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comstat matlab package  (MathWorks Inc)


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    Structured Review

    MathWorks Inc comstat matlab package
    FleQ contributes to biofilm formation in a manner independent of SagS and SagS downstream signaling. ( A ) Representative confocal images of 3-day-old biofilms formed by P. aeruginosa PAO1, Δ fleQ, and double mutant Δ fleQΔsagS . White bar = 100 µm. ( B ) Quantitative of the biofilm biomass and biofilm height by <t>COMSTAT</t> of biofilms formed by P. aeruginosa PAO1, Δ fleQ, and double mutant Δ fleQΔsagS. * *, ***, significantly different ( P = 0.0001, <0.0001, respectively) relative to PAO1 using ANOVA followed by the Bartlett’s test. Ns, not significant. ( C ) Total cellular c-di-GMP levels in 6-day-old biofilms formed by P. aeruginosa PAO1, Δ fleQ, and ΔsagS, as determined by HPLC quantitative analysis, followed by normalization relative to total cell protein content. *, P < 0.05, relative to PAO1 using ANOVA followed by Dunnett’s T3 multiple comparisons test. ( D ) Representative confocal images of 6-day-old P. aeruginosa Δ fleQ and ΔsagS biofilms and mutant biofilms expressing bfiR and gcbA. gcbA encodes diguanylate cyclase GcbA, bfiR the two-component response regulator BfiR. White bar = 100 µm. All experiments were performed in triplicate. Error bars indicate standard deviations.
    Comstat Matlab Package, 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
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    Images

    1) Product Images from "FleQ finetunes the expression of a subset of BrlR-activated genes to enable antibiotic tolerance by Pseudomonas aeruginosa biofilms"

    Article Title: FleQ finetunes the expression of a subset of BrlR-activated genes to enable antibiotic tolerance by Pseudomonas aeruginosa biofilms

    Journal: Journal of Bacteriology

    doi: 10.1128/jb.00503-24

    FleQ contributes to biofilm formation in a manner independent of SagS and SagS downstream signaling. ( A ) Representative confocal images of 3-day-old biofilms formed by P. aeruginosa PAO1, Δ fleQ, and double mutant Δ fleQΔsagS . White bar = 100 µm. ( B ) Quantitative of the biofilm biomass and biofilm height by COMSTAT of biofilms formed by P. aeruginosa PAO1, Δ fleQ, and double mutant Δ fleQΔsagS. * *, ***, significantly different ( P = 0.0001, <0.0001, respectively) relative to PAO1 using ANOVA followed by the Bartlett’s test. Ns, not significant. ( C ) Total cellular c-di-GMP levels in 6-day-old biofilms formed by P. aeruginosa PAO1, Δ fleQ, and ΔsagS, as determined by HPLC quantitative analysis, followed by normalization relative to total cell protein content. *, P < 0.05, relative to PAO1 using ANOVA followed by Dunnett’s T3 multiple comparisons test. ( D ) Representative confocal images of 6-day-old P. aeruginosa Δ fleQ and ΔsagS biofilms and mutant biofilms expressing bfiR and gcbA. gcbA encodes diguanylate cyclase GcbA, bfiR the two-component response regulator BfiR. White bar = 100 µm. All experiments were performed in triplicate. Error bars indicate standard deviations.
    Figure Legend Snippet: FleQ contributes to biofilm formation in a manner independent of SagS and SagS downstream signaling. ( A ) Representative confocal images of 3-day-old biofilms formed by P. aeruginosa PAO1, Δ fleQ, and double mutant Δ fleQΔsagS . White bar = 100 µm. ( B ) Quantitative of the biofilm biomass and biofilm height by COMSTAT of biofilms formed by P. aeruginosa PAO1, Δ fleQ, and double mutant Δ fleQΔsagS. * *, ***, significantly different ( P = 0.0001, <0.0001, respectively) relative to PAO1 using ANOVA followed by the Bartlett’s test. Ns, not significant. ( C ) Total cellular c-di-GMP levels in 6-day-old biofilms formed by P. aeruginosa PAO1, Δ fleQ, and ΔsagS, as determined by HPLC quantitative analysis, followed by normalization relative to total cell protein content. *, P < 0.05, relative to PAO1 using ANOVA followed by Dunnett’s T3 multiple comparisons test. ( D ) Representative confocal images of 6-day-old P. aeruginosa Δ fleQ and ΔsagS biofilms and mutant biofilms expressing bfiR and gcbA. gcbA encodes diguanylate cyclase GcbA, bfiR the two-component response regulator BfiR. White bar = 100 µm. All experiments were performed in triplicate. Error bars indicate standard deviations.

