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Spss 16.0 for window

Manufactured by IBM
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SPSS 16.0 for Windows is a statistical software package that provides data management, analysis, and reporting capabilities. It is designed to help users explore data, model relationships, and generate reports. The software supports a wide range of data types and offers a variety of statistical techniques, including descriptive statistics, regression analysis, and multivariate analysis. SPSS 16.0 for Windows is a powerful tool for researchers, analysts, and decision-makers who need to gain insights from their data.

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634 protocols using spss 16.0 for window

1

Dietary Manganese Supplementation in Ducks

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Replicate (each replicate containing 14 cages, one duck in each cage) served as the experimental unit for analysis of performance and egg quality data; the average of 2 ducks in each replicate was the experimental unit for other assessment. The normality of the data and homogeneity of variances were first verified by Explore procedure using SPSS 16.0 for Windows (version 16.0; SPSS Inc., Chicago, IL). The effects of dietary Mn supplementation were analyzed using the one-way ANOVA procedure, and then, regression analysis was used to test the linear and quadratic effects using SPSS 16.0 for Windows. Quadratic regressions (Y = aX2 + bX + c) were fitted to the responses of the dependent variables to Mn supplementation. The dietary concentration of Mn at which the response first reached 95% of the maximum was used to estimate the requirement (Zhang et al., 2020b (link)). Data are expressed as means and pooled SEM.
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2

Comparing Bone Debris in Surgical Outcomes

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The initial set of analyses compared demographics, age and body mass index (BMI), of the two groups. These comparisons were performed using the unpaired t-test (SPSS 16.0 for Windows). The outcome of interest was the presence, or not, of bone debris on the post-operative radiographs. Due to the categorical nature of this outcome, the analysis was performed using the Chi-squared test (SPSS 16.0 for Windows).
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3

Duck Performance and Egg Quality Study

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Replicate (each replicate containing 12 cages, 2 ducks in each cage) served as the experimental unit for analysis of performance and egg quality data; the average of 2 ducks in each replicate was the experimental unit for other assessments. The normality of the data and homogeneity of variances were first verified by the Explore procedure using SPSS 16.0 for Windows (SPSS Inc., Chicago, IL ). The effects of dietary CP levels were analyzed by one-way ANOVA procedure, and then means were compared using Tukey's multiple range tests. Regression analysis was employed to test the linear (L) and quadratic (Q) effects using SPSS 16.0 for Windows (SPSS Inc.). Data are expressed as means and pooled SEM.
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4

Comparative Analysis of Secologanic Acid

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In order to observe the classification and assess the variation of LJF and LF, the scatter plot of all the samples including LJF and LF was made according to the amount of secologanic acid using GraphPad Prism 5 software. The rank sum test was utilized to confirm that there were differences in the amount of secologanic acid between LJF and LF (SPSS 16.0 for Windows, IBM, Armonk, NY, USA).
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5

Statistical Analysis of Oncological Outcomes

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Statistical analyses were performed using SPSS 16.0 for Windows (IBM, Armonk, NY, USA). Quantitative data were compared between groups using Student’s t-test. Categorical data were analyzed by the χ2 test or Fisher’s exact test. OS and RFS rates were calculated according to the Kaplan–Meier method, and differences were analyzed using the log-rank test. Univariate and multivariate analyses were performed using the Cox proportional hazards regression model. P<0.05 was considered statistically significant.
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6

Diagnostic Accuracy of CRSwNP

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Differences between groups were assessed by ANOVA. In all cases, P < 0.05 was considered statistically significant. We drew a receiver operator characteristic (ROC) curve to calculate the area under curve (AUC) to discriminate CRSwNP patients from normal subjects. SPSS 16.0 for Windows (IBM, Chicago, USA) was used for ROC analyses and other statistical analyses were performed using GraphPad Prism 7.0 software (GraphPad Software, La Jolla, CA).
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7

Statistical Analysis of Genetic Variants

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Statistical analyses were performed using SPSS 16.0 for Windows (IBM, Chicago, IL). After assessing the normality of the distribution of the continuous variables, they were compared either by a Student’s t-test or one-way ANOVA with LSD post hoc analysis, or using a Mann–Whitney U test or Kruskal–Wallis H test, for those with normal and non-normal distributions, respectively. The correlations between the continuous variables were assessed using a Pearson’s correlation test.
The differences in genotype distribution between the patient and control groups were assessed with χ2 tests in 2 × 2 contingency tables. The odds ratios (OR) and 95% confidence intervals (CI) were obtained by applying the binary logistic regression. Outputs with p < 0.05 were considered statistically significant.
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8

Classifying and Differentiating Ophiopogonis Radix via PCA and PLS-DA

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PCA, an unsupervised pattern recognition method, has been used for quality control of traditional Chinese medicine. According to the contents of 32 components, PCA was applied to classify and distinguish Ophiopogonis Radix from different habitats by Simca-P 13.0 software (Umetrics AB, Umea, Sweden). In addition, PLS-DA was performed to differentiate CMD and ZMD and find the differential constituents with variable importance in the projection (VIP) values. Besides, all detected components data were statistically analyzed by t-test (SPSS 16.0 for Windows, IBM, Armonk, NY, USA), which was used to find the differential constituents for the classification between CMD and ZMD. According to the results of quantitative determination and t-test, the boxplots were charted by Origin pro 8 (Origin Lab, Northampton, MA, USA) to obtain an overview of the metabolite distribution and analyze the discrimination of CMD and ZMD. GRA can compensate for the shortcomings in statistical regression by Grey analysis, and be applied to evaluate the samples quality by measuring the approximate correlation between sequences. GRA was carried out to evaluate the quality of CMD and ZMD based on the contents of 32 constituents.
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9

Propensity Score Matching for Bias Reduction

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SPSS 16.0 for Windows (IBM, Armonk, NY) was used for analysis. To minimize the impact of potential confounders and selection bias, propensity score analysis was used to compensate for the differences in baseline patient characteristics between the two groups of patients. Patients in the two groups were 1:1 matched using the nearest propensity score on the logit scale. Variables that could influence the outcomes of treatment were matched, including age, gender, body mass index (BMI), ASA status class, and maximal lesion size. After PSM, differences in continuous and categoric clinical characteristics were compared.
Continuous data are presented as mean and SD and were analyzed with two-sample Student’s t tests for independent data. Categorical variables are given as a count and percentage of patients and analyzed with the χ2 or Fisher’s exact test. All tests were two-sided, P-values < 0.05 were considered statistically significant. SPSS Statistics 16.0 (IBM Corp, Armonk, NY) was used for statistical evaluations.
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10

Complement C1q Levels in Major Depressive Disorder

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The baseline demographic characteristics between MDD group and healthy controls were compared by applying the Chi-square test for gender and Mann–Whitney U-test for age. As data of C1q levels were not normally distributed, nonparametric tests were used in this study. Differences in the complement C1q levels between patients with MDD and the controls, as well as between sexes among patients with MDD and the controls, were assessed using Mann–Whitney U-test. Spearman nonparametric correlations were obtained between complement C1q levels and age. All tests were two-tailed, with statistical significance defined as P < 0.05. Statistical analyses were performed using SPSS 16.0 for Windows (IBM Corp, Chicago, America).
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