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10X Genomics
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10X Genomics
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10X Genomics
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10X Genomics
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10X Genomics
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10X Genomics
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Spatial Transcriptomics Inc
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10X Genomics
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Image Search Results
Journal: BMB Reports
Article Title: Recent advances in spatially resolved transcriptomics: challenges and opportunities
doi: 10.5483/BMBRep.2022.55.3.014
Figure Lengend Snippet: Integration of spatially resolved transcriptomic data with other methods
Article Snippet: Robust cell type decomposition (RCTD) is based on statistical model maximum-likelihood estimation to approximate the proportions of spatially localized cellular subtypes in spatially resolved transcriptomic data such as Slide-seq or
Techniques: Derivative Assay, In Situ Hybridization, Expressing, Microarray, Marker, Modification, Staining, In Silico, Hybridization, Sequencing, Imaging, Mass Spectrometry
Journal: Blood Science
Article Title: Spatially resolved transcriptomics: advances and applications
doi: 10.1097/BS9.0000000000000141
Figure Lengend Snippet: Major SRT methods.
Article Snippet: Sequencing-based methods such as Slide-seq and
Techniques: In Situ Hybridization, Amplification, Labeling, Imaging, Hybridization, Sequencing, Genome Wide, Tomography, High Throughput Screening Assay, Microscopy, Laser-Scanning Microscopy, Transgenic Assay, Staining, In Vivo, In Situ, Introduce
Journal: Blood Science
Article Title: Spatially resolved transcriptomics: advances and applications
doi: 10.1097/BS9.0000000000000141
Figure Lengend Snippet: Schematics of the main sequencing-based methods. (A) In tomo-seq, specimens are cryosectioned, and sections are collected in individual microtubes for spatially resolved transcriptomic analysis. (B) In LCM, an infrared laser melts the thermolabile polymer on a tissue section on a glass slide in the vicinity of the laser pulse, resulting in the removal of polymer-cell composite from the tissue. A UV laser can cut away cells of interest or ablate unwanted tissue, leaving cells of interest intact on the slide. (C) In NICHE-seq, tissue expressing a PA-GFP can be activated by 2-photon irradiation, allowing precise in situ labeling. Activated cells are sorted to perform MARS-seq. (D) In 10X Genomics’ Visium, tissue sections are placed on a barcoded glass slide containing 4 capture areas, each with around 5000 spatial spots. After HE staining and imaging, tissue permeabilization releases the mRNA and it is captured by spatial probes. LCM = laser-capture microdissection, PA-GFP = photoactivatable green fluorescent protein, MARS-seq =massively parallel scRNA-seq, UV=ultraviolet, HE staining = hematoxylin-eosin staining.
Article Snippet: Sequencing-based methods such as Slide-seq and
Techniques: Sequencing, Polymer, Expressing, Irradiation, In Situ, Labeling, Staining, Imaging, Laser Capture Microdissection
Journal: Cell reports
Article Title: Alveolar type I cells can give rise to KRAS-induced lung adenocarcinoma.
doi: 10.1016/j.celrep.2023.113286
Figure Lengend Snippet: Figure 3. Spatial transcriptomic profiling reveals distinct cell-origin-specific molecular and phenotypic presentation (A) H&E section generated as part of the Visium 10X spatial transcriptomic profiling performed on representative Gramd2:KRASG12D lung that contains multiple LUAD lesions. (B) High magnification views of distinct histologic regions within Gramd2:KRASG12D lung sections. (C) Spatial distribution of integrated clusters (ICs) across all six lung samples within the dataset. Colors indicate distinct ICs. Spatial transcriptomic sequencing was performed on three biological replicates from Sftpc:KRASG12D and Gramd2:KRASG12D mouse lungs. (D) Barplots of average number of array spots per section. Average (n = 3 samples) and error bars (percent standard deviation) are shown.
Article Snippet: Regions of Interest (ROIs) then underwent sample preparation including test slide sample sequencing using the
Techniques: Generated, Sequencing, Standard Deviation
Journal: Nature Communications
Article Title: Spatially resolved integrative analysis of transcriptomic and metabolomic changes in tissue injury studies
doi: 10.1038/s41467-025-68003-w
Figure Lengend Snippet: a Experimental workflow for spatial multi-omics profiling of rodent lung, consisting of agarose inflation of the lung tissue to facilitate the preservation of tissue integrity, followed by snap-freezing and cryo-sectioning to create consecutive sections, used for spatial transcriptomics and spatial metabolomics, respectively. b MAGPIE computational framework for co-registering same or consecutive section spatial transcriptomics (Visium) and metabolomics (mass spectrometry imaging, MSI) data. The pipeline’s inputs and outputs are in standardised Space Ranger-style and tabular formats to ensure compatibility with other tools. Preprocessing the MSI data produces a data-generated image used for landmark selection and subsequent image co-registration. The output from the pipeline is the MSI data with updated coordinates aligned to the Visium data. c To create a 1:1 mapping between Visium spots and MSI pixels, MAGPIE (by default) expands Visium spot radii, such that there are no gaps between spots, and then aggregates MSI pixels that fall within these spot boundaries. This results in matching observations between modalities and a processed object which can then be read by analysis toolkits, including semla . d Overview of downstream analysis options once the modalities are aligned into a matching coordinate system. Examples include joint clustering, dimensionality reduction, linking transcriptomic and metabolic changes to histologic information, and gene-peak correlation or multi-omics covariation network analysis. Spatial b.c. spatial barcode, CCF common coordinate framework. Source data are provided as a Source Data file.
Article Snippet: Consecutive sections from each lung were thaw-mounted on a
Techniques: Biomarker Discovery, Preserving, Mass Spectrometry, Imaging, Generated, Selection