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139 protocols using jmp 7

1

Glomerular Immune Complex Analysis

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All values were examined by mean ± SD. Differences between the two groups were evaluated using a Mann-Whitney’s U test. Comparisons among three or more parameters were analyzed by analysis of variance. P < 0.05 was defined as statistical significant. Statistical analyses, including contour plots, in which data from pIgA1 trap form the X-axis, data from ELISA form the Y axis, and other clinical parameters form a pseudo-Z axis via colors (age, interval between onset and biopsy, Area-IgA, Area-IgG, Area-C3, serum IgA, serum C3, the IgA/C3 ratio, s-Cr, eGFR, and urinary protein excretion), were performed using JMP7 (SAS Institute, Cary, NC, USA).
To verify Area-IgA in glomerulus, a decision tree analysis was used with the HAA ELISA titer and pIgA1 trap value by JMP7. Decision tree algorithms aim to divide the data set into subsets that give the best discrimination between groups. Each subset (called a node in a decision tree) can split the data set into subsets to sharpen the discrimination between groups. A 10-fold cross validation was performed by WEKA (Waikato Environment for Knowledge Analysis).
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2

Turbidimetric Titration Data Analysis

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The turbidity data from the turbidimetric titrations were analyzed by one-way analysis of variance (ANOVA) with a 95% confidence interval (α = 0.05) and Tukey’s HSD test. Statistical analysis of the data was carried out with the SAS software JMP 7.0.2.
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3

Evaluation of Treatment Efficacy

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All experimental data were presented as mean ± standard deviation. Data were analysed using JMP 7.0.2 (SAS Institute Inc., Cary, NC, USA). One-way analysis of variance and the post-hoc Tukey's honest significant difference test were used to evaluate differences between groups. P<0.05 was considered to indicate a statistically significant difference.
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4

Comparative Statistical Analysis of Experimental Data

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All experimental data were presented as the mean±standard error of the mean: data were analyzed using the JMP 7.0.2 program (SAS Institute Inc., SAS Campus Drive, Cary, NC, USA 27513). One-way analysis of variance (ANOVA) and the post hoc Tukey HSD test were used to evaluate differences between groups: *P<0.05, #P<0.05 were considered significant.
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5

Floral Morphology Variation in Solanum rostratum

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In order to characterize the variation in floral morphology among natural populations of S. rostratum, we collected floral morphology data from six populations across a latitudinal gradient in Mexico during October and November of 2010 (Table 1). In each population, we measured between two and four flowers from 16 to 30 individuals (Table 1). For each flower, we measured the following ten traits with digital calipers: corolla length (1) and width (2); the length of the anther and the width of the anther at its widest point, for both the feeding (3, 4) and pollinating anther (5, 6); the length of the style (7); the distances between: the stigma and the pollinating anther (8), the stigma and the nearest feeding anther (9) and the pollinating anther and the nearest feeding anther (10; Figure 1). We analyzed these floral measurements using principal component analysis (PCA) of a correlation matrix. Differences among populations in the first two principal components were analyzed using an analysis of variances (ANOVA) of the principal component scores, and a Tukey post hoc test. For this analysis, we used JMP 7.0.2 (SAS Institute Inc. 2007) and plotted the results with Sigmaplot 13 (Systat Software Inc. 2015).
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6

α-Glucosidase Inhibitor Activity Evaluation

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Data are presented as the means ± standard deviation (SD) for in vitro experiments and as the means ± standard error of the mean (SEM) for in vivo experiments. Statistical analysis were performed by JMP 7.0.2 (SAS Institute Inc., Cary, NC, USA). The significance analysis of differences in inhibitory activity among α-glucosidase inhibitors was conducted by an unpaired Student's t-test (p < 0.05), and the blood glucose level of each group was ascertained by a Tukey–Kramer HSD test (p < 0.05).
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7

Seasonal Variations in Fish Blood Chemistry

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Statistical analyses were performed separately for each fish species, with a focus on intraspecific differences in blood chemistry values between seasons. Blood-based metrics were normally distributed and compared using a two-way analysis of variance (ANOVA) with treatment and season as main effects, and treatment × season as an interaction term. Tukey's post hoc test was performed when at least one main effect or the interaction term was deemed significantly different. Data analysis was completed using JMP 7.0.2 (SAS Institute, Cary, NC, USA) with α = 0.05.
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8

Antibody Levels and Infection Correlation

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Group comparisons were performed using a one-way analysis of variance (ANOVA) and Student's t-test. Significant levels were set at P < 0.05. Group data are expressed as means ± S.D. Correlation of infection levels and mucus antibody in individual fish was performed using Kendall's τ. All calculations were performed using the statistical software JMP-7.0.2 (SAS Institute, 2007; Cary, NC).
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9

Arteriovenous Fistula Patency Analysis

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The patency rate was estimated using the Kaplan–Meier technique. The difference in the patency rate between the two groups was examined using a log-rank test. A univariate analysis of categorical variables was made with a Chi squared test and a multivariate analysis of AVF survival was examined by the Cox proportional-hazards model. Data were expressed as mean ± standard deviation (M ± SD). p < 0.05 was considered significant. All statistical analyses were performed using the Windows version of JMP 7.0.2 software (SAS Institute Inc., Cary, NC, USA).
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10

Hierarchical Clustering of Rice Accessions

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Rice accessions were classified based on marker data and reactions to the SDBIs using Ward’s hierarchical clustering method with the computer program JMP7.0.2 (SAS Institute, Inc., Cary, NC, USA).
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