    Techniques Used: Mutagenesis, Expressing

    Related Articles

    Software:

    Article Title: Optimal surface estimation and thresholding of confocal microscope images of biofilms using Beer's Law.
    Article Snippet: .. There are a number of automatic threshold detection schemes already available in image analysis software such as COMSTAT (implemented in MATLAB) (Heydorn et al., 2000), COMSTAT2 (implemented in ImageJ) (Vorregaard, 2008), Imaris (Imaris, 2018), and daime (Daims et al., 2006). .. Otsu's method for threshold selection, used by the COMSTAT implementations in MATLAB and ImageJ, maximizes the intra-class correlation (Otsu, 1979), where each class is composed of pixels with intensities either above or below the threshold.

    Article Title: Assessment of the bacterial viability of chlorine- and quaternary ammonium compounds-treated Lactobacillus cells via a multi-method approach.
    Article Snippet: Aims: The assessment of the bacterial viability of chlorineand QACs-treated Lactobacillus cells with the culture-dependent and -independent methods.. Methods and Results: Lactobacillus isolates (L. plantarum G1, L. plantarum B1, L. brevis S1, and L. paracasei W1) in biofilm and planktonic cell suspensions were treated with chlorine-based (0∙018% and 0∙18%) and quaternary ammonium compounds (QACs)-based (0∙2% and 2∙0%) disinfectants for 5 min and then analyzed by plate counting, flow cytometry (FCM), and fluorescence activated cell sorting (FACS).. The reaction of sessile cells to disinfectants was assessed with the confocal laser scanning microscopy (CLSM).

    Control:

    Article Title: The effect of Er:YAG laser treatment on biofilm formation on titanium and zirconia disc surfaces
    Article Snippet: The biofilm quantitative parameters (live-to-dead bacteria ratio, structure biomass, and average thickness) were first tested for data normality; then the comparison of these biofilm parameters between the †† LIVE/DEAD BacLight dye kit, Thermo Fisher Scientific, Waltham, MA, USA ‡‡ FV 1000: Olympus, Tokyo, Japan. .. §§ http://www.imageanalysis.dk *** COMSTAT, The MathWorks Inc., Natick, MA, USA ††† IBM Co., Armonk, NY, USA control and laser treatment groups was assessed via the ttest for normally distributed data and the Mann-Whitney U test for non-normal data. ..

    Mann-Whitney U-Test:

    Article Title: The effect of Er:YAG laser treatment on biofilm formation on titanium and zirconia disc surfaces
    Article Snippet: The biofilm quantitative parameters (live-to-dead bacteria ratio, structure biomass, and average thickness) were first tested for data normality; then the comparison of these biofilm parameters between the †† LIVE/DEAD BacLight dye kit, Thermo Fisher Scientific, Waltham, MA, USA ‡‡ FV 1000: Olympus, Tokyo, Japan. .. §§ http://www.imageanalysis.dk *** COMSTAT, The MathWorks Inc., Natick, MA, USA ††† IBM Co., Armonk, NY, USA control and laser treatment groups was assessed via the ttest for normally distributed data and the Mann-Whitney U test for non-normal data. ..



