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denoist  (Spatial Transcriptomics Inc)

 
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    Spatial Transcriptomics Inc denoist
    a) Shown here is a region of the healthy lung sample assayed using Xenium, with the boundary expansion segmentation from 10x Xenium Ranger (Top) and Proseg (Bottom) segmentation. Each dot is a transcript molecule, molecules of lineage marker genes are coloured by their respective lineages. Black lines are segmentation boundaries. b) Log CPM (counts per million) normalised pseudobulked gene expression of 4 selected contaminating genes using 4 annotated immune cell types in the lung fibrosis Xenium data. Each data point is a sample and a lowess curve is fitted over all the samples. c) A high level schematic of the application of <t>DenoIST.</t>
    Denoist, supplied by Spatial Transcriptomics Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/denoist/product/Spatial Transcriptomics Inc
    Average 86 stars, based on 1 article reviews
    denoist - by Bioz Stars, 2026-05
    86/100 stars

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    1) Product Images from "Denoising image-based spatial transcriptomics data with DenoIST"

    Article Title: Denoising image-based spatial transcriptomics data with DenoIST

    Journal: bioRxiv

    doi: 10.1101/2025.11.13.688387

    a) Shown here is a region of the healthy lung sample assayed using Xenium, with the boundary expansion segmentation from 10x Xenium Ranger (Top) and Proseg (Bottom) segmentation. Each dot is a transcript molecule, molecules of lineage marker genes are coloured by their respective lineages. Black lines are segmentation boundaries. b) Log CPM (counts per million) normalised pseudobulked gene expression of 4 selected contaminating genes using 4 annotated immune cell types in the lung fibrosis Xenium data. Each data point is a sample and a lowess curve is fitted over all the samples. c) A high level schematic of the application of DenoIST.
    Figure Legend Snippet: a) Shown here is a region of the healthy lung sample assayed using Xenium, with the boundary expansion segmentation from 10x Xenium Ranger (Top) and Proseg (Bottom) segmentation. Each dot is a transcript molecule, molecules of lineage marker genes are coloured by their respective lineages. Black lines are segmentation boundaries. b) Log CPM (counts per million) normalised pseudobulked gene expression of 4 selected contaminating genes using 4 annotated immune cell types in the lung fibrosis Xenium data. Each data point is a sample and a lowess curve is fitted over all the samples. c) A high level schematic of the application of DenoIST.

    Techniques Used: Marker, Gene Expression

    Expression of ACTA2 from a zoomed-in section in Xenium human breast cancer dataset. Each dot is a segmented cell using 10x boundary expansion method, colour shows the log count of ACTA2 . Cells with 0 count are greyed out for visual clarity. b) Heatmap visualisation of gene expression of annotated cell types before (top) and after DenoIST (bottom). Columns are selected genes, annotated by the cell type they mark. Row are cell types. The log(mean count + 1) for each cell type is shown here. c) MECR before (top) and after (bottom) applying DenoIST to Xenium human breast cancer dataset. Rows and columns denote genes and each entry is the MECR of the corresponding pair. Note that genes that mark the same cell type are not expected to be mutually exclusive, but are shown here for positive control.
    Figure Legend Snippet: Expression of ACTA2 from a zoomed-in section in Xenium human breast cancer dataset. Each dot is a segmented cell using 10x boundary expansion method, colour shows the log count of ACTA2 . Cells with 0 count are greyed out for visual clarity. b) Heatmap visualisation of gene expression of annotated cell types before (top) and after DenoIST (bottom). Columns are selected genes, annotated by the cell type they mark. Row are cell types. The log(mean count + 1) for each cell type is shown here. c) MECR before (top) and after (bottom) applying DenoIST to Xenium human breast cancer dataset. Rows and columns denote genes and each entry is the MECR of the corresponding pair. Note that genes that mark the same cell type are not expected to be mutually exclusive, but are shown here for positive control.

