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This study evaluates the concordance between RNA sequencing (RNA-Seq) and NanoString technologies for gene expression analysis in non-human primates (NHPs) infected with Ebola virus (EBOV). A detailed comparison of both platforms revealed a strong correlation, with Spearman coefficients for 56 out of 62 samples ranging from 0.78 to 0.88. The mean and median coefficients were 0.83 and 0.85, respectively. Bland-Altman analysis confirmed high consistency across most measurements, with values falling within the 95% limits of agreement. Using a machine learning approach with the Supervised Magnitude-Altitude Scoring (SMAS) method trained on NanoString data, OAS1 was identified as a key gene signature for distinguishing RT-qPCR positive from negative samples. Remarkably, when used as the sole predictor in a logistic regression model, OAS1 maintained its predictive power on RNA-Seq data from the same cohort of EBOV-infected NHPs, achieving 100% accuracy in distinguishing infected from non-infected samples. OAS1 was also tested in a completely independent held-out test set, consisting of human monocyte-derived dendritic cells (DC) isolated and infected with different strains of the Ebola virus: wild-type (wt), VP35m, VP24m, along with a double mutant VP35m & VP24m, and again demonstrated a 100% accuracy rate in differentiating EBOV-infected from mock-infected samples, confirming its effectiveness as a predictive marker across diverse experimental setups and virus strains. Further differential expression analysis across both platforms identified 12 common genes (including ISG15, OAS1, IFI44, IFI27, IFIT2, IFIT3, IFI44L, MX1, MX2, OAS2, RSAD2, and OASL) that showed the highest levels of statistical significance and biological relevance. Gene Ontology (GO) analysis confirmed the involvement of these genes in key immune and viral infection pathways, highlighting their importance in EBOV infection. RNA-Seq uniquely identified genes such as CASP5, USP18, and DDX60, which are important in immune regulation and antiviral defense and were not detected by NanoString, demonstrating the broader detection capabilities of RNA-Seq. This study indicates a very strong agreement between RNA-Seq and NanoString platforms in gene expression analysis, with RNA-Seq displaying broader capabilities in identifying gene signatures.
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http://dx.doi.org/10.1186/s12864-025-11553-6 | DOI Listing |
NPJ Breast Cancer
August 2025
Cancer Early Detection Advanced Research Center, Knight Cancer Institute, Oregon Health & Science University, Portland, OR, USA.
Metastatic breast cancer remains largely incurable, and the mechanisms driving the transition from primary to metastatic breast cancer remain elusive. We analyzed the complex landscape of estrogen receptor (ER)-positive breast cancer primary and metastatic tumors using scRNA-seq data from twenty-three female patients with either primary or metastatic disease. By employing single-cell transcriptional profiling of unpaired patient samples, we sought to elucidate the genetic and molecular mechanisms underlying changes in the metastatic tumor ecosystem.
View Article and Find Full Text PDFLung Cancer
September 2025
Unit of Bioinformatics for Precision Oncology, Institut Català d'Oncologia, L'Hospitalet de Llobregat, Spain; Molecular Biology CORE. Center for Biomedical Diagnostics (CDB), Hospital Clínic de Barcelona. Translational Genomics and Targeted Therapies in Solid Tumors, August Pi i Sunyer Biomedical
Unlabelled: Pleural mesothelioma (PM) is a rare and lethal cancer with limited treatment options. Intratumor heterogeneity (ITH) has been postulated as one of the reasons for the poor treatment response observed in most PM patients. In this regard, we aimed to characterize ITH in a multi-site tumor specimen using single-cell RNA-sequencing (scRNA-seq).
View Article and Find Full Text PDFAndrology
July 2025
Centre for Reproductive Health, Hudson Institute of Medical Research, Clayton, Victoria, Australia.
Background: Testicular germ cell tumours (TGCTs) are amongst the most common malignancies in young men, and their incidence is increasing worldwide. Tissue heterogeneity hampers efforts to understand how TGCT precursors (termed germ cell neoplasia in situ; GCNIS) emerge and progress, restricting elucidation of new strategies for diagnosis and management.
Objectives: This study reports the use of spatial transcriptomic analysis in TGCT tissue sections.
Cell Genom
July 2025
Department of Biomedical Engineering, Oregon Health & Science University, Portland, OR, USA; Knight Cancer Institute, Oregon Health & Science University, Portland, OR, USA; Center for Biomedical Data Science, Oregon Health & Science University, Portland, OR, USA. Electronic address:
Cell deconvolution estimates cell type proportions from bulk omics data, enabling insights into tissue microenvironments and disease. However, practical applications are often hindered by batch effects between bulk data and referenced single-cell data, a challenge that is frequently overlooked. To address this discrepancy, we developed OmicsTweezer, a distribution-independent cell deconvolution model.
View Article and Find Full Text PDFFront Vet Sci
June 2025
Department of Veterinary Medicine, Institute of Veterinary Pathology, Freie Universität Berlin, Berlin, Germany.
Analyses of nucleic acids from archival tissues offer invaluable prospects for numerous fields of veterinary medicine, such as the study of differential gene expression in rare or historic diseases. The establishment of modern methodologies, however, raises questions regarding the comparability and reproducibility of data obtained from unlike tools. 3' RNA-Seq and direct RNA hybridization are such conceptually different approaches for high-throughput transcriptome analysis.
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