computer software utilities 2019b Search Results


90
OriginLab corp originpro 2019b software
Originpro 2019b Software, supplied by OriginLab corp, 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/computer+software+utilities+2019b/pm38126895-465-17-20?v=OriginLab+corp
Average 90 stars, based on 1 article reviews
originpro 2019b software - by Bioz Stars, 2026-08
90/100 stars
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99
Sartorius AG incucyte s3 software
Augmented antibody titer, viral neutralization, and lymph node retention of RBD-bann protein vaccine. RBD variants were isolated from the supernatants of mammalian cells via affinity chromatography and analyzed for purity and specificity via SDS-PAGE ( a ) and the binding of recombinant proteins at a serial dilution, or buffer alone (0), to immobilized human ACE2 receptor was measured in an ELISA assay ( b ). Dissociation of RBD and RBD-bann from immobilized hACE2 was measured by SPR ( c ). Mice were immunized with RBD and RBD-bann proteins purified from mammalian cell supernatant with/without squalene-mediated adjuvant. End point titer (EPT) for total IgG against RBD ( d – e ) and against spike protein ( f – g ). Graphs represent the mean EPTs of groups of mice ( n = 6 per group). Each dot represents an individual animal. * p < 0.05; ** p < 0.01. All p values are from the Mann–Whitney test compared to RBD group + AddaVax. Neutralization titer in mice sera was determined using a pseudovirus system. Sera of mice immunized with isolated proteins were diluted 50-fold, and Spike-pseudotyped virus infection of ACE2 and TMPRSS2-transfected HEK293 cells was followed by luminescence. Mean and SEM biological replicates are shown ( b ). * p < 0.05, *** p < 0.001, **** p < 0.0001. All p values are from one-way ANOVA followed by Tukey’s multiple comparisons test compared to the buffer group ( h ). A serum virus neutralization assay was performed by infecting Vero E6 cells with SARS-CoV-2-GFP reporter virus (MOI 1) with prior incubation of inoculum with dilutions of mouse sera (1:50) immunized with indicated isolated proteins. As control cells were left uninfected (mock), GFP signal was measured 36-h post-infection using the <t>Incucyte</t> <t>S3</t> live-cell imaging system. Each point represents the mean of two technical replicates, and the mean +/− SD from six mice per group is indicated. Indicated p -values apply for comparison between individual conditions and the dilution-matched buffer condition and were calculated using a one-sided Student’s t -test between RBD + Addaax and RBD-bann + Addavax. * p < 0.05 ( i ). Trafficking of labeled isolated proteins into the popliteal lymph nodes (PLN). AF-647 labeled RBD proteins were injected into the foot pad (RBD left, RBD-bann right). The fluorescence signal of AF-647 was determined in the popliteal lymph node, depicting the presence of labeled RBD. Each dot represents the measurement of the region of interest (ROI) of an individual animal PLN. * p < 0.05 derived from two-tailed paired t -test ( j ).
Incucyte S3 Software, supplied by Sartorius AG, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/computer+software+utilities+2019b/pmc08146944-194-8-11?v=Sartorius+AG
Average 99 stars, based on 1 article reviews
incucyte s3 software - by Bioz Stars, 2026-08
99/100 stars
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90
METTLER TOLEDO star™ software
Augmented antibody titer, viral neutralization, and lymph node retention of RBD-bann protein vaccine. RBD variants were isolated from the supernatants of mammalian cells via affinity chromatography and analyzed for purity and specificity via SDS-PAGE ( a ) and the binding of recombinant proteins at a serial dilution, or buffer alone (0), to immobilized human ACE2 receptor was measured in an ELISA assay ( b ). Dissociation of RBD and RBD-bann from immobilized hACE2 was measured by SPR ( c ). Mice were immunized with RBD and RBD-bann proteins purified from mammalian cell supernatant with/without squalene-mediated adjuvant. End point titer (EPT) for total IgG against RBD ( d – e ) and against spike protein ( f – g ). Graphs represent the mean EPTs of groups of mice ( n = 6 per group). Each dot represents an individual animal. * p < 0.05; ** p < 0.01. All p values are from the Mann–Whitney test compared to RBD group + AddaVax. Neutralization titer in mice sera was determined using a pseudovirus system. Sera of mice immunized with isolated proteins were diluted 50-fold, and Spike-pseudotyped virus infection of ACE2 and TMPRSS2-transfected HEK293 cells was followed by luminescence. Mean and SEM biological replicates are shown ( b ). * p < 0.05, *** p < 0.001, **** p < 0.0001. All p values are from one-way ANOVA followed by Tukey’s multiple comparisons test compared to the buffer group ( h ). A serum virus neutralization assay was performed by infecting Vero E6 cells with SARS-CoV-2-GFP reporter virus (MOI 1) with prior incubation of inoculum with dilutions of mouse sera (1:50) immunized with indicated isolated proteins. As control cells were left uninfected (mock), GFP signal was measured 36-h post-infection using the <t>Incucyte</t> <t>S3</t> live-cell imaging system. Each point represents the mean of two technical replicates, and the mean +/− SD from six mice per group is indicated. Indicated p -values apply for comparison between individual conditions and the dilution-matched buffer condition and were calculated using a one-sided Student’s t -test between RBD + Addaax and RBD-bann + Addavax. * p < 0.05 ( i ). Trafficking of labeled isolated proteins into the popliteal lymph nodes (PLN). AF-647 labeled RBD proteins were injected into the foot pad (RBD left, RBD-bann right). The fluorescence signal of AF-647 was determined in the popliteal lymph node, depicting the presence of labeled RBD. Each dot represents the measurement of the region of interest (ROI) of an individual animal PLN. * p < 0.05 derived from two-tailed paired t -test ( j ).
