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Prognostic impact of the lipid metabolism gene AGPAT4 in the tumor immune microenvironment of thyroid cancer. 脂质代谢基因AGPAT4在甲状腺癌肿瘤免疫微环境中的预后影响
Genomics & informatics Pub Date : 2026-01-10 DOI: 10.1186/s44342-025-00065-0
Ying Zhu, Wenbo Xu, Xuejing Bai, Yanyuan Qiao, Dan Ye
{"title":"Prognostic impact of the lipid metabolism gene AGPAT4 in the tumor immune microenvironment of thyroid cancer.","authors":"Ying Zhu, Wenbo Xu, Xuejing Bai, Yanyuan Qiao, Dan Ye","doi":"10.1186/s44342-025-00065-0","DOIUrl":"10.1186/s44342-025-00065-0","url":null,"abstract":"<p><strong>Background: </strong>Thyroid cancer (THCA) is a common malignant tumor of the endocrine system, and significant clinical challenges remain in its diagnosis and prognostic evaluation. This study aims to elucidate the role of AGPAT4 in thyroid cancer by investigating its expression, involvement in metabolic pathways, and potential as a prognostic biomarker.</p><p><strong>Methods: </strong>We analyzed data from 512 thyroid cancer patients and 279 controls, performed differential expression analysis of AGPAT4 in thyroid cancer, analyzed the gene expression correlation of AGPAT4 in thyroid cancer, and the protein-protein interaction (PPI) network and functional enrichment analysis of AGPAT4 and its differentially expressed genes (DEGs) were constructed. The Kruskal-Wallis test and receiver operating characteristic (ROC) curve analysis were used to investigate the correlation between AGPAT4 expression and clinicopathological characteristics as well as its diagnostic efficacy. Cox regression analysis and Kaplan-Meier analysis were employed to evaluate its prognostic value. Additionally, single-sample gene set enrichment analysis (ssGSEA) was utilized to explore the association between AGPAT4 expression and the level of immune infiltration in the tumor microenvironment.</p><p><strong>Results: </strong>Our findings revealed that AGPAT4 was significantly downregulated in thyroid cancer (THCA) tissues (P < 0.001), suggesting a potential tumor-suppressive role of AGPAT4 in thyroid cancer. AGPAT4 exhibited robust efficacy in distinguishing tumor tissues from normal tissues, with an area under the receiver operating characteristic curve (AUC) of 0.973. Furthermore, AGPAT4 expression levels were significantly correlated with pathological stage and survival rate (P < 0.05). Kaplan-Meier survival analysis showed that patients with high AGPAT4 expression had better progression-free interval (PFI) (HR = 0.45, P = 0.007). Protein-protein interaction (PPI) network and functional enrichment analyses revealed that AGPAT4 is involved in key pathways associated with thyroid cancer progression. Immune infiltration analysis suggested an association between AGPAT4 expression and immune responses in the tumor microenvironment.</p><p><strong>Conclusion: </strong>AGPAT4 holds promise as a potential biomarker for the differential diagnosis and prognostic assessment of thyroid cancer, thereby providing a possible reference for the further exploration of therapeutic strategies against this disease.</p>","PeriodicalId":94288,"journal":{"name":"Genomics & informatics","volume":" ","pages":"1"},"PeriodicalIF":0.0,"publicationDate":"2026-01-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12879322/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145947068","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Peptide‑based therapeutics targeting the SLC39A14‑PIWIL2 fusion in hepatocellular carcinoma. 靶向SLC39A14 - PIWIL2融合治疗肝细胞癌的肽基疗法
Genomics & informatics Pub Date : 2025-12-20 DOI: 10.1186/s44342-025-00060-5
Masaud Shah, Sung Ung Moon, Ji-Hye Choi, Min Jae Kim, Hyun Goo Woo
{"title":"Peptide‑based therapeutics targeting the SLC39A14‑PIWIL2 fusion in hepatocellular carcinoma.","authors":"Masaud Shah, Sung Ung Moon, Ji-Hye Choi, Min Jae Kim, Hyun Goo Woo","doi":"10.1186/s44342-025-00060-5","DOIUrl":"10.1186/s44342-025-00060-5","url":null,"abstract":"<p><p>Fusion genes are key oncogenic drivers in various cancers; however, their role in hepatocellular carcinoma (HCC) remains underexplored. Here, we analyzed RNA-seq data from 68 HCC patients and identified several fusion products where SLC39A14-PIWIL2 stood out a putative driver. Functional assays revealed that the promoter of SLC39A14 potentially drives the overexpression of a truncated PIWIL2 protein (tPIWIL2), which retains its oncogenic MID and PIWI domains, in liver tissues. Both the wild-type and tPIWIL2 were