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The rapid advancement of multi-omics single-cell technologies has significantly enhanced our ability to investigate complex biological systems at unprecedented resolution. However, many existing analysis tools are complex, requiring substantial coding expertize, which can be a barrier for computationally less competent researchers. To address this challenge, we present single-cell analyst, a user-friendly, web-based platform to facilitate comprehensive multi-omics analysis. Single-cell analyst supports a wide range of data types, including six single-cell omics: single-cell RNA sequencing (scRNA-sequencing), single-cell assay for transposase accessible chromatin sequencing (scATAC-seq sequencing), single-cell immune profiling (scImmune profiling), single-cell copy number variation, cytometry by time-of-flight, and flow cytometry and spatial transcriptomics, and enables researchers to perform integrated analyses without requiring programming skills. The platform offers both online and offline modes, providing flexibility for various use cases. It automates critical analysis steps, such as quality control, data processing, and phenotype-specific analyses, while also offering interactive, publication-ready visualizations. With over 20 interactive tools for intermediate analysis, single cell analyst simplifies workflows and significantly reduces the learning curve typically associated with similar platforms. This robust tool accommodates datasets of varying sizes, completing analyses within minutes to hours depending on the data volume, and ensures efficient use of computational resources. By democratizing the complex process of multi-omics analysis, single-cell analyst serves as an accessible, all-encompassing solution for researchers of diverse technical backgrounds. The platform is freely accessible at www.singlecellanalyst.org.
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http://dx.doi.org/10.1002/imt2.70038 | DOI Listing |
Analyst
September 2025
Department of Natural Product Biosynthesis, Max Planck Institute for Chemical Ecology, Jena 07745, Germany.
In this proof-of-concept work, we applied single-cell mass spectrometry to track the incorporation of an isotopically labelled precursor into plant specialized metabolites. The application of stable-isotope labelling to single cell systems could provide a unique window into the dynamics of synthesis and intercellular transport of structurally complex metabolites.
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August 2025
Institute of Advanced Clinical Medicine, Biomedical Engineering Department, International Cancer Institute, Peking University, Beijing 100083, China.
Mass cytometry, a cutting-edge single-cell analytical technique, has achieved high-resolution, high-throughput, and simultaneous detection of multiple parameters. This technique fundamentally differs from conventional flow cytometry by employing stable isotope (primarily lanthanide) tags instead of fluorophores, thereby overcoming spectral limitations. Among the diverse mass tag reagents developed to date, metal-chelated complexes using bifunctional chelators, particularly 1,4,7,10-tetraazacyclododecane-1,4,7,10-tetraacetic acid (DOTA) and diethylenetriaminepentaacetic acid (DTPA), have been widely used due to their exceptional thermodynamic stability, kinetic inertness under physiological conditions, and versatile conjugation chemistry.
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December 2025
Department of Cardio-Thoracic Surgery, Affiliated Jinhua Hospital, Zhejiang University School of Medicine, Jinhua, Zhejiang 321000, China.
Background: Idiopathic pulmonary fibrosis (IPF) is a fibrotic lung disease of unknown etiology with limited diagnostic and therapeutic options. DNA damage repair (DDR) plays an important role in the pathogenesis of lung diseases. The aim of this study was to identify core DDR genes involved in IFP progression and to assess their diagnostic potential and immunological relevance.
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June 2025
Department of General Surgery, The Fourth Affiliated Hospital China Medical University Shenyang Liaoning China.
Analyst
June 2025
School of Pharmacy, Nanjing Medical University, Nanjing, Jiangsu 211126, China.
A catalase-assisted peroxide quenching strategy is established by the injection of catalase, which consumes intracellular hydrogen peroxide generated from oxygen stress, into a living cell using a nanopipette. Accordingly, the amounts of reactive oxygen intermediates (ROIs) are quantified at the single cell level.
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