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Spss statistics 22.0 for windows

Manufactured by IBM
Sourced in United States

SPSS Statistics 22.0 for Windows is a comprehensive software package designed for statistical analysis. It provides a wide range of statistical techniques and tools for data management, analysis, and presentation. The software supports a variety of data formats and offers features for data exploration, modeling, and reporting.

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86 protocols using spss statistics 22.0 for windows

1

Somatic MCPH1 Depletion Analysis

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χ2‐test was used to compare PCC phenotype frequency between mutant and control cells and to compare the frequency of somatic TP53 and PIK3CA mutations in somatically MCPH1‐depleted and wild type breast tumors. Independent samples two‐tailed t‐test was used for comparison of means of 3D spheroid sizes, number of G1 phase cells in flow cytometry, number of migrated and invaded cells in transwell assays and chromosome condensation times in live‐cell imaging. Statistical analyses were performed using IBM SPSS Statistics 22.0 for Windows (IBM Corp.) and p‐values <0.05 were considered significant.
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2

Pressure Pain Threshold Evaluation

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For the study design, a sample size calculation was carried out using the program nQuery. The data obtained were transferred to Excel (Microsoft) and collected. IBM SPSS Statistics 22.0 for Windows was then used for the statistical evaluation and the creation of tables and graphics. The statistical processing of the metric variables was initially carried out using descriptive statistics. Means, standard deviations and 95% confidence intervals were calculated and presented. The groups were tested for homogeneity with regard to gender, age and BMI using the Chi² test and the t-test. Furthermore, mean differences of the pressure pain thresholds were analyzed with the help of two-sided t-tests for paired and unpaired samples. Missing values were excluded list by list. The test for equality of variance of the groups presented was carried out in each case using Levene’s test. In order to determine the pairwise correlation of the individual test characteristics with each other, bivariate correlations were carried out using Pearson’s correlation coefficient. The significance level was set at p < 0.05 in the study design.
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3

Abnormal Data Statistical Analysis

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Shapiro–Wilk test was used to find out whether the data were normally distributed. They were found to be abnormally distributed. Wilcoxon paired 2 sample test was used for the analyzes of data. Correlations were calculated with Spearmen Rho coefficient. A level of p<0.05 was considered as statistically significant. IBM SPSS Statistics 22.0 for Windows package program was used for statistical analysis.
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4

Statistical Methods for Bioinformatics Analysis

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All variables were analyzed using IBM SPSS Statistics 22.0 for Windows. The Independent-samples T test was used to analyze the measurement data and X2 test count data. Fisher’s exact test was used under conditions of n < 40 or any T < 1, and Yates’ correction for continuity was used under conditions of n ≥ 40, 1 ≤ any T ≤ 5 for the 2*2 table X2 test. Survival analyses were performed using the Kaplan-Meier method with the log-rank test. P < 0.05 was set as a statistically significant difference.
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5

Statistical Analysis of Cost Data

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The cost data had a non-normal and skewed distribution. Accordingly, regression analysis of costs was performed by using a generalized linear model (GLM) with the assumption of a gamma shaped distribution of the dependent variable [23 (link)]. GLMs are generally well suited for statistical analysis of cost data, which often show a high degree of non-normality.
We used a two-step procedure. First, logistic regression with costs as binary outcome was performed in order to understand which of the factors that was associated with the highest costs. Second, a GLM model was run to explore the magnitude of the cost-driving factors. In the GLM, the cost driving factors were dichotomized and first entered separately. All models were adjusted for age, gender and education. In the joint analysis, all factors were entered simultaneously. Dementia diagnosis is included in the Charlson Comorbidity Index, but in the joint analysis, dementia was analyzed as a separate variable and, thus, was removed from the index. Results of the GLM are expressed as relative change in cost due to increase in the explanatory variable (e.g. dementia). Inclusion of site (i.e. Kungsholmen and Nordanstig) did not affect the results; therefore, this variable was not included in the analyses. IBM SPSS Statistics 22.0 for Windows (IBM corp., New York, NY, USA) was used for the analyses.
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6

Statistical Analysis of Biomedical Data

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For descriptive statistics, continuous and non-normal variables were summarized as average, standard deviation (SD), median and interquartile range (IQR); 25th to 75th percentiles were calculated to measure the statistical dispersion of the data; categorical variables were summarized as frequency and percentage. The Shapiro-Wilk test was used to evaluate normality for all variables. The Kolmogorov-Smirnov test was performed to define the correspondence of each parameter with a normal or non-normal distribution. The Independent Samples t Test was used to compare the means of two independent groups, considering the level of statistical significance (p value < 0.05). The Pearson linear correlation coefficient (r) was used to investigate the strength of the association between two quantitative variables considering the level of statistical significance (p value < 0.05). The Mann-Whitney U test was used to probe the influence of categorical variables on continuous ones, considering the level of statistical significance (p value < 0.05). All tests were performed with IBM SPSS Statistics 22.0 for Windows (Chicago, IL, USA).
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7

Statistical Analysis of Experimental Data

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Statistical analysis was performed using IBM SPSS Statistics 22.0 for Windows (IBM Corp., Armonk, NY, USA). Measurement data are represented as mean ± standard deviation. The mean differences among the groups were analyzed using a one-way analysis of variance, and the comparisons of count data between the groups were tested using a chi-square test. P < 0.05 was considered statistically significant.
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8

Statistical Analyses of Experimental Data

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Statistical analyses were carried out with IBM SPSS Statistics 22.0 for Windows. The results are expressed as means ± standard deviations. Normality was tested with the Shapiro-Wilk test. A two-way ANOVA was used to show differences between study variables. The level of significance was set at p < 0.05.
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9

Biostatistical Analysis of Experimental Data

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All continuous variables were expressed as mean ± standard deviation, categorical variables were expressed as number (percentage). The normality of variables was tested using the Shapiro–Wilk method. Group comparisons were performed by Student’s unpaired 2-tailed t-test or by Mann–Whitney U test, as appropriate. A p value < 0.05 was considered statistically significant.
Data management and analysis were performed using IBM® SPSS® Statistics 22.0 for Windows® software (IBM Corporation, New Orchard Road Armonk, New York, NY, United States).
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10

Statistical Analysis of Experimental Data

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Statistical analysis was performed with SPSS Statistics 22.0 for Windows (IBM, Armonk, NY, USA). All values were expressed as means ± standard deviations. Differences between the groups were assessed using one-way analysis of variance (ANOVA). Tukey’s honestly significant difference (HSD) test was used to determine the group that caused these differences. Additionally Student’s t test was performed to analysis of the datas between controls and test animals. A value of P < 0.05 was considered statistically significant.
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