Star™ Software, supplied by METTLER TOLEDO, 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/computer+software+utilities+2019b/us12281203-455-5-5?v=METTLER+TOLEDO
Average 90 stars, based on 1 article reviews
star™ software - by Bioz Stars, 2026-08
90/100 stars
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90
OriginLab corp origin 2019 b software
Augmented antibody titer, viral neutralization, and lymph node retention of RBD-bann protein vaccine. RBD variants were isolated from the supernatants of mammalian cells via affinity chromatography and analyzed for purity and specificity via SDS-PAGE ( a ) and the binding of recombinant proteins at a serial dilution, or buffer alone (0), to immobilized human ACE2 receptor was measured in an ELISA assay ( b ). Dissociation of RBD and RBD-bann from immobilized hACE2 was measured by SPR ( c ). Mice were immunized with RBD and RBD-bann proteins purified from mammalian cell supernatant with/without squalene-mediated adjuvant. End point titer (EPT) for total IgG against RBD ( d – e ) and against spike protein ( f – g ). Graphs represent the mean EPTs of groups of mice ( n = 6 per group). Each dot represents an individual animal. * p < 0.05; ** p < 0.01. All p values are from the Mann–Whitney test compared to RBD group + AddaVax. Neutralization titer in mice sera was determined using a pseudovirus system. Sera of mice immunized with isolated proteins were diluted 50-fold, and Spike-pseudotyped virus infection of ACE2 and TMPRSS2-transfected HEK293 cells was followed by luminescence. Mean and SEM biological replicates are shown ( b ). * p < 0.05, *** p < 0.001, **** p < 0.0001. All p values are from one-way ANOVA followed by Tukey’s multiple comparisons test compared to the buffer group ( h ). A serum virus neutralization assay was performed by infecting Vero E6 cells with SARS-CoV-2-GFP reporter virus (MOI 1) with prior incubation of inoculum with dilutions of mouse sera (1:50) immunized with indicated isolated proteins. As control cells were left uninfected (mock), GFP signal was measured 36-h post-infection using the <t>Incucyte</t> <t>S3</t> live-cell imaging system. Each point represents the mean of two technical replicates, and the mean +/− SD from six mice per group is indicated. Indicated p -values apply for comparison between individual conditions and the dilution-matched buffer condition and were calculated using a one-sided Student’s t -test between RBD + Addaax and RBD-bann + Addavax. * p < 0.05 ( i ). Trafficking of labeled isolated proteins into the popliteal lymph nodes (PLN). AF-647 labeled RBD proteins were injected into the foot pad (RBD left, RBD-bann right). The fluorescence signal of AF-647 was determined in the popliteal lymph node, depicting the presence of labeled RBD. Each dot represents the measurement of the region of interest (ROI) of an individual animal PLN. * p < 0.05 derived from two-tailed paired t -test ( j ).
Origin 2019 B Software, supplied by OriginLab corp, 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/computer+software+utilities+2019b/pm36614232-330-1-5?v=OriginLab+corp
Average 90 stars, based on 1 article reviews
origin 2019 b software - by Bioz Stars, 2026-08
90/100 stars
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90
OriginLab corp heatmaps originpro 2019 b software
<t>Heatmaps</t> showing differences in macular retinal nerve fiber layer (mRNFL). Left map: this heatmap represents simple differences of mean thickness between OHT group and early POAG group in each superpixel giving an idea of the trend. Right map: the heatmap represents statistically significant differences ( p < 0.05) of the mean thickness between groups in each superpixel. No significant difference ( p ≥ 0.05) is represented in black. Range of significant OHT-POAG differences in superpixels between −20.70 and −1.35 microns.
Heatmaps Originpro 2019 B Software, supplied by OriginLab corp, 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/computer+software+utilities+2019b/pmc07290368-78-17-22?v=OriginLab+corp
Average 90 stars, based on 1 article reviews
heatmaps originpro 2019 b software - by Bioz Stars, 2026-08
90/100 stars
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90
OriginLab corp origin professional software version 2019b
<t>Heatmaps</t> showing differences in macular retinal nerve fiber layer (mRNFL). Left map: this heatmap represents simple differences of mean thickness between OHT group and early POAG group in each superpixel giving an idea of the trend. Right map: the heatmap represents statistically significant differences ( p < 0.05) of the mean thickness between groups in each superpixel. No significant difference ( p ≥ 0.05) is represented in black. Range of significant OHT-POAG differences in superpixels between −20.70 and −1.35 microns.
Origin Professional Software Version 2019b, supplied by OriginLab corp, 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/computer+software+utilities+2019b/pmc10003456-196-9-14?v=OriginLab+corp
Average 90 stars, based on 1 article reviews
origin professional software version 2019b - by Bioz Stars, 2026-08