found to interact with oncogenic partners HDAC3 and NME2 through these domains, as demonstrated by structural modeling and molecular dynamics simulations. To disrupt these interactions, we designed novel decoy peptides that potentially competes with both HDAC3 and NME2, effectively inhibiting PIWIL2-driven tumor activity in Huh7, HepG2, SNU449, and SNU398 HCC cell lines. Among the tested candidates, NEP1 markedly suppressed PIWIL2-driven oncogenic activity, and its co-administration with 5-fluorouracil (5-FU) significantly reduced PIWIL2-induced chemoresistance, thereby enhancing therapeutic efficacy. Collectively, these findings establish SLC39A14-PIWIL2 as a novel oncogenic fusion in HCC and highlight fusion protein-targeted peptide therapeutics as a promising avenue for precision treatment in HCC.</p>","PeriodicalId":94288,"journal":{"name":"Genomics & informatics","volume":" ","pages":"28"},"PeriodicalIF":0.0,"publicationDate":"2025-12-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12720462/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145800957","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Metagenomic analysis of microbiome spatial dynamics in urban river confluence affected by city wastewater. 城市污水影响下城市河流汇合处微生物群空间动态的宏基因组分析
Genomics & informatics Pub Date : 2025-12-04 DOI: 10.1186/s44342-025-00054-3
Nahid Parwin, Sangita Dixit, Sriansh Das, Rajesh Kumar Sahoo, Enketeswara Subudhi
{"title":"Metagenomic analysis of microbiome spatial dynamics in urban river confluence affected by city wastewater.","authors":"Nahid Parwin, Sangita Dixit, Sriansh Das, Rajesh Kumar Sahoo, Enketeswara Subudhi","doi":"10.1186/s44342-025-00054-3","DOIUrl":"10.1186/s44342-025-00054-3","url":null,"abstract":"&lt;p&gt;&lt;strong&gt;Background: &lt;/strong&gt;Environmental pollutants have a profound impact on microbial dynamics. This study highlights the influence of anthropogenic activity on the shift in bacterial diversity in the catchment area compared to upstream and downstream at Kathajodi, using a metagenomic approach for the first time in River Kathajodi.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Methods: &lt;/strong&gt;Water samples were collected from upstream, catchment, and downstream locations and transported at 4°C to the laboratory for DNA extraction, library preparation, sequencing, and physicochemical analysis employing inductively coupled plasma. The extracted DNA was sequenced via the Illumina HiSeq platform and analyzed through MG-RAST for taxonomic and functional classification using KEGG and COG annotations. Statistical diversity analysis, including rarefaction curves, alpha- and beta-diversity indices, and Venn diagrams, provided insights into microbial composition and community variations across sites.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Results: &lt;/strong&gt;A significant abundance of pollution indicator members of phylum Bacteroidetes (29.82%) in the catchment (CM), highly contaminated with metals, fecal, and other organic pollutants, could be attributed to their high metabolic capabilities to degrade them. The pristine upstream (US) exhibited an abundance of Shewanella (25.04%), Pseudomonas (17.35%), and Synechococcus (5.62%). The CM, influenced by high anthropogenic activity, showed higher abundances of Flavobacterium (5.20%), Arcobacter (4.05%), and Bacteroides (3.88%). In contrast, downstream (DS), with fewer anthropogenic activities, displayed higher abundances of Aeromonas (4.40%), Acidovorax (0.52%), and Acidimicrobium (0.32%). The highest bacterial diversity of CM could be due to the influence of the physicochemical properties of city waste effluent. From the Venn diagram, 73 common OTUs at the genera level were observed in all three sites, which indicates that the native microflora of the river water niche remains unaffected irrespective of the temporary changes in the vicinity. The functional profiling through KEGG and COG revealed that CM was enriched in carbohydrate metabolism (12.11%), while DS exhibited higher contributions to amino acid metabolism, along with the highest relative abundance of general function prediction (R) (12.89%), all indicative of stress adaptation and metabolic flexibility under polluted conditions. The clean upstream is home to oxygen-loving helpful bacteria, the catchment supports nutrient-hungry and sewage-linked microbes, while the downstream is dominated by metal-tolerant and possibly harmful bacteria, showing the clear impact of human activities along the river.