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Statistics 21

Manufactured by IBM
Sourced in United States

Statistics 21.0 is a software package designed for statistical analysis and data modeling. It provides a comprehensive set of tools for data manipulation, visualization, and advanced statistical techniques. The core function of Statistics 21.0 is to enable users to perform a wide range of statistical analyses, from basic descriptive statistics to complex multivariate modeling, without extrapolating on its intended use.

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40 protocols using statistics 21

1

Seasonal DON Analysis Protocol

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The analysis of DON were statistically observed and represented as average levels and standard deviations. However, the samples below the detection limits, but greater than zero were substituted with LD2 , and the (R2) was analyzed using linear regression/correlation analysis. The significant difference in the levels of DON among different seasons was calculated using a one-way analysis of variance (SPSS, IBM, Statistics 21).
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2

Analyzing Treatment Effects Over Time

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Results were analyzed independently for each test. Poisson regression was employed to identify whether group has any significant difference over the time. To estimate the parameters of the model, we employed generalized estimating equations as over the time the responses are associated with employing R. To find the difference between placebo and treatment groups we checked normality assumption and employed statistical tests that appropriate. Repeated measure ANOVA was employed to observe between and within effect by using IBM Statistics 21. Repeated measure multivariate analysis was performed to find the effect of AS over four-week time period. Chi-square test was performed for demographic data between groups. p < 0.05 was considered statistically significant.
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3

Quantifying Endovascular Trophoblast Proximity

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Data are reported as means ± standard deviations. Student’s t-test was applied for the quantification of EVT replacing epi-/endothelium and EVT in spatial proximity between glands and vessels, after testing for normal distribution (Kolmogorov–Smirnov test). Statistical analysis was done using SPSS IBM Statistics 21. A P-value <0.05 was considered as significant.
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4

Quantitative Analysis of Cell Viability

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Data are presented as mean with SEM. Statistical analyses comparing treatment groups were performed using a one-way analysis of variance (ANOVA) with Bonferroni’s correction for multiple pairwise comparisons using IBM Statistics 21 (Armonk, NY, formerly SPSS), with P < 0.05 considered significant.
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5

Maternal Lactation Nutritional Dynamics

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Statistical analyses were performed using Statistica 12PL, Tulusa, USA and IBM Statistics 21, New York, NY, USA. A p-value below 0.05 was adopted as statistically significant. Variable distributions were evaluated with Shapiro–Wilk test, and descriptive statistics (means and standard deviations as well as medians and interquartile ranges) were calculated. The mothers’ anthropometric data and body composition, and the nutritional value of their diet in the first and sixth months of lactation were compared using a paired 2-sample Student’s t-test (normal distribution of differences between all pairs), or a Wilcoxon signed-rank test for paired samples (nonnormally distributed differences between all pairs). A trend analysis of milk composition at three time points was performed with the Jonckheere–Terpstra test, and its effect size was estimated with Kendall’s tau-b correlation coefficient. Correlations between milk composition and the mothers’ body composition and diet were estimated with Pearson’s r correlation coefficient.
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6

Human Milk Fatty Acid Analysis

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Statistical analyses were performed using Statistica 12PL, Tulusa, USA and IBM Statistics 21, New York, NY, USA. A p-value below 0.05 was adopted as statistically significant. Variables distributions were evaluated with a Shapiro–Wilk test and descriptive statistics. Data were presented as means and standard deviations as well as medians and interquartile ranges. Correlations between the intake of fatty acids and fatty acids concentrations in human milk were estimated with Pearson’s r correlation coefficient. Correlations between omega-3 fatty acids (DHA, EPA, ALA) concentrations in human milk, and food consumption frequency were estimated with Kendall’s tau correlation coefficients.
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7

Statistical Analysis of Experimental Data

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The data are presented as mean ± standard error of the mean (SEM), and it was considered significant when p < 0.05. Student’s t test or one-way ANOVA with post hoc test was used to analyse the data with intra- or intergroup. All statistical analyses were conducted using IBM Statistics 21 software (IBM, supplied by University of South Australia) or GraphPad Prism, Version 6.05 (GraphPad, supplied by University of South Australia; Graph Pad Inc., CA).
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8

Statistical Analysis of Experimental Treatments

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Data were analysed using one-way of variance, and treatment mean separations were performed using Duncan’s multiple range tests at the 5% level of significance in IBM Statistics 21.
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9

Assessing Alprazolam's Effects on Cognition

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Results were analyzed independently for each test. To find the difference between alprazolam and placebo group, we checked normality assumption and employed statistical tests that are appropriate. For each measure, performance under the drug condition was compared with that at baseline using a 2 (time; baseline, after two weeks) × 2 (treatment; placebo, alprazolam) mixed model ANOVA with repeated measures by using IBM Statistics 21 to find the effect of alprazolam over the period of two weeks. Chi-square test was performed for demographic data between groups. p < 0.05 was considered statistically significant.
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10

Apoplastic pH Profiling in Plant Roots

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Statistical tests were performed using IBM Statistics 21 (SPSS Inc., Chicago, IL, USA). Data-distribution normality was analyzed using the Shapiro-Wilk test. E 0 and η N were normalized via log-transformation. For pairwise comparisons, statistical differences were detected using a Student's t-test. For comparing apoplastic pH among the zones, cultivars, and treatments, the fluorescence intensity ratio (the intensity at 473 nm divided by the intensity at 405 nm) data were analyzed using a one-way ANOVA and Duncan's new multiple range test. To detect statistical differences between the groups, in terms of root segments, expansin expression, and pH, we used a three-way ANOVA with Bonferroni post-hoc tests. To compare expansin expression between the cultivars, we used Student's t-tests and Mann-Whitney tests.
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