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Spss for windows 13

Manufactured by IBM
Sourced in United States

SPSS for Windows 13.0 is a statistical software package designed to analyze and manipulate data. It provides a comprehensive set of tools for data management, analysis, and reporting.

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82 protocols using spss for windows 13

1

Statistical Analyses of Biological Data

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Statistical analyses were performed with SPSS for Windows 13.0. All continuous variable values were expressed as Mean ± SD (n = 3). Comparison of means between two groups was performed with student t tests. Comparisons of means among multiple groups were performed with one-way ANOVA followed by LSD test (homogeneity of variance) and Games—Howell test (heterogeneity of variance). P (probability) < 0.05 was accepted as statistically significant.
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2

Glycemic Factors and Coronary Heart Disease

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All statistical analyses were performed by using SPSS for Windows 13.0 (SPSS Inc, Chicago, IL, USA). Continuous variables were presented as mean ± SD and categorical variables were shown in absolute numbers or percentages. Differences between NGT, IGR, and diabetes groups were assessed by Chi-square test for categorical and ANOVA for continuous variables. Correlation between Gensini score and continuous variables was determined by Pearson correlation coefficients. Stepwise adjustments included: 1) age and gender, 2) smoking status, family history of CHD, history of atrial fibrillation, history of hypertension, BMI, WHR, SBP, and DBP, 3) lipid profile and creatinine. Multiple linear regressions were performed to evaluate the associations between Gensini score and glycemic variables. Confounders adjusted in linear regressions included age, gender, smoking status, family history of CHD, history of atrial fibrillation, history of hypertension, BMI, WHR, SBP, DBP, lipid profile, creatinine, and duration of diabetes. Logistic regressions were also performed to evaluate the associations between the presence of coronary heart disease and glycemic variables. In all analysis, P < 0.05 was considered statistically significant.
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3

Fingerprint-Activity Relationship in Salvia miltiorrhizae

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Multiple linear regression analysis (MLRA) is usually used to model the best combination of two or more independent variables (xi) to predict or estimate the dependent variable (Y) by fitting a linear equation. It shows the contribution of each independent variable to the dependent variable in the following form: Y=b0+i=1nbixi(n=1,2,3,4) where Y is the estimated value and represents the dependent variable and xi are the uncorrelated variables; b0 represents the estimated constant, and bi is called the regression coefficients. In this study, MLRA was introduced to combine data from the chemical fingerprints (peak area of each component) and biothermal activity (main quantitative thermo-kinetic parameters) of S. miltiorrhizae samples on P. aeruginosa. This allowed us to establish the fingerprint-activity relationships using SPSS statistical software (SPSS for Windows 13.0, SPSS Inc., USA), to further explore the active components of S. miltiorrhizae that primarily contributed largely to the anti-P. aeruginosa activity.
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4

Statistical Analysis of Experimental Replicates

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All data acquired in this study were generated from at least three replicates of independent experiments using identical protocols. One-way analysis of variance (ANOVA) or T-tests were performed using SPSS for Windows 13.0. The data were expressed as means ± SEM; P values < 0.05 and P values < 0.001 were considered significant and highly significant, respectively.
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5

Genetic Associations in Disease Risk

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The age of cases and controls was compared using the student's t-test. Hardy–Weinberg equilibrium was tested using Chi-square test. The χ2 test, with odds ratio (OR) and respective 95% confidence intervals (CIs), were used to estimate the differences of genotype and allele distribution. MiR-34b/c and TP-53 mRNA expression levels were evaluated using Wilcoxon rank sum test. The statistical analyses were performed using the SPSS for windows 13.0 (SPSS Inc, Chicago, IL). Moreover, genotypic association tests in a case–control pattern, assuming codominant, dominant, recessive, and overdominant genetic models were calculated using SNPstats.32 A P level of <0.05 was regarded as statistically significant.
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6

Statistical Analysis of Delay Factors

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Statistical analysis of the data was carried out by the SPSS for Windows 13.0 (SPSS, Inc., Chicago, IL, USA). Qualitative variables were presented as number and percentages. Quantitative variables were presented as mean ± standard deviation for variables with normal distribution, and as median and interquartile range (IQR) for variables with skewed distributions. Chi2 tests and Fisher test were used to identify factors associated with different delays. A multivariate logistic regression was used to determine factors associate with longer delay. In all tests, the values p < 0.05 were regarded statistically significant.
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7

Statistical Analysis of Survey Data

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For a statistical analysis of data obtained during the survey a base in the statistical program SPSS for Windows 13.0 was created. During the computer analysis, statistical methodologies were used as follows:

- Distribution of frequencies (absolute and relative representation) to present the categorical variables;

- Descriptive methods (measures of central tendency - average, median, minimum, maximum values to present the quantitative variables;

- To test the significance of differences between the analysed groups non-parametric (Chi-square test, Fisher exact test, Mann-Whitney U test), and parametric tests (t-test for independent samples, Analysis of Variance) were used depending on the nature of the data i.e. their distribution;

- As a level of significance or importance was taken a value of p <0.05, and as a highly significant value of p <0.01.

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8

Cardiac Pathologies and Arrhythmia Analysis

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Frequency outcomes including the incidence of cardiac pathologies and arrhythmia were analyzed by Chi square test and values presented both as counts and percentage. Quantitative data were analyzed by two-way ANOVA, in which feed intake manipulation (Ad or R) and 25-OH-D3 treatment were the classifying variables. Differences between group means were tested using Bonferroni t test when the main effect was significant. In cases where a significant interaction between feed intake and 25-OH-D3 treatment was found, a mean comparison was performed. Quantitative values were expressed as means ± SEM. Organ weights were reported as absolute weights (grams) and as a fraction of BW (g/100 g BW). The presence of possible correlation between actual and fractional heart and liver weights in hens experiencing SD were calculated using Pearson’s correlation method. Mean differences were considered significant at p < 0.05. All statistical procedures were carried out using SPSS for Windows 13.0.
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9

Statistical Analysis of Experimental Data

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Statistical analysis was performed with SPSS for Windows 13.0 (SPSS Inc., Chicago, IL, USA). Data were described with mean ± standard deviation (range) or number (percentage) unless stated otherwise. Mann-Whitney rank-sum test was used for comparison between two groups and Kruskal-Wallis one-way analysis of variance on ranks among three or more groups. Spearman's rank order correlation test was used to assess the correlation between two variables. P < 0.05 was considered statistically significant unless stated otherwise.
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10

Statistical Analysis of Experimental Data

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All statistical analyses were performed using SPSS for Windows 13.0 (SPSS Inc., Chicago, IL, USA). Data represented results from 3 or more experiments. Statistical significance was determined by Student’s t-test, and a p value of <0.05 was considered significant.
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