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Spss 16.0 version software

Manufactured by IBM
Sourced in United States

SPSS 16.0 is a software application for statistical analysis. It provides a range of statistical procedures for data manipulation, analysis, and presentation. The software is designed to handle a variety of data types and offers a user-friendly interface for conducting analyses.

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6 protocols using spss 16.0 version software

1

Comparing 2D and 3D Brachytherapy Planning

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All tumor and OAR DVH parameters were examined to ensure approximately normal distributions. The results were calculated as mean± standard deviation. The DVHs for the tumors and OARs were compared between 3D and 2D BT planning using the pair t-test; and for the comparison between the small and big tumors in 2D and 3D BT planning, respectively, unpaired t-test was used. SPSS 16.0 version software (SPSS Inc., Chicago, IL, USA) was used for statistical analysis, and a p-value of <0.05 was considered statistical significant.
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2

Urinary Liver-Type Fatty Acid-Binding Protein Analysis

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All statistical analyses were performed using Statistical Package for the Social Sciences (SPSS) 16.0 Version software (SPSS Inc., IL, USA). Mean and standard deviation for continuous variables and percentages for categorical variables are reported as relevant. u-LFABP showed a skewed distribution and are reported as a geometric mean (95% confidence interval) Significant differences between groups were tested using the χ2-test and Analysis of variance where ever appropriate. The relationship between u-LFABP and the other variables of study subjects was tested by Pearson correlation test. A P<0.05 was considered as statistically significant.
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3

Statistical Analysis of Experimental Data

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Data were statistically analyzed by SPSS 16.0 version software (SPSS Inc., United States), expressed as mean ± standard deviation (SD). Graphs were created using GraphPad Prism 8.
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4

Statistical Analysis of Viral Infection

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SPSS 16.0 version software was used to perform statistical analyses. The Mann–Whitney test was used to statistically compare the E38-ORF7 CPD and E38 original virus groups. Prior to analysis, the values were log transformed for viremia. The normality of the distribution of the examined variables was evaluated by the Shapiro–Wilk test. Continuous data were compared between groups using the Student’s t test followed by a one-way analysis of variance. Lung microscopic and respiratory scores were compared by the non-parametric Mann–Whitney test. All data are expressed as the mean ± standard deviation. For all statistical analyses, p < 0.05 was considered significant.
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5

Statistical Analysis of Experimental Data

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Statistical analysis was by Student’s t-test, ANOVA or Mann–Whitney U-test according to data distribution using version 16.0 SPSS software (SPSS Inc. Chicago, IL, USA). The data are presented as the mean ± standard deviation (SD). Analysis of correlation between variables was performed by linear regression analysis with Prism Version 5 software (GraphPad). A p value <0.05 was considered statistically significant.
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6

Comprehensive Statistical Analysis of Biological Experiments

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All values have been evaluated with version 16.0 SPSS software (SPSS Inc., Chicago, IL, USA). The reports were provided as the mean ± S.D. for each condition of at least three independent experiments and checked for using the parametric or nonparametric post hoc analysis. In addition, the raw data of flow cytometry and real-time PCR were analyzed with the FSC Express 5 and Rest 2009 software, respectively. Thus, one-way variance analysis (ANOVA) and the Tukey test were carried out to investigate group variations. Statistically, significant differences have been taken into account at p < 0.05, 0.01, and 0.001.
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