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    FleQ contributes to biofilm formation in a manner independent of SagS and SagS downstream signaling. ( A ) Representative confocal images of 3-day-old biofilms formed by P. aeruginosa PAO1, Δ fleQ, and double mutant Δ fleQΔsagS . White bar = 100 µm. ( B ) Quantitative of the biofilm biomass and biofilm height by <t>COMSTAT</t> of biofilms formed by P. aeruginosa PAO1, Δ fleQ, and double mutant Δ fleQΔsagS. * *, ***, significantly different ( P = 0.0001, <0.0001, respectively) relative to PAO1 using ANOVA followed by the Bartlett’s test. Ns, not significant. ( C ) Total cellular c-di-GMP levels in 6-day-old biofilms formed by P. aeruginosa PAO1, Δ fleQ, and ΔsagS, as determined by HPLC quantitative analysis, followed by normalization relative to total cell protein content. *, P < 0.05, relative to PAO1 using ANOVA followed by Dunnett’s T3 multiple comparisons test. ( D ) Representative confocal images of 6-day-old P. aeruginosa Δ fleQ and ΔsagS biofilms and mutant biofilms expressing bfiR and gcbA. gcbA encodes diguanylate cyclase GcbA, bfiR the two-component response regulator BfiR. White bar = 100 µm. All experiments were performed in triplicate. Error bars indicate standard deviations.
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    FleQ contributes to biofilm formation in a manner independent of SagS and SagS downstream signaling. ( A ) Representative confocal images of 3-day-old biofilms formed by P. aeruginosa PAO1, Δ fleQ, and double mutant Δ fleQΔsagS . White bar = 100 µm. ( B ) Quantitative of the biofilm biomass and biofilm height by <t>COMSTAT</t> of biofilms formed by P. aeruginosa PAO1, Δ fleQ, and double mutant Δ fleQΔsagS. * *, ***, significantly different ( P = 0.0001, <0.0001, respectively) relative to PAO1 using ANOVA followed by the Bartlett’s test. Ns, not significant. ( C ) Total cellular c-di-GMP levels in 6-day-old biofilms formed by P. aeruginosa PAO1, Δ fleQ, and ΔsagS, as determined by HPLC quantitative analysis, followed by normalization relative to total cell protein content. *, P < 0.05, relative to PAO1 using ANOVA followed by Dunnett’s T3 multiple comparisons test. ( D ) Representative confocal images of 6-day-old P. aeruginosa Δ fleQ and ΔsagS biofilms and mutant biofilms expressing bfiR and gcbA. gcbA encodes diguanylate cyclase GcbA, bfiR the two-component response regulator BfiR. White bar = 100 µm. All experiments were performed in triplicate. Error bars indicate standard deviations.
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    FleQ contributes to biofilm formation in a manner independent of SagS and SagS downstream signaling. ( A ) Representative confocal images of 3-day-old biofilms formed by P. aeruginosa PAO1, Δ fleQ, and double mutant Δ fleQΔsagS . White bar = 100 µm. ( B ) Quantitative of the biofilm biomass and biofilm height by <t>COMSTAT</t> of biofilms formed by P. aeruginosa PAO1, Δ fleQ, and double mutant Δ fleQΔsagS. * *, ***, significantly different ( P = 0.0001, <0.0001, respectively) relative to PAO1 using ANOVA followed by the Bartlett’s test. Ns, not significant. ( C ) Total cellular c-di-GMP levels in 6-day-old biofilms formed by P. aeruginosa PAO1, Δ fleQ, and ΔsagS, as determined by HPLC quantitative analysis, followed by normalization relative to total cell protein content. *, P < 0.05, relative to PAO1 using ANOVA followed by Dunnett’s T3 multiple comparisons test. ( D ) Representative confocal images of 6-day-old P. aeruginosa Δ fleQ and ΔsagS biofilms and mutant biofilms expressing bfiR and gcbA. gcbA encodes diguanylate cyclase GcbA, bfiR the two-component response regulator BfiR. White bar = 100 µm. All experiments were performed in triplicate. Error bars indicate standard deviations.
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    FleQ contributes to biofilm formation in a manner independent of SagS and SagS downstream signaling. ( A ) Representative confocal images of 3-day-old biofilms formed by P. aeruginosa PAO1, Δ fleQ, and double mutant Δ fleQΔsagS . White bar = 100 µm. ( B ) Quantitative of the biofilm biomass and biofilm height by <t>COMSTAT</t> of biofilms formed by P. aeruginosa PAO1, Δ fleQ, and double mutant Δ fleQΔsagS. * *, ***, significantly different ( P = 0.0001, <0.0001, respectively) relative to PAO1 using ANOVA followed by the Bartlett’s test. Ns, not significant. ( C ) Total cellular c-di-GMP levels in 6-day-old biofilms formed by P. aeruginosa PAO1, Δ fleQ, and ΔsagS, as determined by HPLC quantitative analysis, followed by normalization relative to total cell protein content. *, P < 0.05, relative to PAO1 using ANOVA followed by Dunnett’s T3 multiple comparisons test. ( D ) Representative confocal images of 6-day-old P. aeruginosa Δ fleQ and ΔsagS biofilms and mutant biofilms expressing bfiR and gcbA. gcbA encodes diguanylate cyclase GcbA, bfiR the two-component response regulator BfiR. White bar = 100 µm. All experiments were performed in triplicate. Error bars indicate standard deviations.
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    FleQ contributes to biofilm formation in a manner independent of SagS and SagS downstream signaling. ( A ) Representative confocal images of 3-day-old biofilms formed by P. aeruginosa PAO1, Δ fleQ, and double mutant Δ fleQΔsagS . White bar = 100 µm. ( B ) Quantitative of the biofilm biomass and biofilm height by <t>COMSTAT</t> of biofilms formed by P. aeruginosa PAO1, Δ fleQ, and double mutant Δ fleQΔsagS. * *, ***, significantly different ( P = 0.0001, <0.0001, respectively) relative to PAO1 using ANOVA followed by the Bartlett’s test. Ns, not significant. ( C ) Total cellular c-di-GMP levels in 6-day-old biofilms formed by P. aeruginosa PAO1, Δ fleQ, and ΔsagS, as determined by HPLC quantitative analysis, followed by normalization relative to total cell protein content. *, P < 0.05, relative to PAO1 using ANOVA followed by Dunnett’s T3 multiple comparisons test. ( D ) Representative confocal images of 6-day-old P. aeruginosa Δ fleQ and ΔsagS biofilms and mutant biofilms expressing bfiR and gcbA. gcbA encodes diguanylate cyclase GcbA, bfiR the two-component response regulator BfiR. White bar = 100 µm. All experiments were performed in triplicate. Error bars indicate standard deviations.
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    FleQ contributes to biofilm formation in a manner independent of SagS and SagS downstream signaling. ( A ) Representative confocal images of 3-day-old biofilms formed by P. aeruginosa PAO1, Δ fleQ, and double mutant Δ fleQΔsagS . White bar = 100 µm. ( B ) Quantitative of the biofilm biomass and biofilm height by <t>COMSTAT</t> of biofilms formed by P. aeruginosa PAO1, Δ fleQ, and double mutant Δ fleQΔsagS. * *, ***, significantly different ( P = 0.0001, <0.0001, respectively) relative to PAO1 using ANOVA followed by the Bartlett’s test. Ns, not significant. ( C ) Total cellular c-di-GMP levels in 6-day-old biofilms formed by P. aeruginosa PAO1, Δ fleQ, and ΔsagS, as determined by HPLC quantitative analysis, followed by normalization relative to total cell protein content. *, P < 0.05, relative to PAO1 using ANOVA followed by Dunnett’s T3 multiple comparisons test. ( D ) Representative confocal images of 6-day-old P. aeruginosa Δ fleQ and ΔsagS biofilms and mutant biofilms expressing bfiR and gcbA. gcbA encodes diguanylate cyclase GcbA, bfiR the two-component response regulator BfiR. White bar = 100 µm. All experiments were performed in triplicate. Error bars indicate standard deviations.
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    Image Search Results