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Conclusions: &lt;/strong&gt;The marked shift in bacterial diversity between US, CM, and DS regions highlights the ecological consequences of anthropogenic impact. These findings emphasize the need for effective environmental management to safeguard water quality and prevent undesirable health iss","PeriodicalId":94288,"journal":{"name":"Genomics & informatics","volume":" ","pages":"27"},"PeriodicalIF":0.0,"publicationDate":"2025-12-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12676890/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145673322","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Towards a transparent and reproducible AI-assisted research paper writing. 朝着透明和可重复的人工智能辅助研究论文写作的方向发展。
Genomics & informatics Pub Date : 2025-12-02 DOI: 10.1186/s44342-025-00057-0
Jeongbin Park
{"title":"Towards a transparent and reproducible AI-assisted research paper writing.","authors":"Jeongbin Park","doi":"10.1186/s44342-025-00057-0","DOIUrl":"10.1186/s44342-025-00057-0","url":null,"abstract":"<p><p>Artificial intelligence (AI)-assisted scientific writing is now a common practice in academic publishing, yet concerns persist regarding the authenticity and reproducibility of AI-generated content. While AI tools offer significant advantages, particularly for non-native English speakers who face substantial linguistic barriers in scientific communication, the risk of AI hallucinations and fabricated citations threatens the integrity of scholarly discourse. Journals often require disclosure of the entire AI prompt rather than meaningful intellectual contributions, but this is becoming increasingly impractical as AI prompts are getting longer and more complex. In this paper, I argue that transparency in AI-assisted writing should focus on capturing the author's core research perspective and section-specific key points-the foundational elements that drive meaningful scientific communication. To address this challenge, I developed a web-based tool that implements a human-in-the-loop approach requiring authors to define their research perspective and create detailed outlines with key points before any AI text generation occurs. The tool mitigates AI hallucination by only allowing the use of user-provided citations and generating transparency reports documenting the key elements used for text generation. I validated this approach by writing this paper using the tool itself, demonstrating how the transparency reporting method works in practice. This methodology ensures that AI serves as a linguistic tool rather than a content generator, preserving scientific integrity while democratizing access to high-quality academic writing across linguistic and cultural boundaries.</p>","PeriodicalId":94288,"journal":{"name":"Genomics & informatics","volume":"23 1","pages":"26"},"PeriodicalIF":0.0,"publicationDate":"2025-12-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12670809/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145663141","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
SPICEiST: subcellular RNA pattern enhances cell clustering of imaging-based spatial transcriptomics. 亚细胞RNA模式增强了基于成像的空间转录组学的细胞聚类。
Genomics & informatics Pub Date : 2025-12-02 DOI: 10.1186/s44342-025-00056-1
Sungwoo Bae, Yuchang Seong, Dongjoo Lee, Hongyoon Choi
{"title":"SPICEiST: subcellular RNA pattern enhances cell clustering of imaging-based spatial transcriptomics.","authors":"Sungwoo Bae, Yuchang Seong, Dongjoo Lee, Hongyoon Choi","doi":"10.1186/s44342-025-00056-1","DOIUrl":"10.1186/s44342-025-00056-1","url":null,"abstract":"<p><strong>Background: </strong>Imaging-based spatial transcriptomics (ST) enables the quantification of gene expression at single-cell resolution while preserving spatial context, but its utility is limited by small gene panels and challenges in accurate cell segmentation. To address these limitations, we present a graph autoencoder framework that integrates subcellular transcript distribution patterns with cell-level gene expression profiles for enhanced cell clustering in imaging-based ST (SPICEiST).