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Jmp software version 11

Manufactured by SAS Institute
Sourced in United States, Japan

JMP software version 11 is a data analysis and visualization tool developed by SAS Institute. It provides a range of statistical and analytical capabilities for users to explore, analyze, and understand their data. The software offers features for data management, modeling, and reporting, enabling users to gain insights and make informed decisions.

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88 protocols using jmp software version 11

1

Statistical Analysis of Research Ratios

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The High prominence:Low prominence ratio and the High frequency:Low frequency ratio were calculated similarly to the Serious:Non-serious ratio described above.
JMP software version 11.1.1 (SAS institute, Cary, North Carolina, USA) was used for the analysis.
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2

Statistical Analysis of Continuous and Categorical Variables

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Statistical analysis was performed using JMP software version 11.1.1 (SAS Institute Inc., Cary, NC, USA). Results are summarized as medians and ranges for continuous variables, and categorical variables are summarized as numbers. The median values were compared between groups using the Mann-Whitney test or the chi-square test in univariate analysis. Statistical significance was defined as p<0.05.
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3

Statistical Analysis of Clinical Variables

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Statistical analysis was performed using the JMP software, version 11.0 (SAS). Normally distributed data are expressed as mean ± standard deviation and non‐normally distributed data as median and interquartile range. Univariate analyses of various clinical variables were performed using unpaired t‐tests for normally distributed data, and Wilcoxon's rank sum test for non‐normally distributed data. Fisher's exact test was used for categorical data.
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4

Comparative Analysis of Visual Outcomes

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The data obtained from all patients were analyzed with frequency and descriptive statistics. The logMAR BCVA and the mean measurement values were compared using the Mann–Whitney U test. Categorical data were tested using Fisher’s exact test. A P-value <0.05 was considered significant. All descriptive statistics were performed using JMP software version 11.0 (SAS Institute Inc., Cary, NC, USA).
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5

Statistical Analysis of Medical Data

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Statistical analysis was performed using the Mann-Whitney U-test to compare median values and Fisher’s exact test to compare frequencies. Receiver operating characteristic (ROC) curve analysis was used to determine the most suitable cut-off level. A value of P <0.05 indicated statistical significance. The data were analyzed using JMP software, version 11.0 (SAS Institute, Cary, NC, USA).
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6

Comparison of Hypersensitivity Reaction and Survival

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Pearson’s chi-test was used for categorical variables. The Kaplan–Meier method was used to estimate the cumulative incidence of hypersensitivity reaction, the median PFS, and OS curves for each treatment arm. Comparisons between the intergroup were performed using two-sided log-rank and Wilcoxon square tests. PFS was defined as the interval between the administration of cisplatin and progressive disease or death. OS was defined as the interval between cisplatin administration and death. All data were analyzed based on the intention-to-treat principle. All tests were two-sided. A p-value of <0.05 was considered statistically significant. All analyses were performed using JMP software, version 11.0 (SAS, Cary, NC, USA).
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7

Bacterial Adhesion Assay and Growth Dynamics

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Adhesion indexes of bacterial strains to intestinal cells were compared among treatments using the one-way analysis of variance (ANOVA) general linear model followed by Tukey’s HSD test. L. monocytogenes counts in Macfarlane broth in the absence or presence of E. faecium were compared using MANOVA for repeated measures (time as repeated measures variable) followed by Tukey’s HSD test. Statistical significance was declared at P < 0.05. All statistical analyses were performed using JMP® software version 11.0 (SAS Institute Inc., Cary, NC, United States).
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8

Factors Associated with Intravenous Medication Needs During TELD

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Multivariate regression analysis was performed to identify factors associated with the need for additional intravenous medication due to pain or development of hypertension, hypotension, tachycardia, or bradycardia during the operation. The primary objective was the frequency of administration of additional intravenous medication during TELD. The explanatory variables were sex, age, body mass index, intervertebral disc level, distance between the superior articular process and the exiting nerve root (measured on axial MRI), height of the intervertebral disc, height of the bulging disc, height of the intervertebral foramen (measured on CT images), and distance from the insertion site to the spinous process. JMP software version 11.0 (SAS Institute Inc., Cary, NC, USA) was used for the statistical analysis.
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9

Polynomial Modeling and Statistical Analysis

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The second-order polynomial models and the three-dimensional (3D) surface and two-dimensional (2D) contour plots for the process yield and the retentions of TSC, TPC, TFC and TAA were generated using the JMP software version 11.0 (SAS Institute Inc., Cary, NC, USA). The adequacy of the models was determined based on the coefficient of determination (R2) and the lack of fit. Results were expressed as mean values with standard deviations. Significant differences between means were determined by analysis of variance (ANOVA), the Bonferroni post-hoc test and the 5% significance level (p < 0.05) using the SPSS software version 19.0 (IBM Australia Limited, St. Leonard, NSW, Australia). Pearson correlation coefficients were also determined using the SPSS software.
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10

LGR5-Positive Tumor Cell Analysis

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Statistical analyses were performed using JMP software version 11.0 (SAS Institute, Cary, NC, USA). Possible differences between groups were analysed using Student's t-test or Mann–Whitney U-test appropriately. The population of LGR5 exon 5-positive cells was their ratio among all tumour cells in 50 HPF. A probability level of 0.05 was chosen to indicate significance.
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