    FleQ contributes to biofilm formation in a manner independent of SagS and SagS downstream signaling. ( A ) Representative confocal images of 3-day-old biofilms formed by P. aeruginosa PAO1, Δ fleQ, and double mutant Δ fleQΔsagS . White bar = 100 µm. ( B ) Quantitative of the biofilm biomass and biofilm height by COMSTAT of biofilms formed by P. aeruginosa PAO1, Δ fleQ, and double mutant Δ fleQΔsagS. * *, ***, significantly different ( P = 0.0001, <0.0001, respectively) relative to PAO1 using ANOVA followed by the Bartlett’s test. Ns, not significant. ( C ) Total cellular c-di-GMP levels in 6-day-old biofilms formed by P. aeruginosa PAO1, Δ fleQ, and ΔsagS, as determined by HPLC quantitative analysis, followed by normalization relative to total cell protein content. *, P < 0.05, relative to PAO1 using ANOVA followed by Dunnett’s T3 multiple comparisons test. ( D ) Representative confocal images of 6-day-old P. aeruginosa Δ fleQ and ΔsagS biofilms and mutant biofilms expressing bfiR and gcbA. gcbA encodes diguanylate cyclase GcbA, bfiR the two-component response regulator BfiR. White bar = 100 µm. All experiments were performed in triplicate. Error bars indicate standard deviations.

    Journal: Journal of Bacteriology

    Article Title: FleQ finetunes the expression of a subset of BrlR-activated genes to enable antibiotic tolerance by Pseudomonas aeruginosa biofilms

    doi: 10.1128/jb.00503-24

    Figure Lengend Snippet: FleQ contributes to biofilm formation in a manner independent of SagS and SagS downstream signaling. ( A ) Representative confocal images of 3-day-old biofilms formed by P. aeruginosa PAO1, Δ fleQ, and double mutant Δ fleQΔsagS . White bar = 100 µm. ( B ) Quantitative of the biofilm biomass and biofilm height by COMSTAT of biofilms formed by P. aeruginosa PAO1, Δ fleQ, and double mutant Δ fleQΔsagS. * *, ***, significantly different ( P = 0.0001, <0.0001, respectively) relative to PAO1 using ANOVA followed by the Bartlett’s test. Ns, not significant. ( C ) Total cellular c-di-GMP levels in 6-day-old biofilms formed by P. aeruginosa PAO1, Δ fleQ, and ΔsagS, as determined by HPLC quantitative analysis, followed by normalization relative to total cell protein content. *, P < 0.05, relative to PAO1 using ANOVA followed by Dunnett’s T3 multiple comparisons test. ( D ) Representative confocal images of 6-day-old P. aeruginosa Δ fleQ and ΔsagS biofilms and mutant biofilms expressing bfiR and gcbA. gcbA encodes diguanylate cyclase GcbA, bfiR the two-component response regulator BfiR. White bar = 100 µm. All experiments were performed in triplicate. Error bars indicate standard deviations.

    Article Snippet: Quantitative analysis of the images was performed using COMSTAT MATLAB package and COMSTAT2 ( , ).

    Techniques: Mutagenesis, Expressing