90/100 stars
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90
GraphPad Software Inc origin 2019b
<t>Heatmaps</t> showing differences in macular retinal nerve fiber layer (mRNFL). Left map: this heatmap represents simple differences of mean thickness between OHT group and early POAG group in each superpixel giving an idea of the trend. Right map: the heatmap represents statistically significant differences ( p < 0.05) of the mean thickness between groups in each superpixel. No significant difference ( p ≥ 0.05) is represented in black. Range of significant OHT-POAG differences in superpixels between −20.70 and −1.35 microns.
Origin 2019b, supplied by GraphPad Software 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/computer+software+utilities+2019b/pmc10971632-85-21-20?v=GraphPad+Software+Inc
Average 90 stars, based on 1 article reviews
origin 2019b - by Bioz Stars, 2026-08
90/100 stars
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90
GraphPad Software Inc prism 8.0.2
<t>Heatmaps</t> showing differences in macular retinal nerve fiber layer (mRNFL). Left map: this heatmap represents simple differences of mean thickness between OHT group and early POAG group in each superpixel giving an idea of the trend. Right map: the heatmap represents statistically significant differences ( p < 0.05) of the mean thickness between groups in each superpixel. No significant difference ( p ≥ 0.05) is represented in black. Range of significant OHT-POAG differences in superpixels between −20.70 and −1.35 microns.
Prism 8.0.2, supplied by GraphPad Software 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/computer+software+utilities+2019b/pmc10116824-197-12-11?v=GraphPad+Software+Inc
Average 90 stars, based on 1 article reviews
prism 8.0.2 - by Bioz Stars, 2026-08
90/100 stars
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90
ANSYS inc lumerical 2019b software
<t>Heatmaps</t> showing differences in macular retinal nerve fiber layer (mRNFL). Left map: this heatmap represents simple differences of mean thickness between OHT group and early POAG group in each superpixel giving an idea of the trend. Right map: the heatmap represents statistically significant differences ( p < 0.05) of the mean thickness between groups in each superpixel. No significant difference ( p ≥ 0.05) is represented in black. Range of significant OHT-POAG differences in superpixels between −20.70 and −1.35 microns.
Lumerical 2019b Software, supplied by ANSYS 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/computer+software+utilities+2019b/ppr0444743-164-1-4?v=ANSYS+inc
Average 90 stars, based on 1 article reviews
lumerical 2019b software - by Bioz Stars, 2026-08
90/100 stars
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90
Esri inc gis software
<t>Heatmaps</t> showing differences in macular retinal nerve fiber layer (mRNFL). Left map: this heatmap represents simple differences of mean thickness between OHT group and early POAG group in each superpixel giving an idea of the trend. Right map: the heatmap represents statistically significant differences ( p < 0.05) of the mean thickness between groups in each superpixel. No significant difference ( p ≥ 0.05) is represented in black. Range of significant OHT-POAG differences in superpixels between −20.70 and −1.35 microns.
Gis Software, supplied by Esri 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/computer+software+utilities+2019b/10__1002_slash_aws2__1179-147-6-9?v=Esri+inc
Average 90 stars, based on 1 article reviews
gis software - by Bioz Stars, 2026-08
90/100 stars
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96
MathWorks Inc matlab software scripts
<t>Heatmaps</t> showing differences in macular retinal nerve fiber layer (mRNFL). Left map: this heatmap represents simple differences of mean thickness between OHT group and early POAG group in each superpixel giving an idea of the trend. Right map: the heatmap represents statistically significant differences ( p < 0.05) of the mean thickness between groups in each superpixel. No significant difference ( p ≥ 0.05) is represented in black. Range of significant OHT-POAG differences in superpixels between −20.70 and −1.35 microns.
Matlab Software Scripts, supplied by MathWorks Inc, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/computer+software+utilities+2019b/pmc11514974-135-6-11?v=MathWorks+Inc
Average 96 stars, based on 1 article reviews
matlab software scripts - by Bioz Stars, 2026-08
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98
MathWorks Inc spike2 software into matlab
<t>Heatmaps</t> showing differences in macular retinal nerve fiber layer (mRNFL). Left map: this heatmap represents simple differences of mean thickness between OHT group and early POAG group in each superpixel giving an idea of the trend. Right map: the heatmap represents statistically significant differences ( p < 0.05) of the mean thickness between groups in each superpixel. No significant difference ( p ≥ 0.05) is represented in black. Range of significant OHT-POAG differences in superpixels between −20.70 and −1.35 microns.
Spike2 Software Into Matlab, supplied by MathWorks Inc, used in various techniques. Bioz Stars score: 98/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/computer+software+utilities+2019b/pmc08051693-105-12-15?v=MathWorks+Inc
Average 98 stars, based on 1 article reviews
spike2 software into matlab - by Bioz Stars, 2026-08
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Image Search Results