</p><p><strong>Results: </strong>The clustering performance of SPICEiST was systematically evaluated across several cancer datasets and gene panel sizes. The results demonstrate that SPICEiST consistently outperforms the conventional cell-level gene expression-based methods in distinguishing subtle differences in cell states, as measured by the number of cell clusters and clustering indices, such as the CHI and DBI. Moreover, the findings indicate that SPICEiST can further enhance the performance, even with advancements in cell segmentation, particularly for datasets with small gene panels. Overall, these improvements in cell clustering indices, CHI and DBI, were more pronounced in datasets with small gene panels of around 300 genes, in contrast to those with large panels containing over a thousand genes. Notably, SPICEiST also reveals more spatially intermixed and less compartmentalized cell clusters, a characteristic that better reflects the complex and heterogeneous nature of tumor microenvironments. This effect was especially evident in the datasets with large panels.</p><p><strong>Conclusions: </strong>These findings highlight the value of leveraging subcellular transcript patterns to overcome the inherent limitations of imaging-based ST, particularly for small gene panels, and may provide new insights into tumor heterogeneity.</p>","PeriodicalId":94288,"journal":{"name":"Genomics & informatics","volume":"23 1","pages":"23"},"PeriodicalIF":0.0,"publicationDate":"2025-12-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12670746/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145663187","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Metagenomic insights into microbial community alterations and co-occurrence networks in infective endocarditis. 感染性心内膜炎中微生物群落改变和共现网络的宏基因组学见解。
Genomics & informatics Pub Date : 2025-12-02 DOI: 10.1186/s44342-025-00059-y
Zahra Abedi, Mohammad Ali Sheikh Beig Goharrizi, Amirreza Abbasi, Negar Sadat Soleimani Zakeri, Helia Jangi
{"title":"Metagenomic insights into microbial community alterations and co-occurrence networks in infective endocarditis.","authors":"Zahra Abedi, Mohammad Ali Sheikh Beig Goharrizi, Amirreza Abbasi, Negar Sadat Soleimani Zakeri, Helia Jangi","doi":"10.1186/s44342-025-00059-y","DOIUrl":"10.1186/s44342-025-00059-y","url":null,"abstract":"<p><strong>Background: </strong>Infective endocarditis (IE) is a serious infection of the heart valves, and standard culture methods often miss the bacteria responsible, especially in culture-negative cases. To address this, we used 16S rRNA gene-based next-generation sequencing (NGS) on heart valve tissue. This approach allowed us to map out the bacterial communities present and evaluate their potential role in IE.</p><p><strong>Result: </strong>We identified six key bacterial genera-Enterococcus, Streptococcus, Coxiella, Staphylococcus, Haemophilus, and Cutibacterium-plus three specific species: Streptococcus troglodytae, Haemophilus parainfluenzae, and Coxiella burnetii. Our co-occurrence analysis showed that these bacteria tend to exist independently within infected valve tissue, with no significant correlations between them.</p><p><strong>Conclusion: </strong>We detected bacterial taxa, including Cutibacterium and Streptococcus troglodytae. Although S. troglodytae is rarely associated with IE, and Cutibacterium comprises low-abundance bacteria not typically linked to this condition. These findings demonstrate the value of NGS in identifying pathogens that standard culture methods may overlook. As these results are based on computational analyses, further laboratory validation is required. Incorporating NGS into diagnostic protocols may enhance pathogen detection in culture-negative IE and support more targeted treatment and prevention strategies.</p>","PeriodicalId":94288,"journal":{"name":"Genomics & informatics","volume":"23 1","pages":"25"},"PeriodicalIF":0.0,"publicationDate":"2025-12-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12670860/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145663011","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
A curation system of rice trait ontology with reliable interoperation by LLM and PubAnnotation. 基于LLM和PubAnnotation的水稻性状本体可靠互操作检索系统。
Genomics & informatics Pub Date : 2025-12-02 DOI: 10.1186/s44342-025-00058-z
Javeed Muhammad Ahmad, Yawen Liu, Jin-Dong Kim, Xinzhi Yao, Pierre Larmande, Jingbo Xia