    Techniques Used: Expressing, Gene Expression, Positive Control

    a) UMAP visualisation of lung fibrosis data after applying DenoIST. Sample TILD028MA is shown here. Cells with 0 count are greyed out for visual clarity. b) An airway section from fibrotic sample VUILD110. Each dot is a cell. Cells with 0 count are greyed out for visual clarity. Annotated airway cell types and gene expression (raw counts and DenoIST-adjusted counts) for KRT5 and MUC5B are shown. c) Proportions of RCTD classification using raw counts and DenoIST-adjusted counts in healthy sample VUHD116A. d) RCTD assignment weights of the second highest lineage of each cell in healthy sample VUHD116A, stratified by their manually annotated lineages. Cells with a pure identity should have low weights for the incorrect lineages.
    Figure Legend Snippet: a) UMAP visualisation of lung fibrosis data after applying DenoIST. Sample TILD028MA is shown here. Cells with 0 count are greyed out for visual clarity. b) An airway section from fibrotic sample VUILD110. Each dot is a cell. Cells with 0 count are greyed out for visual clarity. Annotated airway cell types and gene expression (raw counts and DenoIST-adjusted counts) for KRT5 and MUC5B are shown. c) Proportions of RCTD classification using raw counts and DenoIST-adjusted counts in healthy sample VUHD116A. d) RCTD assignment weights of the second highest lineage of each cell in healthy sample VUHD116A, stratified by their manually annotated lineages. Cells with a pure identity should have low weights for the incorrect lineages.

    Techniques Used: Gene Expression



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    denoist  (Spatial Transcriptomics Inc)
    86
    Spatial Transcriptomics Inc denoist
    a) Shown here is a region of the healthy lung sample assayed using Xenium, with the boundary expansion segmentation from 10x Xenium Ranger (Top) and Proseg (Bottom) segmentation. Each dot is a transcript molecule, molecules of lineage marker genes are coloured by their respective lineages. Black lines are segmentation boundaries. b) Log CPM (counts per million) normalised pseudobulked gene expression of 4 selected contaminating genes using 4 annotated immune cell types in the lung fibrosis Xenium data. Each data point is a sample and a lowess curve is fitted over all the samples. c) A high level schematic of the application of <t>DenoIST.</t>
    Denoist, supplied by Spatial Transcriptomics Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/denoist/product/Spatial Transcriptomics Inc
    Average 86 stars, based on 1 article reviews
    denoist - by Bioz Stars, 2026-05
    86/100 stars
    		  Buy from Supplier

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    a) Shown here is a region of the healthy lung sample assayed using Xenium, with the boundary expansion segmentation from 10x Xenium Ranger (Top) and Proseg (Bottom) segmentation. Each dot is a transcript molecule, molecules of lineage marker genes are coloured by their respective lineages. Black lines are segmentation boundaries. b) Log CPM (counts per million) normalised pseudobulked gene expression of 4 selected contaminating genes using 4 annotated immune cell types in the lung fibrosis Xenium data. Each data point is a sample and a lowess curve is fitted over all the samples. c) A high level schematic of the application of DenoIST.

    Journal: bioRxiv

    Article Title: Denoising image-based spatial transcriptomics data with DenoIST

    doi: 10.1101/2025.11.13.688387

    Figure Lengend Snippet: a) Shown here is a region of the healthy lung sample assayed using Xenium, with the boundary expansion segmentation from 10x Xenium Ranger (Top) and Proseg (Bottom) segmentation. Each dot is a transcript molecule, molecules of lineage marker genes are coloured by their respective lineages. Black lines are segmentation boundaries. b) Log CPM (counts per million) normalised pseudobulked gene expression of 4 selected contaminating genes using 4 annotated immune cell types in the lung fibrosis Xenium data. Each data point is a sample and a lowess curve is fitted over all the samples. c) A high level schematic of the application of DenoIST.

    Article Snippet: To address this research gap, we present DenoIST (Denoising Image-based Spatial Transcriptomics), a Poisson mixture model tailored for denoising IST data by reducing the effects of transcript contamination in downstream analysis tasks.

    Techniques: Marker, Gene Expression

    Expression of ACTA2 from a zoomed-in section in Xenium human breast cancer dataset. Each dot is a segmented cell using 10x boundary expansion method, colour shows the log count of ACTA2 . Cells with 0 count are greyed out for visual clarity. b) Heatmap visualisation of gene expression of annotated cell types before (top) and after DenoIST (bottom). Columns are selected genes, annotated by the cell type they mark. Row are cell types. The log(mean count + 1) for each cell type is shown here. c) MECR before (top) and after (bottom) applying DenoIST to Xenium human breast cancer dataset. Rows and columns denote genes and each entry is the MECR of the corresponding pair. Note that genes that mark the same cell type are not expected to be mutually exclusive, but are shown here for positive control.

    Journal: bioRxiv

    Article Title: Denoising image-based spatial transcriptomics data with DenoIST

    doi: 10.1101/2025.11.13.688387

    Figure Lengend Snippet: Expression of ACTA2 from a zoomed-in section in Xenium human breast cancer dataset. Each dot is a segmented cell using 10x boundary expansion method, colour shows the log count of ACTA2 . Cells with 0 count are greyed out for visual clarity. b) Heatmap visualisation of gene expression of annotated cell types before (top) and after DenoIST (bottom). Columns are selected genes, annotated by the cell type they mark. Row are cell types. The log(mean count + 1) for each cell type is shown here. c) MECR before (top) and after (bottom) applying DenoIST to Xenium human breast cancer dataset. Rows and columns denote genes and each entry is the MECR of the corresponding pair. Note that genes that mark the same cell type are not expected to be mutually exclusive, but are shown here for positive control.

    Article Snippet: To address this research gap, we present DenoIST (Denoising Image-based Spatial Transcriptomics), a Poisson mixture model tailored for denoising IST data by reducing the effects of transcript contamination in downstream analysis tasks.

    Techniques: Expressing, Gene Expression, Positive Control

    a) UMAP visualisation of lung fibrosis data after applying DenoIST. Sample TILD028MA is shown here. Cells with 0 count are greyed out for visual clarity. b) An airway section from fibrotic sample VUILD110. Each dot is a cell. Cells with 0 count are greyed out for visual clarity. Annotated airway cell types and gene expression (raw counts and DenoIST-adjusted counts) for KRT5 and MUC5B are shown. c) Proportions of RCTD classification using raw counts and DenoIST-adjusted counts in healthy sample VUHD116A. d) RCTD assignment weights of the second highest lineage of each cell in healthy sample VUHD116A, stratified by their manually annotated lineages. Cells with a pure identity should have low weights for the incorrect lineages.

    Journal: bioRxiv

    Article Title: Denoising image-based spatial transcriptomics data with DenoIST

    doi: 10.1101/2025.11.13.688387

    Figure Lengend Snippet: a) UMAP visualisation of lung fibrosis data after applying DenoIST. Sample TILD028MA is shown here. Cells with 0 count are greyed out for visual clarity. b) An airway section from fibrotic sample VUILD110. Each dot is a cell. Cells with 0 count are greyed out for visual clarity. Annotated airway cell types and gene expression (raw counts and DenoIST-adjusted counts) for KRT5 and MUC5B are shown. c) Proportions of RCTD classification using raw counts and DenoIST-adjusted counts in healthy sample VUHD116A. d) RCTD assignment weights of the second highest lineage of each cell in healthy sample VUHD116A, stratified by their manually annotated lineages. Cells with a pure identity should have low weights for the incorrect lineages.

    Article Snippet: To address this research gap, we present DenoIST (Denoising Image-based Spatial Transcriptomics), a Poisson mixture model tailored for denoising IST data by reducing the effects of transcript contamination in downstream analysis tasks.

    Techniques: Gene Expression