Augmented antibody titer, viral neutralization, and lymph node retention of RBD-bann protein vaccine. RBD variants were isolated from the supernatants of mammalian cells via affinity chromatography and analyzed for purity and specificity via SDS-PAGE ( a ) and the binding of recombinant proteins at a serial dilution, or buffer alone (0), to immobilized human ACE2 receptor was measured in an ELISA assay ( b ). Dissociation of RBD and RBD-bann from immobilized hACE2 was measured by SPR ( c ). Mice were immunized with RBD and RBD-bann proteins purified from mammalian cell supernatant with/without squalene-mediated adjuvant. End point titer (EPT) for total IgG against RBD ( d – e ) and against spike protein ( f – g ). Graphs represent the mean EPTs of groups of mice ( n = 6 per group). Each dot represents an individual animal. * p < 0.05; ** p < 0.01. All p values are from the Mann–Whitney test compared to RBD group + AddaVax. Neutralization titer in mice sera was determined using a pseudovirus system. Sera of mice immunized with isolated proteins were diluted 50-fold, and Spike-pseudotyped virus infection of ACE2 and TMPRSS2-transfected HEK293 cells was followed by luminescence. Mean and SEM biological replicates are shown ( b ). * p < 0.05, *** p < 0.001, **** p < 0.0001. All p values are from one-way ANOVA followed by Tukey’s multiple comparisons test compared to the buffer group ( h ). A serum virus neutralization assay was performed by infecting Vero E6 cells with SARS-CoV-2-GFP reporter virus (MOI 1) with prior incubation of inoculum with dilutions of mouse sera (1:50) immunized with indicated isolated proteins. As control cells were left uninfected (mock), GFP signal was measured 36-h post-infection using the Incucyte S3 live-cell imaging system. Each point represents the mean of two technical replicates, and the mean +/− SD from six mice per group is indicated. Indicated p -values apply for comparison between individual conditions and the dilution-matched buffer condition and were calculated using a one-sided Student’s t -test between RBD + Addaax and RBD-bann + Addavax. * p < 0.05 ( i ). Trafficking of labeled isolated proteins into the popliteal lymph nodes (PLN). AF-647 labeled RBD proteins were injected into the foot pad (RBD left, RBD-bann right). The fluorescence signal of AF-647 was determined in the popliteal lymph node, depicting the presence of labeled RBD. Each dot represents the measurement of the region of interest (ROI) of an individual animal PLN. * p < 0.05 derived from two-tailed paired t -test ( j ).

