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Statistica software version 13

Manufactured by StatSoft
Sourced in Poland, United States, Germany

Statistica software version 13.3 is a data analysis and statistical software package developed by StatSoft. It provides a comprehensive set of tools for data management, visualization, and advanced statistical analysis.

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91 protocols using statistica software version 13

1

Analyzing Aflatoxin Accumulation in Corn Hybrids

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All statistical tests used in the analysis belong to the group of non-parametric tests that do not assume the shape of data distribution. Spearman’s rank correlation tests were used for correlation analyses between Aspergillus ear rot, aflatoxin B1 accumulation, and grain yield. Friedman test was performed to determine differences in aflatoxin production of 20 hybrids according to the test period. Wilcoxon signed rank test was used to determine differences between hybrids according to the sowing dates. All statistical analyses were carried out using STATISTICA software, version 13 (StatSoft Inc., Tulsa, OK, USA).
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2

Gender Differences in Physical Fitness

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The t-test was used to evaluate gender differences in the results obtained during physical fitness test. For the comparison of the time spent on sedentary behavior and frequency of undertaking of different forms of PA according to gender, Mann–Whitney U test was used. The differences between genders in prevalence of underweight, normal weight and overweight were assessed based on percentage values using the test for difference between two independent sample proportions. Statistical significance was set at a probability of p < 0.05. Data were analyzed using STATISTICA software, version 13 (StatSoft Polska, Krakow, Poland).
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3

Assessing Apheresis Session Effects

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Statistical analyses were performed using the STATISTICA software version 13 (StatSoft, Kraków, Poland). The Shapiro–Wilk test was used to test the normality of the distribution of variables. The variables are expressed as medians with the 25th and 75th percentiles. Friedman's test (p = 0.002) with Dunn's test as a post hoc test was used to assess the changes in individual parameters because of apheresis sessions. Univariate correlations were assessed using standardized Spearman coefficients. P values below 0.05 were considered statistically significant.
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4

Statistical Analysis of Biological Data

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Results are given either as means ± SEM of the original values or as means of % of control±SEM. Results exceeding + /−2SDs were excluded. Statistical analysis was carried out either by two-way ANOVA or by repeated measures ANOVA as appropriate and indicated for each analysis, followed by post-hoc Fisher’s Least Significant Difference (LSD) test, using STATISTICA software version 13 (StatSoft, Tulsa, Oklahoma). The data met the assumptions of the tests, namely, normal distribution and the variance between the compared groups was similar. p ≤ 0.05 was considered statistically significant. As a rule of thumb, according to our years of experience, and as can be found in others’ recent reports in a high impact journal [52 (link), 53 (link)] a minimal number of animals or samples/group to achieve reproducibility is 5.
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5

Fitness Changes and Questionnaire Evaluation

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To assess the changes of fitness in the examined groups in relation to the examination terms, the analysis of variance (ANOVA) test was used with Tukey’s post hoc test. To compare the results of the questionnaire items in three examination terms, Friedman’s ANOVA test was used with post-hoc analysis between the terms. For testing the differences between the medians in the groups of boys and separately between the groups of girls in all three terms, the Mann–Whitney U test was used for the questionnaire items. The statistical significance was set at p < 0.05. Analyses were carried out with the use of STATISTICA software, version 13 (StatSoft, Krakow, Poland).
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6

Normalization and Intergroup Comparisons

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Data was tested for normality and for baseline differences between groups. Plasma NGAL, heart rate, plasma lactate, and WBC data were log-transformed to achieve normal distribution. Intergroup differences were assessed with repeated measures ANOVA type III for normally distributed data. If group difference was found, a post hoc test with unequal N test for groups Etx + NaCl vs. Hct + Etx, groups Etx + NaCl vs. Etx + Hct, and groups Etx + Hct vs. Hct + Etx was performed. Intergroup differences were assessed for non-normally distributed data with Kruskal-Wallis test. Change over time, for non-normally distributed data, was assessed with Friedman’s ANOVA. A Spearman Rank Order test was performed to analyze correlation between data. p < 0.05 was considered significant. We report values as means with standard deviation (SD) or medians with interquartile ranges (IQRs) when appropriate. Analyses were performed by using STATISTICA software, version 13 (StatSoft, Tulsa, OK).
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7

Amino Acid Analysis of WML-P

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All experiments were performed in triplicate and the results are mean ± SD. The amino acid content of WML-P analysis was performed in duplicate. Data were analyzed using one-way analysis of variance (ANOVA), followed by Tukey’s post-hoc test. Statistical differences were calculated at the significance level p < 0.05 and represented by superscript letters. The statistical analysis was performed using Statistica software, version 13 (StatSoft, Kraków, Poland).
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8

Statistical Analysis of Experimental Outcomes

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Statistical analyses were carried out using STATISTICA software, version 13 (StatSoft, Tulsa, OH, USA). P-values < 0.05 were considered statistically significant. Variables are presented as mean ± SEM. Normality of variables was tested using the Kolmogorov–Smirnov and Lilliefors tests. Differences between 2 dependent values were tested using Wilcoxon Matched Pair test. Differences between 2 groups were tested using Mann-Whiney test. Differences between the three groups’ variables were tested using Kruskal–Wallis ANOVA and Median test. Differences within each group over the 2 years were tested using Friedman ANOVA. Correlations were tested using Spearman Rank Order Correlation. Logistic regressions were preformed to test which parameters affected primary outcome.
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9

Pollution Source Apportionment using PMF

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Statistical analysis was performed using the STATISTICA software version 13 (StatSoft Europe GmbH, Hamburg, Germany). For the analysis of the results variance, non-parametric statistics at a significance level of 0.050 were selected. Mann-Whitney tests were used to assess significant differences between datasets.
The Positive Matrix Factorization (PMF) model was used to identify the pollution sources contributing to PM levels [25 ]. PMF is a popular receptor model used for source apportionment studies, which decomposes the data matrix into two sub-data matrixes (factor profiles and factor contributions) without prior knowledge of the profiles of pollution sources [26 (link)]. PMF was applied to the datasets of PM sampled in “Quebedo” and “Mitrena”. Data below the limit of detection (LoD) were replaced by LoD/2 and the uncertainties were set to 5/6 of the LoD.
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10

Fatty Acid Analysis in Inflammatory Bowel Disease

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Descriptive statistics (mean values, SD, medians, quartiles Q1-Q3) were used in the statistical assessment of the results. Statistica software version 13 (StatSoft) was used to perform statistical analysis. To evaluate the distribution of continuous variables in terms of their compliance with the normal distribution, the Shapiro-Wilk test was employed. Student’s t-test was applied to compare the mean value of fatty acids for normally distributed continuous variables. In the case of non-normal distribution, the Mann-Whitney U test was used. Pearson’s correlation was used to examine relationships between the Geboes activity index and the level of fatty acids. A p-value less than 0.05 was considered statistically significant.
The study was conducted according to the guidelines of the Declaration of Helsinki and approved by the Jagiellonian University Ethics Committee (decision no. KBET/35/B/2014).
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