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Spss for macintosh version 25

Manufactured by IBM
Sourced in United States

SPSS for Macintosh, version 25.0 is a statistical software package developed by IBM. It provides tools for data analysis, including data manipulation, visualization, and statistical modeling.

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Lab products found in correlation

7 protocols using spss for macintosh version 25

1

Comparing Short-term and Long-term Strength Training

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All variables were normally distributed (Shapiro-Wilk test). Data are presented as means and standard deviation (SD). All statistical analyses were conducted using the statistical package SPSS for Macintosh (version 25.0, Chicago, IL, USA). A 2 (group: SST and LST) × 2 (time: pre, post) mixed factorial analysis of variance (ANOVA) was calculated for each parameter. Additionally, Cohen’s d was computed for comparing effect sizes (ES). ES were classified as trivial (d < 0.2), small (0.2 ≤ d < 0.5), moderate (0.5 ≤ d < 0.8), and large (≥ 0.8) [27 ]. Moreover, pre- to-post change percentage was calculated for corresponding variation. Relative and absolute reliability of the variables analyzed in this study were assessed using the intraclass correlation coefficient (ICC) and the coefficient of variation (CV), respectively. Significance was established at the P ≤ 0.05 level.
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2

Insulin Sensitivity and Lipid Profiling

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Lipids were divided into groups and analyzed based on carbon atom and double bond numbers. The typical cutoff value of GIR30 (or GDR, M value) of 4.9-5.2 mg/kg per minute was used to define insulin sensitive or resistant subjects (14, 19) . In our study, the cutoff point of GIR30 was set as 5.1 mg/(kg *min), which was also the median of consecutive 86 subjects. Differences in metabolic characteristics between two groups divided by GIR30 were calculated by t-test or the Mann-Whitney U test. Analyses were performed using SPSS for Macintosh version 25.0 (SPSS Inc, Chicago, IL, USA).
Associations between metabolic parameters and lipid species were analyzed by Pearson correlation based on univariate logistic regression and adjusted for multiple factors, including age, sex, BMI, HDLc, LDL-c, TG, TC, ALT and AST. Gephi was used to build correlation networks from differentially correlated lipid pairs. Data are presented as the mean ± SD or median (range). P<0.05 was considered statistically significant.
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3

Insulin Sensitivity and Lipid Profiling

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Lipids were divided into groups and analyzed based on carbon atom and double bond numbers. The typical cutoff value of GIR30 (or GDR, M value) of 4.9-5.2 mg/kg per minute was used to define insulin sensitive or resistant subjects (14, 19) . In our study, the cutoff point of GIR30 was set as 5.1 mg/(kg *min), which was also the median of consecutive 86 subjects. Differences in metabolic characteristics between two groups divided by GIR30 were calculated by t-test or the Mann-Whitney U test. Analyses were performed using SPSS for Macintosh version 25.0 (SPSS Inc, Chicago, IL, USA).
Associations between metabolic parameters and lipid species were analyzed by Pearson correlation based on univariate logistic regression and adjusted for multiple factors, including age, sex, BMI, HDLc, LDL-c, TG, TC, ALT and AST. Gephi was used to build correlation networks from differentially correlated lipid pairs. Data are presented as the mean ± SD or median (range). P<0.05 was considered statistically significant.
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4

Evaluating ANN for Hypospadias Diagnosis

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The sample size was estimated for a prespecified power of 90%, while the α value was set at <.05. The clinical characteristics of the participants and all hypospadias parameters will be presented descriptively. Intrarater and interrater analyses among pediatric urologists will be performed, using the Fleiss κ statistical analysis. The κ score between the ANN results and pediatric urologists’ examination results will be calculated by using SPSS for Macintosh, version 25.0 (IBM Corporation). The data will be deemed statistically significant if the P value is <.05. In addition, accuracy, precision, recall, and F1 score values will be computed to measure the performance of the recognition model.
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5

Logistic Regression for Primary Outcome

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All statistical analyses were performed using IBM SPSS for Macintosh, version 25.0 (Armonk, NY: IBM Corp). Continuous non-normal distributed variables were reported as median (IQR), with differences between the two groups assessed using the Mann-Whitney U-test and three groups using the Kruskal-Wallis test with a post-hoc Dunn-Bonferroni test. Dichotomous variables were presented as frequencies and percentages, with differences between groups assessed using the Chi-squared test. Associations of independent variables and the primary outcome were assessed through logistic regression and presented as odds ratios (ORs) with 95% CIs. Variables with statistically significant associations to the primary outcome on univariate logistic regressions were included in the multivariable logistic regression model. Before logistic regression, the variable of total serum IgE- concentrations was dichotomized and the patients allocated to either above or below maximum reference intervals according to age-specific cut-offs (Supplementary Table 1).
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6

Appendicitis Risk Stratification via HCC

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All statistical analyses were performed in IBM SPSS for Macintosh, version 25.0 (Armonk, NY: IBM Corp). Continuous non-normal distributed variables were reported as median (min–max), and differences between groups were assessed using the Mann–Whitney U-test. Dichotomous variables were presented as frequencies and percentages, and differences between groups were assessed using the Chi-squared test. The percentage difference in HCC between months 4–6 and 0–3 was calculated by dividing the value of HCC 4–6 months with the value of HCC 0–3 months. The values of HCC at month 0–3 and 4–6 were logarithmised before further analysis. The effect of HCC levels, at 0–3 months, 4–6 months, and the percentage difference in HCC, on (a) appendicitis and b) complicated appendicitis, were measured through univariate and multiple logistic regression and reported as odds ratios (OR) with 95% confidence intervals (95% CI). Independent variables included in the multiple regression analyses were age, sex, and any other significant (p < 0.05) variable from the univariate analyses.
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7

Vitamin D Status and Lung Function

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All data analyses were performed using Statistical Package for Social Science Statistics IBM SPSS for Macintosh, version 25.0 (IBM Corp., Armonk, N.Y., USA). Descriptive data are expressed as mean and standard deviation. Comparisons between the CF and non-CF control were conducted using the independent sample t-test. In the CF group, one-way analysis of variance (ANOVA) was used to assess differences in PFTs and gut microbiota composition across the three vitamin D subgroups (i.e., deficiency, insufficiency, and optimal). The correlations between 25(OH)D status and PFTs, or gut microbiota composition, and PFTs with gut microbiota composition were analyzed using the Pearson's correlation coefficient (two-tailed) test. A P-value <0.05 was considered significant in all tests.
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