Journal: Vaccines

Article Title: A Nanoscaffolded Spike-RBD Vaccine Provides Protection against SARS-CoV-2 with Minimal Anti-Scaffold Response

doi: 10.3390/vaccines9050431

Figure Lengend Snippet: Augmented antibody titer, viral neutralization, and lymph node retention of RBD-bann protein vaccine. RBD variants were isolated from the supernatants of mammalian cells via affinity chromatography and analyzed for purity and specificity via SDS-PAGE ( a ) and the binding of recombinant proteins at a serial dilution, or buffer alone (0), to immobilized human ACE2 receptor was measured in an ELISA assay ( b ). Dissociation of RBD and RBD-bann from immobilized hACE2 was measured by SPR ( c ). Mice were immunized with RBD and RBD-bann proteins purified from mammalian cell supernatant with/without squalene-mediated adjuvant. End point titer (EPT) for total IgG against RBD ( d – e ) and against spike protein ( f – g ). Graphs represent the mean EPTs of groups of mice ( n = 6 per group). Each dot represents an individual animal. * p < 0.05; ** p < 0.01. All p values are from the Mann–Whitney test compared to RBD group + AddaVax. Neutralization titer in mice sera was determined using a pseudovirus system. Sera of mice immunized with isolated proteins were diluted 50-fold, and Spike-pseudotyped virus infection of ACE2 and TMPRSS2-transfected HEK293 cells was followed by luminescence. Mean and SEM biological replicates are shown ( b ). * p < 0.05, *** p < 0.001, **** p < 0.0001. All p values are from one-way ANOVA followed by Tukey’s multiple comparisons test compared to the buffer group ( h ). A serum virus neutralization assay was performed by infecting Vero E6 cells with SARS-CoV-2-GFP reporter virus (MOI 1) with prior incubation of inoculum with dilutions of mouse sera (1:50) immunized with indicated isolated proteins. As control cells were left uninfected (mock), GFP signal was measured 36-h post-infection using the Incucyte S3 live-cell imaging system. Each point represents the mean of two technical replicates, and the mean +/− SD from six mice per group is indicated. Indicated p -values apply for comparison between individual conditions and the dilution-matched buffer condition and were calculated using a one-sided Student’s t -test between RBD + Addaax and RBD-bann + Addavax. * p < 0.05 ( i ). Trafficking of labeled isolated proteins into the popliteal lymph nodes (PLN). AF-647 labeled RBD proteins were injected into the foot pad (RBD left, RBD-bann right). The fluorescence signal of AF-647 was determined in the popliteal lymph node, depicting the presence of labeled RBD. Each dot represents the measurement of the region of interest (ROI) of an individual animal PLN. * p < 0.05 derived from two-tailed paired t -test ( j ).

