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Spss program for windows

Manufactured by IBM
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SPSS is a software program designed for statistical analysis and data management. It is a comprehensive analytical tool that enables users to efficiently organize, analyze, and interpret a wide range of data. SPSS provides a user-friendly interface and a wide range of statistical techniques, allowing researchers, analysts, and decision-makers to extract meaningful insights from their data.

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42 protocols using spss program for windows

1

Sample Size Calculation for Exploratory Analysis

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For calculation of the study sample size, we used a priori G*power analysis (Faul, Erdfelder, Lang, Buchner, 2007, version 3, University of Dusseldorf, Germany) based on α (type I error) = 0.05 and β (type II error) = 0.2 (power = 80%). Thirty-eight patients per group were sufficient to find a difference of 25% in the incidence of EA between them. There was a predicted 5% dropout of cases, so 40 subjects were required in each group to detect such difference.
Analysis of the collected data was performed using the SPSS program for Windows (version 26, IBM Corp, Armonk, New York, USA). At first, data normality was checked using the Kolmogorov–Smirnov test. Qualitative or categorical variables were presented as numbers and percentages to be compared using the Chi-square test or Fisher's exact test. Continuous variables were expressed as mean ± standard deviation if normally distributed, and median (range) for nonnormal data. Both the groups were compared parametrically using Student's t-test, and nonparametrically with MannWhitney U-test. All data were considered statistically significant if P ≤ 0.05, where more significant results were obtained with smaller P values.
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2

Rumination Behavior in Dairy Cows

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Statistical data processing was carried out in the SPSS program for Windows (version 26.0; IBM Corp. Armonk, New York, NY) with normally distributed variables (according to the Kolmogorov–Smirnov test and graphical methods of histograms and Q-Q plots) of rumination behavior in cows.
Considering the design of the study, we divided the data of cows into three stages for statistical evaluation: (1) the last thirty days before calving (from day −30 to −1 of the study); (2) day of calving (this day was excluded due to the possible influence of the calving process); (3) the first thirty days after calving (from day 1 to 30 of the study).
The significance of the differences between the mean values of two independent groups was assessed using the independent samples t-test. Student’s test for dependent samples was used to compare sample means from two periods of the experiment for the same groups.
Correlation analysis of indicators of ruminant behavior of individual cows before and after calving was carried out with the calculation of the Pearson correlation.
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3

Evaluating Postoperative Emergence Delirium

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The sample size (58 patients per group) was determined using the GPower software, based on a study by Chandler et al,8 (link) to detect a reduction of >50% (from 38.3% to 14.9%) in ED with a power of 80% using a Student’s t-test to compare means with an alpha value of 0.05.
The SPSS program for Windows (Version 20.0; IBM Corporation, Armonk, NY, USA) was used for the statistical analysis. All data were subjected to the Kolmogorov–Smirnov test for normality. Two sample t-tests were used to compare age, weight, duration of the operation, duration of anesthesia, number of dental procedure types, recovery time, extubation time, and guardians’ satisfaction levels between the two groups. Chi-square tests were used to compare the presence of ED between the two groups. The relationship between PAED and FLACC scores was investigated using Spearman’s rank correlation coefficient. A 5% type 1 error level was used to determine statistical significance.
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4

Nonparametric Analysis of NogoA Data

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Statistical analysis of non-normal distributed data generated by NogoA-immunohistochemistry was performed by using IBM “Statistic Package for Social Sciences” SPSS program for Windows (version 24) and applying a Mann-Withney U-test for two independent samples. A p-value of less than or equal to 0.05 was considered statistically significant.
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5

Effects of Vitamin D Supplementation

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All analyses were carried out using the Statistical Package for the Social Sciences (SPSS) program for Windows (version 20.0, released in 2011; IBM Corp. Armonk, New York, USA). The main characteristics of patients were evaluated with descriptive and analytical statistics. Categorical variables were compared by chi-square test. The mean values of the continuous variables were compared using the independent-samples or paired-samples Student's t-test as appropriate. The normal distribution of continuous variables was tested using a Kolmogorov-Smirnov test. Normally distributed paired data were analyzed with a paired t-test, whereas skewed paired data were analyzed using the Wilcoxon test. Data were expressed as mean±SD or median (minimummaximum). The Spearman correlation coefficient was used to evaluate the correlation between the improvement in 25(OH) D and the NCS. P-values<0.05 were considered to be statistically significant.
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6

ANOVA Analysis of Experimental Data

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Data were analyzed using the analysis of variance (ANOVA) by using SPSS program for windows (Version 21) (SPSS, IBM Corporation, Armonk, New York, USA). The multiple range least significant difference test L.S.D. and Duncan multiple range tests were applied to the results (P< 0.05) [35] (link).
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7

Normality Testing and Statistical Analysis

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Data are presented as mean values ± SD. For cell experiments, a Kolmogorov–Smirnov test was performed to test normality. Differences between groups were assessed by one-way ANOVA with Bonferroni correction or Kruskal–Wallis test depending on their distribution. SPSS program for Windows (Chicago, IL, USA) version 17.0 was used. Results were considered statistically significant at p values < 0.05.
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8

Genetic Polymorphisms Influence Outcomes

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Sample size was calculated by keeping the power 80%, and two-sided alpha error 0.05% minimum 64 patients were required to observe resistance pattern as per the previous assumption. Continuous variables are presented as mean ± standard deviation and categorical variables are presented as absolute numbers and percentage. The Fisher's exact test was used to determine the relationship between gene polymorphisms in different groups of patients and to determine the association of these gene variants with comorbidities and clinical outcome. P < 0.05 was considered statistically significant. All the statistical analysis was performed by the SPSS program for Windows (version 20, SPSS, version 20, Chicago, IL, USA).
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9

Statistical Analysis of Experimental Data

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The distribution of the data was evaluated using the Kolmogorov–Smirnov test. All of the data are expressed as the means ± S.D. of three independent experiments, each performed in triplicate. One-way ANOVA for repeated measures and Bonferroni post-hoc analyses were performed in order to determine significant variation among groups for each variable tested. A value of p < 0.05 was accepted as statistically significant. The SPSS program for Windows (Version 17.0; SPSS Inc., Chicago, IL, USA) was used for all statistical analyses. The analysis performed between untreated controls and control vehicles (CTRLm) showed no statistical differences for all variables tested (data not shown).
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10

Normality Testing and Statistical Analysis

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Data are presented as mean values ± SD. For cell experiments, a Kolmogorov–Smirnov test was performed to test normality. Differences between groups were assessed by one-way ANOVA with Bonferroni correction or Kruskal–Wallis test depending on their distribution. SPSS program for Windows (Chicago, IL, USA) version 17.0 was used. Results were considered statistically significant at p values < 0.05.
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