{"title":"A curation system of rice trait ontology with reliable interoperation by LLM and PubAnnotation.","authors":"Javeed Muhammad Ahmad, Yawen Liu, Jin-Dong Kim, Xinzhi Yao, Pierre Larmande, Jingbo Xia","doi":"10.1186/s44342-025-00058-z","DOIUrl":"10.1186/s44342-025-00058-z","url":null,"abstract":"<p><strong>Background: </strong>Ontology frameworks are essential for organizing complex biological knowledge, such as genes, phenotypes, and pathways, and for ensuring consistent data annotation and retrieval. In biological research, ontologies like the Gene Ontology (GO) and crop-specific trait ontologies (TO) for Oryza sativa (rice) standardize terminology across studies, supporting cross-study comparison and hypothesis generation. However, ontology annotations usually rely on expert manual review of the literature, a process that is accurate but time-consuming, labor-intensive, and difficult to scale as biological data grows. Manual approaches are also prone to inconsistencies and errors. The emergence of large language models (LLMs) such as ChatGPT, DeepSeek, and KIMI, along with curated databases like Rice-Alterome and PubAnnotation, offers new opportunities for semi-automated ontology curation. This study explores how these technologies can be integrated to develop an efficient literature-based curation system for rice trait ontology.</p><p><strong>Methods: </strong>We developed a curation system that integrates Rice-Alterome-a comprehensive database of rice genomic variations, mutations, and sentence-level literature evidence linked to GO and TO terms with PubAnnotation, an open-source platform for collaborative text annotation. LLMs (DeepSeek and KIMI) were integrated via APIs to automate the extraction, annotation, and validation of trait-related information via prompt engineering. The system was evaluated through use cases designed to demonstrate its performance and functionality compared to manual curation.</p><p><strong>Results: </strong>The proposed system substantially enhanced the retrieval and organization of literature evidence compared to manual methods. The integrated platform, available through a dedicated website, connects Rice-Alterome, PubAnnotation, and LLMs to streamline ontology curation and evidence discovery. This framework reduces the time domain experts need to locate and validate relevant information and provides interactive tools for users to add, merge, or refine trait annotations. The LLM-driven prompt-based querying also improved the identification of implicit or missing information that may be overlooked during manual curation.</p><p><strong>Conclusions: </strong>Integrating LLMs with Rice-Alterome and PubAnnotation offers a promising solution for automating rice trait ontology curation. This approach accelerates evidence collection and enhances data consistency and accessibility. Future extensions of this framework will target additional crops such as wheat and maize and focus on refining LLM-based retrieval and annotation mechanisms for broader agricultural genomics applications.</p>","PeriodicalId":94288,"journal":{"name":"Genomics & informatics","volume":"23 1","pages":"24"},"PeriodicalIF":0.0,"publicationDate":"2025-12-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12670841/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145663013","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
From pixels to cell types: a comprehensive review of computational methods for spatial transcriptomics deconvolution. 从像素到细胞类型:空间转录组反褶积计算方法的全面回顾。
Genomics & informatics Pub Date : 2025-10-31 DOI: 10.1186/s44342-025-00055-2
Jahanzeb Saqib, Junil Kim
{"title":"From pixels to cell types: a comprehensive review of computational methods for spatial transcriptomics deconvolution.","authors":"Jahanzeb Saqib, Junil Kim","doi":"10.1186/s44342-025-00055-2","DOIUrl":"10.1186/s44342-025-00055-2","url":null,"abstract":"<p><p>Spatial transcriptomics technologies have significantly enhanced the analysis of gene expression profiles by retaining the spatial information of intact tissue sections and enabling the possibility of a more profound comprehension of tissue structures and cellular relationships. Despite this, most platforms have limited resolution, and at numerous capture spots, multiple signals from various cells are present, requiring deconvolution, a set of computational steps to deduce the underlying cellular composition. Over the last few years, a range of algorithms has been proposed to address this problem, each employing distinct computational principles and processing paradigms. The present review seeks to present a comprehensive analysis of twenty such algorithms, focusing on their methodological foundations. We contrast the underlying computational algorithms, modeling methods, and data processing pipelines that underlie them, and how they deal with external references, noise and sparsity in the data. By drawing out the conceptual as well as technical foundations of each algorithm, we aim to provide researchers a complete and hands-on grasp of the computational landscape of spatial transcriptomics deconvolution. This review is a methodological handbook to enable deep understanding of current deconvolution methods to develop novel strategies and help in selecting or applying these existing tools for different biological contexts.