Article Snippet: The normalized GFP intensity was computed using the IncuCyte S3 software (Essen Bioscience; version 2019B Rev2, Sartorius, Göttingen, Germany) as integrated GFP intensity per well divided by the total area of the cells per well.

Techniques: Neutralization, Isolation, Affinity Chromatography, SDS Page, Binding Assay, Recombinant, Serial Dilution, Enzyme-linked Immunosorbent Assay, Purification, Adjuvant, MANN-WHITNEY, Virus, Infection, Transfection, Incubation, Control, Live Cell Imaging, Comparison, Labeling, Injection, Fluorescence, Derivative Assay, Two Tailed Test

Heatmaps showing differences in macular retinal nerve fiber layer (mRNFL). Left map: this heatmap represents simple differences of mean thickness between OHT group and early POAG group in each superpixel giving an idea of the trend. Right map: the heatmap represents statistically significant differences ( p < 0.05) of the mean thickness between groups in each superpixel. No significant difference ( p ≥ 0.05) is represented in black. Range of significant OHT-POAG differences in superpixels between −20.70 and −1.35 microns.

Journal: Journal of Clinical Medicine

Article Title: Glaucomatous Maculopathy: Thickness Differences on Inner and Outer Macular Layers between Ocular Hypertension and Early Primary Open-Angle Glaucoma Using 8 × 8 Posterior Pole Algorithm of SD-OCT

doi: 10.3390/jcm9051503

Figure Lengend Snippet: Heatmaps showing differences in macular retinal nerve fiber layer (mRNFL). Left map: this heatmap represents simple differences of mean thickness between OHT group and early POAG group in each superpixel giving an idea of the trend. Right map: the heatmap represents statistically significant differences ( p < 0.05) of the mean thickness between groups in each superpixel. No significant difference ( p ≥ 0.05) is represented in black. Range of significant OHT-POAG differences in superpixels between −20.70 and −1.35 microns.

Article Snippet: The differences of mean thickness in each superpixel between OHT and early POAG groups were represented using heatmaps (OriginPro 2019 b software, Origin Lab, Northampton, USA).

Techniques:

Heatmaps showing differences in ganglion cell layer (GCL). Left map: this heatmap represents simple differences of mean thickness between OHT group and early POAG group in each superpixel, giving an idea of the trend. Right map: the heatmap represents statistically significant differences ( p < 0.05) of the mean thickness between groups in each superpixel. No significant difference ( p ≥ 0.05) is represented in black. Range of significant OHT-POAG differences in superpixels between −6.85 and −1.35 microns.

