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Spss version 19.0 statistical

Manufactured by IBM
Sourced in United States

SPSS version 19.0 is a statistical software package that provides advanced analytical capabilities. It is designed to help users analyze and interpret data, enabling them to make informed decisions. The software offers a wide range of statistical techniques, including regression analysis, factor analysis, and time series analysis, among others. SPSS version 19.0 is widely used in various industries and research fields to gain insights from data.

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11 protocols using spss version 19.0 statistical

1

Evaluating Surgical Outcomes using SPSS

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The SPSS version 19.0 statistical software package was used for data analysis. Measurement data, including the VAS and QuickDASH scores, grip strength, and wrist mobility, were evaluated based on the ROM. Preoperative and postoperative data were compared using the paired t-test; p < .05 was considered statistically significant. All data have been presented as means with standard deviation.
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2

Genomic Biomarkers for Survival Outcomes

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Hardy-Weinberg equilibrium (HWE) assumption was calculated by Chi-squared test for each SNP. The association between clinical and molecular variables was analyzed by crosstabs and Pearson’s chi-squared tests (χ2), while odds ratio (OR) and 95% confident intervals were calculated by logistic regression analyses. OS and PFS-related endpoints were estimated using the Kaplan-Meier method. To evaluate the effect of each SNP for each OS endpoint, Cox’s proportional hazards (PH) regression was used, adjusted by Ki67 index. Cytokines and serum biomarkers were treated as time-dependent variables [36 (link)]. Fisher’s exact test was applied to compare categorical variables. Statistical hypothesis testing for continuous variables was performed using the Mann-Whitney U test (due to the non-normality of these variables). Paired data were compared with the Wilcoxon Signed-Rank Test. All statistical assessments were two-sided and p-values<0.05 were deemed significant. Given the exploratory nature of the study in a field for which no published data were available during the design phase, no statistical tool was applied to calculate sample size. Furthermore, for the same reason, corrections for multiple comparison were performed only for the effect of circulating biomarkers on response. The SPSS version 19.0 statistical software package was used.
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3

Cell Culture Data Analysis

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Data were expressed as mean ±SEM from two independent experiments using different cultures. Each experiment was performed at least in triplicate with different cell batches (total 6–12 measurement/condition). Statistical analyses were performed using SigmaPlot 11.0 software. Data were tested by One Way ANOVA followed by the Bonferroni test. Differences were considered significant at P<0.05. SPSS version 19.0 statistical analysis package (SPSS, Inc., Chicago, IL, USA) was used for the PCA test and linear correlations.
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4

Survival and Recurrence Analysis Protocol

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Statistical analyses were performed using SPSS version 19.0 statistical software. Normally distributed continuous data are presented as mean and standard deviation, while abnormally distributed data are presented as median and interquartile range. Categorical data are presented as frequencies and percentages. Survival curve and recurrence‐free curve were calculated using the Kaplan‐Meier method. A multivariate Cox regression analysis was performed to analyze prognostic factors of survival and recurrence‐free status. Uni‐ and multivariate logistic regression analyses were performed to analyze the predictive factors of postoperative myasthenic crisis (POMC). P‐values <0.05 were considered statistically significant.
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5

Comparative Statistical Analysis Workflow

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All statistical analyses were performed using SPSS version 19.0 statistical software (SPSS, Inc., Chicago, IL). Quantitative data are expressed as ( ±s). A t test was used to compare differences between 2 groups. P < 0.05 was considered statistically significant.
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6

Prognostic Value of D-dimer Levels

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Statistical analysis used the SPSS version 19.0 statistical software. Survival analysis was performed using the Kaplan–Meier method, and the log-rank test was used for analysis. Univariate and multivariate analyses were performed using Cox's proportional hazards model. The relationship between D-dimer levels and clinicopathological features were analyzed using χ2 test. The data are expressed as the mean±SEM, and P value < 0.05 was considered statistically.
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7

IC50 Calculation and Statistical Analysis

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The half maximal inhibitory concentrations (IC50) for AG and 2-BEA were calculated using GraphPad Prism 6.0 software (GraphPad, San Diego, CA, USA), and statistical analyses were performed using SPSS version 19.0 statistical software (SPSS Inc., Chicago, IL, USA). Data were expressed as mean ± standard deviations (SD). One-way analysis of variance was used to compare the differences among groups. Values of P < 0.05 were considered statistically significant.
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8

Stent Patency and Survival Analysis

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Statistical analyses were performed using SPSS version 19.0 statistical software. Data that were normally distributed are expressed as the mean ± SD, while those with a non-normal distribution are expressed as the median, and independent sample t-test was performed. The Kaplan-Meier method was used to compare the stent patency time and survival time. Cox proportional hazard regression analysis was used to analyze the risk factors affecting the prognosis of patients. P < 0.05 was considered statistically significant.
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9

Statistical Analysis of Experimental Data

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All statistical data were analyzed using SPSS version 19.0 statistical software (SPSS, Chicago, IL USA), and the values are expressed as the mean ± standard deviation. Multiple comparisons between groups were performed by one-way ANOVA, and post hoc analyses were conducted using the least significant difference test. The differences between groups were considered significant at a p < 0.05.
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10

Amyloid vs. Non-Amyloid Kidney Pathology

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Analysis was performed with the SPSS version 19.0 statistical software package (SPSS, Chicago, IL). Continuous data were expressed as means with standard deviations (SDs) or as medians with interquartile ranges (IQRs). Categorical data were presented as proportions. Patients were divided into two groups on the basis of their kidney pathology: amyloid and non-amyloid. Differences between groups were compared using t-test for normally distributed and homogeneous quantitative data, Mann–Whitney U test for non-normally distributed, heterogeneous quantitative and semiquantitative data, and Fisher’s exact test for polychotomous data. Patient survival and renal survival were estimated by the Kaplan–Meier method. Kaplan–Meier analysis was used to compare survival between amyloid and non-amyloid patients. Possible indicators for death and renal endpoint were examined by univariate analysis (log-rank test and Cox post hoc for calculation of hazard ratio, HR). The small number of patients/events did not permit multivariate analysis of overall survival or renal survival. All tests were two-sided, and P < 0.05 indicated statistical significance.
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