</p>","PeriodicalId":94288,"journal":{"name":"Genomics & informatics","volume":"23 1","pages":"22"},"PeriodicalIF":0.0,"publicationDate":"2025-10-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12577344/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145423791","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
In silico design of a multi-epitope pan vaccine targeting Schistosoma species. 以血吸虫为靶点的多表位泛疫苗的计算机设计。
Genomics & informatics Pub Date : 2025-10-27 DOI: 10.1186/s44342-025-00053-4
Daksh Gandvi, Charmi Jyotishi, Mansi Patel, Reeshu Gupta
{"title":"In silico design of a multi-epitope pan vaccine targeting Schistosoma species.","authors":"Daksh Gandvi, Charmi Jyotishi, Mansi Patel, Reeshu Gupta","doi":"10.1186/s44342-025-00053-4","DOIUrl":"10.1186/s44342-025-00053-4","url":null,"abstract":"<p><p>Schistosomiasis remains a significant public health burden, necessitating the development of effective vaccines against it. In this study, a multi-epitope subunit vaccine was designed against adenylate kinase 2 protein and evaluated for its potential to elicit protective immunity against three Schistosoma species. CTL, HTL, and B-cell epitopes were identified using immunoinformatics tools and linked using AAY and KK linkers, respectively. The 50S ribosomal protein L7/L12, a known TLR4 agonist, was incorporated as an adjuvant to enhance immune activation in the vaccine. Molecular docking and molecular dynamics (MD) simulations demonstrated a strong binding affinity between the vaccine and human TLR4, supported by low RMSD and Rg values, indicating structural stability. The negative binding energy further validated the vaccine's potential for engaging TLR4. The immunogenic profile predicted robust activation of CD4+ and CD8+ T cells, as well as neutralizing antibody responses. These findings highlight the potential of the vaccine to stimulate both cell-mediated and humoral immunity, making it a promising candidate for further experimental validation against schistosomiasis.</p>","PeriodicalId":94288,"journal":{"name":"Genomics & informatics","volume":"23 1","pages":"21"},"PeriodicalIF":0.0,"publicationDate":"2025-10-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12560484/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145380516","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Deciphering the linguistic blueprint of DNA: context-sensitive structures, statistical patterns, and regulatory implications. 解读DNA的语言蓝图:上下文敏感结构、统计模式和监管含义。
Genomics & informatics Pub Date : 2025-10-23 DOI: 10.1186/s44342-025-00052-5
Iskander Akhmetov, Timur Saparov, Volkan Duran, Alexander Pak
{"title":"Deciphering the linguistic blueprint of DNA: context-sensitive structures, statistical patterns, and regulatory implications.","authors":"Iskander Akhmetov, Timur Saparov, Volkan Duran, Alexander Pak","doi":"10.1186/s44342-025-00052-5","DOIUrl":"10.1186/s44342-025-00052-5","url":null,"abstract":"<p><p>DNA is often described as the \"language of life\" because it encodes biological information using nucleotide sequences. Unlike the traditional view focused on codon-to-amino acid mapping in coding regions, the vast non-coding genome reveals complex organizational patterns resembling natural language. This paper outlines essential approaches in DNA linguistics, including formal language theory, RNA secondary structure modeling, statistical methods, and phylogenetic analysis. Additionally, recent research on Indo-European populations shows correlations between lexical and phonemic traits and asymmetrical patterns of genetic inheritance. Together, these perspectives deepen our understanding of genome regulation, evolution, and the striking parallels between genetic and linguistic systems.</p>","PeriodicalId":94288,"journal":{"name":"Genomics & informatics","volume":"23 1","pages":"20"},"PeriodicalIF":0.0,"publicationDate":"2025-10-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12551216/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145357472","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
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