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matlab-enabled 'colocalize spots' function  (MathWorks Inc)


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    MathWorks Inc matlab-enabled 'colocalize spots' function
    Matlab Enabled 'Colocalize Spots' Function, supplied by MathWorks 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/product/spots+colocalization+function/pm38216650-366-16-13
    Average 90 stars, based on 1 article reviews
    matlab-enabled 'colocalize spots' function - by Bioz Stars, 2026-09
    90/100 stars

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    Related Articles

    other:

    Article Title: Effect of extracorporeal circulation on structure of main components of animal plasma - ATR-IR and 2D-COS studies: Part I.
    Article Snippet: • Examination of animal plasma during ECC by ATR-IR and 2D-COS

    Article Title: On the potential sources of a low-frequency sound percept only a few can hear
    Article Snippet: To achieve this, the CG1 hearing thresholds were fitted with a polynomial function (3 rd order, red line in ; MatLab’s “polyfit” function was used) to obtain an extra- and interpolated LFHT.

    Article Title: Improved estimation of forage nitrogen in alpine grassland by integrating Sentinel-2 and SIF data.
    Article Snippet: For this study, the GPR model was constructed using MATLAB 2022a’s “fitrgp” function (Math Works, USA), which employs a “matern32” as its kernel function.

    Article Title: Iterative Forecasting of Financial Time Series: The Greek Stock Market from 2019 to 2024
    Article Snippet: Sequences of fBm are created using Matlab’s built-in function wfBm(H,k) with zero mean, variance 1, Hurst exponent H , and length k [ ].

    Article Title: Iterative Forecasting of Financial Time Series: The Greek Stock Market from 2019 to 2024.
    Article Snippet: Sequences of fBm are created using Matlab’s built-in function wfBm(H,k) with zero mean, variance 1, Hurst exponent H, and length k [62].

    Article Title: Quantifying axonal features of human superficial white matter from three-dimensional multibeam serial electron microscopy data assisted by deep learning.
    Article Snippet: To quantify g-ratios (i.e., the ratio of the inner to outer axon diameter), adjacent myelinated axons with contact of their myelin sheaths were first automatically segmented using a non-weighted distance transform (i.e., MATLAB’s “bwdist” function) and watershed algorithm (i.e., MATLAB’s “watershed” function) on the CNN-segmented IAS masks.

    Article Title: Optimal social distancing in pandemic preparedness and lessons from COVID-19: Intervention intensity and infective travelers.
    Article Snippet: Our analysis seeks best social distancing strategies optimally balancing the direct costs of a threatening outbreak with its societal-level costs by investigating the effects of different levels of restrictions’ intensity and of the continued importation of infective travellers, while controlling for the key dimensions of the response, such as early action, adherence and the relative weight of societal costs.. We identify two primary degrees of freedom in epidemic control, namely the maximum intensity of control measures and their duration.. In the absence of travellers, a lower (higher) maximum intensity requires a longer (shorter) duration to achieve similar control outcomes.

    Article Title: Fetal heart rate variability in relation to maternal physical activity and metabolic health.
    Article Snippet: We then plotted the variance explained by the components and retained the first n components preceding the inflection point on the Scree plot, identified using Matlab’s `findchangepts` function (configured with ‘statistic’ = mean, ‘MaxNumChanges’ = 1).



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    The nuclear translocation of S protein and S mRNA includes both the outer surface and inside of the nucleus. Separate slides (see ) were imaged under a Leica Stellaris confocal microscope (Leica) using a 63x oil objective. The images were then deconvolved using Huygen Essential deconvolution software (Scientific Volume Imaging). Using the surface rendering function of an image processing IMARIS software. (A) S mRNA (red) on the nuclear surface (top) and inside the nucleus (bottom). White arrows indicate S protein on the nuclear surface (top image) or inside the nucleus (bottom image). (B) S protein (green) on the nuclear surface (top image) and inside the nucleus (bottom image). White arrows indicate S protein on the nuclear surface (top image) or inside the nucleus (bottom image). (C) The total distribution of S mRNA and S protein in the cells. The data were obtained by combining multiple images from an independent experiment. (D) The total <t>colocalization</t> between S mRNA and S protein in the cells. The data were obtained by combining multiple images from an independent experiment.
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    The nuclear translocation of S protein and S mRNA includes both the outer surface and inside of the nucleus. Separate slides (see ) were imaged under a Leica Stellaris confocal microscope (Leica) using a 63x oil objective. The images were then deconvolved using Huygen Essential deconvolution software (Scientific Volume Imaging). Using the surface rendering function of an image processing IMARIS software. (A) S mRNA (red) on the nuclear surface (top) and inside the nucleus (bottom). White arrows indicate S protein on the nuclear surface (top image) or inside the nucleus (bottom image). (B) S protein (green) on the nuclear surface (top image) and inside the nucleus (bottom image). White arrows indicate S protein on the nuclear surface (top image) or inside the nucleus (bottom image). (C) The total distribution of S mRNA and S protein in the cells. The data were obtained by combining multiple images from an independent experiment. (D) The total <t>colocalization</t> between S mRNA and S protein in the cells. The data were obtained by combining multiple images from an independent experiment.
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    Image Search Results


