classifiers to these selected gene features to classify cancer and normal samples. The SVC classifiers demonstrated better performance when utilizing the top 50 gene features using RFE and MI, while the AB classifier achieved the highest performance using TB for the complete dataset and for driver datasets, RF performed well using 40 features using RFE and SVC, and ET showed up better performance using 50 features using MI and TB feature selection for the test dataset. After combining all the genes from both datasets from and from all three feature selection methods, only 115 showed differentially expressed genes. A Lasso-penalized Cox regression model was applied to narrow down the gene selection to fourteen. This study highlights the effectiveness of integrating machine learning and bioinformatics analysis to identify new biomarkers for GC.

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Evolutionary and Structural Bioinformatics Reveal GPR89 as a Conserved Solute Carrier Transporter

Also called the Golgi pH regulator (GPHR), GPR89 is an orphan membrane protein found in nearly all eukaryotic lineages. Despite its broad phylogenetic distribution, the evolutionary history, structural diversity, and function of GPR89 remain poorly understood. In this study, we present a comprehensive bioinformatic analysis of GPR89 in Eukarya by integrating phylogenetic reconstruction, genomic synteny, sequence conservation, and structural modeling. While GPR89 is typically encoded as a single-copy gene, we identified lineage-specific duplications in both vascular plants and vertebrates. In contrast to the large sequence conservation, large differences can be observed in whether plants and animals preserve the gene structure flanking GPR89. Structural phylogenetic clustering places GPR89 within the solute carrier (SLC) superfamily, supporting previous reports claiming transporter-like activity rather than GPCR signaling. Predicted structures reveal a unique intracellular hairpin loop and a conserved transmembrane core compatible with transport activity. Our findings provide a unifying framework for interpreting the divergent functional roles reported for GPR89 and establish it as a structurally conserved, evolutionarily stable member of the SLC superfamily.

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ChatMDV: Democratising Bioinformatics Analysis Using Large Language Models

BackgroundThe rapid advancement in single-cell, spatial omics, imaging, and genomic technologies requires robust analytical and visualisation platforms capable of managing complex biological data. Tools such as Multi-Dimensional Viewer (MDV) offer comprehensive interfaces for data exploration, but still require manual configuration and computational expertise to generate visualisation outputs, limiting accessibility for many users. ResultsWe present ChatMDV, a natural language interface integrated with MDV that allows users to generate high-quality interactive visualisations through natural language commands. ChatMDV employs a retrieval-augmented generation (RAG) pipeline combined with large language models (LLMs) to translate user queries into reproducible Python code and interactive output. This approach enables exploratory and targeted analysis in diverse biological domains. We demonstrate ChatMDVs capabilities using three datasets of increasing complexity: the Peripheral Blood Mononuclear Cells 3K (PBMC3K) dataset, the lung cancer atlas dataset hosted at the Human Cell Atlas and the longitudinal TAURUS study single-cell RNA-sequencing (scRNA-seq) dataset. ConclusionsBy bridging the gap between natural language processing and bioinformatics visualisation, ChatMDV reduces technical barriers, enhances reproducibility, and supports more inclusive scientific inquiry. Its modular design and adherence to FAIR (Findability, Accessibility, Interoperability, and Reuse) principles make it a scalable and adaptable framework for accelerating biological data analysis. Key PointsO_LIChatMDV enables users to create interactive visualisations from biological datasets using natural language. C_LIO_LIThe system combines large language models with MDVs graphical platform to simplify data exploration. C_LIO_LIIt supports reproducibility, adaptability, and FAIR data practices, making it suitable for a wide range of users and use cases. C_LI

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