Journal: Journal of Clinical Medicine

Article Title: Glaucomatous Maculopathy: Thickness Differences on Inner and Outer Macular Layers between Ocular Hypertension and Early Primary Open-Angle Glaucoma Using 8 × 8 Posterior Pole Algorithm of SD-OCT

doi: 10.3390/jcm9051503

Figure Lengend Snippet: Heatmaps showing differences in ganglion cell layer (GCL). Left map: this heatmap represents simple differences of mean thickness between OHT group and early POAG group in each superpixel, giving an idea of the trend. Right map: the heatmap represents statistically significant differences ( p < 0.05) of the mean thickness between groups in each superpixel. No significant difference ( p ≥ 0.05) is represented in black. Range of significant OHT-POAG differences in superpixels between −6.85 and −1.35 microns.

Article Snippet: The differences of mean thickness in each superpixel between OHT and early POAG groups were represented using heatmaps (OriginPro 2019 b software, Origin Lab, Northampton, USA).

Techniques:

Heatmaps showing differences in inner plexiform layer (IPL). Left map: this heatmap represents simple differences of mean thickness between OHT group and early POAG group in each superpixel giving an idea of the trend. Right map: the heatmap represents statistically significant differences ( p < 0.05) of the mean thickness between groups in each superpixel. No significant difference ( p ≥ 0.05) is represented in black. Range of significant OHT-POAG differences in superpixels between −3.36 and −1.22 microns.

Journal: Journal of Clinical Medicine

Article Title: Glaucomatous Maculopathy: Thickness Differences on Inner and Outer Macular Layers between Ocular Hypertension and Early Primary Open-Angle Glaucoma Using 8 × 8 Posterior Pole Algorithm of SD-OCT

doi: 10.3390/jcm9051503

Figure Lengend Snippet: Heatmaps showing differences in inner plexiform layer (IPL). Left map: this heatmap represents simple differences of mean thickness between OHT group and early POAG group in each superpixel giving an idea of the trend. Right map: the heatmap represents statistically significant differences ( p < 0.05) of the mean thickness between groups in each superpixel. No significant difference ( p ≥ 0.05) is represented in black. Range of significant OHT-POAG differences in superpixels between −3.36 and −1.22 microns.

Article Snippet: The differences of mean thickness in each superpixel between OHT and early POAG groups were represented using heatmaps (OriginPro 2019 b software, Origin Lab, Northampton, USA).

Techniques:

Heatmaps showing differences in inner nuclear layer (INL). Left map: this heatmap represents simple differences of mean thickness between OHT group and early POAG group in each superpixel giving an idea of the trend. Right map: the heatmap represents statistically significant differences ( p < 0.05) of the mean thickness between groups in each superpixel. No significant difference ( p ≥ 0.05) is represented in black. Range of significant OHT-POAG differences in superpixels between 1.33 and 2.52 microns.

Journal: Journal of Clinical Medicine

Article Title: Glaucomatous Maculopathy: Thickness Differences on Inner and Outer Macular Layers between Ocular Hypertension and Early Primary Open-Angle Glaucoma Using 8 × 8 Posterior Pole Algorithm of SD-OCT

doi: 10.3390/jcm9051503

Figure Lengend Snippet: Heatmaps showing differences in inner nuclear layer (INL). Left map: this heatmap represents simple differences of mean thickness between OHT group and early POAG group in each superpixel giving an idea of the trend. Right map: the heatmap represents statistically significant differences ( p < 0.05) of the mean thickness between groups in each superpixel. No significant difference ( p ≥ 0.05) is represented in black. Range of significant OHT-POAG differences in superpixels between 1.33 and 2.52 microns.

Article Snippet: The differences of mean thickness in each superpixel between OHT and early POAG groups were represented using heatmaps (OriginPro 2019 b software, Origin Lab, Northampton, USA).

Techniques:

Heatmaps showing differences in outer plexiform and outer nuclear segmentation (OPLONL). Left map: this heatmap represents simple differences of mean thickness between OHT group and early POAG group in each superpixel giving an idea of the trend. Right map: the heatmap represents statistically significant differences ( p < 0.05) of the mean thickness between the groups in each superpixel. No significant difference ( p ≥ 0.05) is represented in black. The range of significant OHT-POAG differences in superpixels is between 2.68 and 5.66 microns.