    The nuclear translocation of S protein and S mRNA includes both the outer surface and inside of the nucleus. Separate slides (see ) were imaged under a Leica Stellaris confocal microscope (Leica) using a 63x oil objective. The images were then deconvolved using Huygen Essential deconvolution software (Scientific Volume Imaging). Using the surface rendering function of an image processing IMARIS software. (A) S mRNA (red) on the nuclear surface (top) and inside the nucleus (bottom). White arrows indicate S protein on the nuclear surface (top image) or inside the nucleus (bottom image). (B) S protein (green) on the nuclear surface (top image) and inside the nucleus (bottom image). White arrows indicate S protein on the nuclear surface (top image) or inside the nucleus (bottom image). (C) The total distribution of S mRNA and S protein in the cells. The data were obtained by combining multiple images from an independent experiment. (D) The total colocalization between S mRNA and S protein in the cells. The data were obtained by combining multiple images from an independent experiment.

    Journal: Frontiers in Microbiology

    Article Title: Nuclear translocation of spike mRNA and protein is a novel feature of SARS-CoV-2

    doi: 10.3389/fmicb.2023.1073789

    Figure Lengend Snippet: The nuclear translocation of S protein and S mRNA includes both the outer surface and inside of the nucleus. Separate slides (see ) were imaged under a Leica Stellaris confocal microscope (Leica) using a 63x oil objective. The images were then deconvolved using Huygen Essential deconvolution software (Scientific Volume Imaging). Using the surface rendering function of an image processing IMARIS software. (A) S mRNA (red) on the nuclear surface (top) and inside the nucleus (bottom). White arrows indicate S protein on the nuclear surface (top image) or inside the nucleus (bottom image). (B) S protein (green) on the nuclear surface (top image) and inside the nucleus (bottom image). White arrows indicate S protein on the nuclear surface (top image) or inside the nucleus (bottom image). (C) The total distribution of S mRNA and S protein in the cells. The data were obtained by combining multiple images from an independent experiment. (D) The total colocalization between S mRNA and S protein in the cells. The data were obtained by combining multiple images from an independent experiment.

    Article Snippet: To confirm the physical apposition between S mRNA and the nucleus by comparing their distributions in fluorescent images, we used the spot-to-spot colocalization function in Imaris image analysis software (Oxford Instruments).

    Techniques: Translocation Assay, Microscopy, Software, Imaging

    Colocalization between S mRNA and S protein inside infected cells. The images (see ) were analyzed by using the surface rendering and colocalization features of IMARIS. S protein and S mRNA distribution and colocalization in the cytoplasm (top panel), on the nuclear surface (middle panel) and inside the nucleus (bottom panel). The specific region of colocalization is indicated by a white spot. Scale bar 0.5 μm.

    Journal: Frontiers in Microbiology

    Article Title: Nuclear translocation of spike mRNA and protein is a novel feature of SARS-CoV-2

    doi: 10.3389/fmicb.2023.1073789

    Figure Lengend Snippet: Colocalization between S mRNA and S protein inside infected cells. The images (see ) were analyzed by using the surface rendering and colocalization features of IMARIS. S protein and S mRNA distribution and colocalization in the cytoplasm (top panel), on the nuclear surface (middle panel) and inside the nucleus (bottom panel). The specific region of colocalization is indicated by a white spot. Scale bar 0.5 μm.

    Article Snippet: To confirm the physical apposition between S mRNA and the nucleus by comparing their distributions in fluorescent images, we used the spot-to-spot colocalization function in Imaris image analysis software (Oxford Instruments).

    Techniques: Infection