visium datasets (Spatial Transcriptomics Inc)
Structured Review

Visium Datasets, supplied by Spatial Transcriptomics Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/visium datasets/product/Spatial Transcriptomics Inc
Average 90 stars, based on 1 article reviews
Images
1) Product Images from "Dissecting Sex‐Specific Pathology in K18‐hACE2 Transgenic Mice Infected With Different SARS‐CoV‐2 Variants"
Article Title: Dissecting Sex‐Specific Pathology in K18‐hACE2 Transgenic Mice Infected With Different SARS‐CoV‐2 Variants
Journal: Journal of Medical Virology
doi: 10.1002/jmv.70506
Figure Legend Snippet: Sex‐specific spatial transcriptomics analysis in Delta‐infected mouse lungs. Lungs from Delta‐infected female and male mice on 3‐ and 5‐days post infection (dpi) were processed for spatial transcriptomics. (A). H&E staining. (B) Spatial plots with dimensional reduction clustering overlay with individual clusters coded by color and each dot representing a capture spot. (C) Relative expression frequency of gene clusters across each sample in a bar plot. (D) Conserved gene markers in identified clusters shown in a dot plot with average gene expression denoted by a color (red = upregulated, blue = downregulated) and percent expression denoted by the size of a dot. (E) UMAP plots for individual samples with 6 identified major clusters. Each dot in the UMAP plots represents one of 1,317 ± 136 capture spots per sample shown in B and color denotes corresponding gene expression cluster.
Techniques Used: Infection, Staining, Expressing, Gene Expression
Figure Legend Snippet: Differential analysis of spatial transcriptomics identified gene markers within the lung immune cell clusters. Lungs from Delta‐infected female and male mice on 3‐ and 5‐days post infection (dpi) were analyzed by spatial transcriptomics. (A) Top 50 genes that are significantly associated with female (left) or male (right) ‘ImmuneCell’ cluster (presented in Figure ) in a dot plot with average gene expression denoted by a color (red = upregulated, blue = downregulated) and percent expression denoted by the size of a dot. (B) Gene expression of Gbp4, Psmb10, Saa3, or Fth1 in violin plot. (C) Spatially mapped gene expression of Gbp4, Psmb10, Saa3, or Fth1 on 3‐dpi. (D) Top 15 enriched pathways for female (left) and male (right) samples identified by gene ontology analysis.
Techniques Used: Infection, Gene Expression, Expressing


![Immunohistochemical quantification of PTPN7 in normal brain and gliomas. A TCGA proteomic analysis confirmed elevated PTPN7 expression in <t>glioblastoma</t> over normal tissue. B Summary table of PTPN7 density (mean ± SD) in normal tissue (n = 11) and IDH‐wildtype (n = 37) and IDH‐mutant glioma (n = 22). C Representative tissue cores (H&E, low‐power IHC, automated machine quantification, and high‐power IHC) reveal immunostaining ranging from 0.17 to 48.93. (Black = background [B], Blue = Tissue [T], Yellow “+” = staining cells). D , E Box plots of PTPN7 density by WHO grade for IDH‐wildtype or IDH‐mutant astrocytoma. F , G Comparisons of normal, low‐grade, and high‐grade groups. Elevated PTPN7 correlates with tumor grade in the IDH wildtype group but is obscure in the IDH mutant group](https://pub-med-central-images-cdn.bioz.com/pub_med_central_ids_ending_with_3406/pmc12103406/pmc12103406__12672_2025_2662_Fig5_HTML.jpg)