Journal: Journal of Clinical Medicine

Article Title: Glaucomatous Maculopathy: Thickness Differences on Inner and Outer Macular Layers between Ocular Hypertension and Early Primary Open-Angle Glaucoma Using 8 × 8 Posterior Pole Algorithm of SD-OCT

doi: 10.3390/jcm9051503

Figure Lengend Snippet: Heatmaps showing differences in outer plexiform and outer nuclear segmentation (OPLONL). Left map: this heatmap represents simple differences of mean thickness between OHT group and early POAG group in each superpixel giving an idea of the trend. Right map: the heatmap represents statistically significant differences ( p < 0.05) of the mean thickness between the groups in each superpixel. No significant difference ( p ≥ 0.05) is represented in black. The range of significant OHT-POAG differences in superpixels is between 2.68 and 5.66 microns.

Article Snippet: The differences of mean thickness in each superpixel between OHT and early POAG groups were represented using heatmaps (OriginPro 2019 b software, Origin Lab, Northampton, USA).

Techniques:

Heatmaps showing differences in photoreceptor layer. Left map: this heatmap represents simple differences in the mean thickness between the OHT group and early POAG group in each superpixel, giving an idea of the trend. Right map: the heatmap represents the statistically significant differences ( p < 0.05) of the mean thickness between groups in each superpixel. No significant difference ( p ≥ 0.05) is represented in black. Range of significant OHT-POAG differences in superpixels between 1.08 and 2.63 microns.

Journal: Journal of Clinical Medicine

Article Title: Glaucomatous Maculopathy: Thickness Differences on Inner and Outer Macular Layers between Ocular Hypertension and Early Primary Open-Angle Glaucoma Using 8 × 8 Posterior Pole Algorithm of SD-OCT

doi: 10.3390/jcm9051503

Figure Lengend Snippet: Heatmaps showing differences in photoreceptor layer. Left map: this heatmap represents simple differences in the mean thickness between the OHT group and early POAG group in each superpixel, giving an idea of the trend. Right map: the heatmap represents the statistically significant differences ( p < 0.05) of the mean thickness between groups in each superpixel. No significant difference ( p ≥ 0.05) is represented in black. Range of significant OHT-POAG differences in superpixels between 1.08 and 2.63 microns.

Article Snippet: The differences of mean thickness in each superpixel between OHT and early POAG groups were represented using heatmaps (OriginPro 2019 b software, Origin Lab, Northampton, USA).

Techniques:

Heatmaps showing differences in the retinal pigment epithelium layer. Left map: this heatmap represents simple differences of mean thickness between OHT group and early POAG group in each superpixel giving an idea of the trend. Right map: the heatmap represents statistically significant differences ( p < 0.05) of the mean thickness between groups in each superpixel. No significant difference ( p ≥ 0.05) is represented in black. Range of significant OHT-POAG differences in superpixels between 0.51 and 0.75 microns.

Journal: Journal of Clinical Medicine

Article Title: Glaucomatous Maculopathy: Thickness Differences on Inner and Outer Macular Layers between Ocular Hypertension and Early Primary Open-Angle Glaucoma Using 8 × 8 Posterior Pole Algorithm of SD-OCT

doi: 10.3390/jcm9051503

Figure Lengend Snippet: Heatmaps showing differences in the retinal pigment epithelium layer. Left map: this heatmap represents simple differences of mean thickness between OHT group and early POAG group in each superpixel giving an idea of the trend. Right map: the heatmap represents statistically significant differences ( p < 0.05) of the mean thickness between groups in each superpixel. No significant difference ( p ≥ 0.05) is represented in black. Range of significant OHT-POAG differences in superpixels between 0.51 and 0.75 microns.

Article Snippet: The differences of mean thickness in each superpixel between OHT and early POAG groups were represented using heatmaps (OriginPro 2019 b software, Origin Lab, Northampton, USA).

Techniques: