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imaris image segmentation analysis  (Oxford Instruments)


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    Structured Review

    Oxford Instruments imaris image segmentation analysis
    Imaris Image Segmentation Analysis, supplied by Oxford Instruments, used in various techniques. Bioz Stars score: 99/100, based on 44474 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/image+segmentation/Imaris/pm41387458-114-8-8
    Average 99 stars, based on 44474 article reviews
    imaris image segmentation analysis - by Bioz Stars, 2026-10
    99/100 stars

    Images

    Related Articles

    Software:

    Article Title: Morphological plasticity facilitates lung adaptation and dynamic immune remodeling in Mycobacterium abscessus infection
    Article Snippet: .. To quantify bacterial internalization versus extracellular adherence, z-stack images (step size: 0.3 μm) were acquired and subjected to 3D volumetric reconstruction using Imaris v9.5 software. ..

    Article Title: Chrysanthemum Morifolium– Derived Nanovesicles Reduce Lactate‐Associated Histone Lactylation and Modulate Microglia‐Mediated Neuroinflammation in Sepsis‐Associated Encephalopathy
    Article Snippet: An excitation wavelength of 488 nm and emission wavelength of 519 nm were employed to visualize the Iba‐1 protein. .. Images of microglial branch nodes (1024 × 1024 pixel) and total branch length were reconstructed and quantitatively analyzed using the “Filaments” module of the Imaris 10.1.0 software. ..

    Morphology:

    Article Title: Frontal cortical neuroinflammation and circulating biomarkers following cardiopulmonary bypass in sheep.
    Article Snippet: Images were acquired using the Nikon-Crest Spinning Disk Confocal microscope, at 40× magnification (objective Plan-Apochromat, 40×/1.25, silicone), with the systemrecommended 0.35 μm step size for a z-stack size of 20.1 μm. .. Microglial morphology was analysed in Imaris v10.2 (Oxford Instruments, Abingdon, UK) [30]. ..

    other:

    Article Title: Multiple motor proteins regulate TDP-43 anterograde axonal transport.
    Article Snippet: a—top Representative micrographs of particles movement, segmentation and tracking determined with Imaris spots tracking algorithms.



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    <t>UW-Madison</t> <t>GI</t> tract dataset.
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    Oxford Instruments f k imaris 3d image segmentation
    a A <t>3D</t> Z-stack confocal image taken by ZEISS Airyscan confocal super-resolution microscopy to demonstrate the interaction of a HIPA (wide open arrow) with neuronal somas (filled arrow). <t>b</t> <t>Imaris</t> AI software removed the Gal3 signals and created solid green surfaces of NeuN signals to demonstrate the neuronal somas. c Imaris created solid surfaces of Gal3 signals (pink) and NeuN signals (green) to demonstrate the neuronal somas (open arrows) enwrapped by the processes of a HIPA (pink). d A view of image ( c ) from a different angle. e Shown here were two representative HIPAs (red) (open wide arrows) in close interactions with neurons (green) (thin arrows). f – k Imaris 3D image segmentation of the selected area in ( e ). This image analysis removed all the signals that were not interact with HIPAs to visualize NeuN signals engulfed by HIPAs. f – h Imaris image segmentations of one region in ( e ) to show intact neuronal somas (thin white arrows) engulfed by a HIPA. i – k Imaris image segmentations of another region in ( e ) to show neuronal debris (thin red arrows) inside a HIPA. The engulfed neuronal somas revealed by creating the solid opaque surfaces (open arrow) ( f and i ), transparent surfaces (open arrow) ( g and j ), and by removing HIPA components ( h and k ). l Fraction of Gal3+ astrocytes with phagocyted neuronal components. Wt: n = 3 (male); gp120Tg: n = 3 (male); paired two-tail t test; Box-and-whisker plots were generated in Microsoft Excel; boxes represent the interquartile range (25th–75th percentiles), the center line indicates the median, whiskers extend to data points within 1.5× the interquartile range. m Combination of Fluoro-Jade C (FJC) staining and Gal3 IF staining revealed extensive overlap (arrows) of degenerative neurons revealed by FJC staining and HIPAs revealed by Gal3 IF staining. The experiment was independently repeated 3 times. n Quantification of FJC staining signals in the WT and gp120Tg spinal cords. Wt: n = 4 (male); gp120Tg : n = 5 (male); unpaired t two-tail test with Welch’s correction; Data are presented as mean ± SEM.
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    Image Search Results


    UW-Madison GI tract dataset.

    Journal: Scientific Reports

    Article Title: Multi-level attention DeepLab V3+ with EfficientNetB0 for GI tract organ segmentation in MRI scans

    doi: 10.1038/s41598-026-38247-7

    Figure Lengend Snippet: UW-Madison GI tract dataset.

    Article Snippet: The dataset used in this study, the “UW-Madison GI Tract Image Segmentation” dataset, is publicly available on Kaggle.

    Techniques:

    UW-Madison dataset ( a ) input image, ( b ) RLE decoded for large bowel, ( c ) RLE decoded for small bowel, and ( d ) RLE decoded for stomach.

    Journal: Scientific Reports

    Article Title: Multi-level attention DeepLab V3+ with EfficientNetB0 for GI tract organ segmentation in MRI scans

    doi: 10.1038/s41598-026-38247-7

    Figure Lengend Snippet: UW-Madison dataset ( a ) input image, ( b ) RLE decoded for large bowel, ( c ) RLE decoded for small bowel, and ( d ) RLE decoded for stomach.

    Article Snippet: The dataset used in this study, the “UW-Madison GI Tract Image Segmentation” dataset, is publicly available on Kaggle.

    Techniques:

    a A 3D Z-stack confocal image taken by ZEISS Airyscan confocal super-resolution microscopy to demonstrate the interaction of a HIPA (wide open arrow) with neuronal somas (filled arrow). b Imaris AI software removed the Gal3 signals and created solid green surfaces of NeuN signals to demonstrate the neuronal somas. c Imaris created solid surfaces of Gal3 signals (pink) and NeuN signals (green) to demonstrate the neuronal somas (open arrows) enwrapped by the processes of a HIPA (pink). d A view of image ( c ) from a different angle. e Shown here were two representative HIPAs (red) (open wide arrows) in close interactions with neurons (green) (thin arrows). f – k Imaris 3D image segmentation of the selected area in ( e ). This image analysis removed all the signals that were not interact with HIPAs to visualize NeuN signals engulfed by HIPAs. f – h Imaris image segmentations of one region in ( e ) to show intact neuronal somas (thin white arrows) engulfed by a HIPA. i – k Imaris image segmentations of another region in ( e ) to show neuronal debris (thin red arrows) inside a HIPA. The engulfed neuronal somas revealed by creating the solid opaque surfaces (open arrow) ( f and i ), transparent surfaces (open arrow) ( g and j ), and by removing HIPA components ( h and k ). l Fraction of Gal3+ astrocytes with phagocyted neuronal components. Wt: n = 3 (male); gp120Tg: n = 3 (male); paired two-tail t test; Box-and-whisker plots were generated in Microsoft Excel; boxes represent the interquartile range (25th–75th percentiles), the center line indicates the median, whiskers extend to data points within 1.5× the interquartile range. m Combination of Fluoro-Jade C (FJC) staining and Gal3 IF staining revealed extensive overlap (arrows) of degenerative neurons revealed by FJC staining and HIPAs revealed by Gal3 IF staining. The experiment was independently repeated 3 times. n Quantification of FJC staining signals in the WT and gp120Tg spinal cords. Wt: n = 4 (male); gp120Tg : n = 5 (male); unpaired t two-tail test with Welch’s correction; Data are presented as mean ± SEM.

    Journal: Nature Communications

    Article Title: Identification of a reactive astrocyte subpopulation during HIV-associated pain pathogenesis in mouse models

    doi: 10.1038/s41467-025-67368-2

    Figure Lengend Snippet: a A 3D Z-stack confocal image taken by ZEISS Airyscan confocal super-resolution microscopy to demonstrate the interaction of a HIPA (wide open arrow) with neuronal somas (filled arrow). b Imaris AI software removed the Gal3 signals and created solid green surfaces of NeuN signals to demonstrate the neuronal somas. c Imaris created solid surfaces of Gal3 signals (pink) and NeuN signals (green) to demonstrate the neuronal somas (open arrows) enwrapped by the processes of a HIPA (pink). d A view of image ( c ) from a different angle. e Shown here were two representative HIPAs (red) (open wide arrows) in close interactions with neurons (green) (thin arrows). f – k Imaris 3D image segmentation of the selected area in ( e ). This image analysis removed all the signals that were not interact with HIPAs to visualize NeuN signals engulfed by HIPAs. f – h Imaris image segmentations of one region in ( e ) to show intact neuronal somas (thin white arrows) engulfed by a HIPA. i – k Imaris image segmentations of another region in ( e ) to show neuronal debris (thin red arrows) inside a HIPA. The engulfed neuronal somas revealed by creating the solid opaque surfaces (open arrow) ( f and i ), transparent surfaces (open arrow) ( g and j ), and by removing HIPA components ( h and k ). l Fraction of Gal3+ astrocytes with phagocyted neuronal components. Wt: n = 3 (male); gp120Tg: n = 3 (male); paired two-tail t test; Box-and-whisker plots were generated in Microsoft Excel; boxes represent the interquartile range (25th–75th percentiles), the center line indicates the median, whiskers extend to data points within 1.5× the interquartile range. m Combination of Fluoro-Jade C (FJC) staining and Gal3 IF staining revealed extensive overlap (arrows) of degenerative neurons revealed by FJC staining and HIPAs revealed by Gal3 IF staining. The experiment was independently repeated 3 times. n Quantification of FJC staining signals in the WT and gp120Tg spinal cords. Wt: n = 4 (male); gp120Tg : n = 5 (male); unpaired t two-tail test with Welch’s correction; Data are presented as mean ± SEM.

    Article Snippet: Fig. 5 HIPAs engulfed neuronal soma in the gp120Tg spinal cord. a A 3D Z-stack confocal image taken by ZEISS Airyscan confocal super-resolution microscopy to demonstrate the interaction of a HIPA (wide open arrow) with neuronal somas (filled arrow). b Imaris AI software removed the Gal3 signals and created solid green surfaces of NeuN signals to demonstrate the neuronal somas. c Imaris created solid surfaces of Gal3 signals (pink) and NeuN signals (green) to demonstrate the neuronal somas (open arrows) enwrapped by the processes of a HIPA (pink). d A view of image ( c ) from a different angle. e Shown here were two representative HIPAs (red) (open wide arrows) in close interactions with neurons (green) (thin arrows). f – k Imaris 3D image segmentation of the selected area in ( e ).

    Techniques: Super-Resolution Microscopy, Software, Whisker Assay, Generated, Staining