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Spss statistics software version 20

Manufactured by IBM
Sourced in United States

SPSS Statistics software version 20 is a data analysis tool used for statistical analysis. It provides a comprehensive set of features for data management, analysis, and reporting. The software is designed to help users analyze and interpret data from a variety of sources, including surveys, experiments, and observational studies.

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287 protocols using spss statistics software version 20

1

Comparative Analysis of Cow Data

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The data of the four groups of cows were collected and analyzed. Data are presented as the means and the standard error of the mean (SEM). Significant differences were determined through one-way analysis of variance and Tukey’s multiple comparison tests. Data were statistically analyzed using SPSS Statistics software, version 20.0 (IBM Corp., Armonk, NY, USA). Statistical significance was defined at p < 0.05, with highly significant values at p < 0.01.
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2

Differential Expression of Luminal and Basal Markers in Papillary Bladder Cancer

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Differential expression of luminal and basal protein markers in matched pairs of exophytic and stroma-invasive tumor areas of pure papillary pT1(a) HG carcinomas was assessed using the Wilcoxon matched-pairs signed rank test in GraphPad Prism 7.0 (GraphPad Software, San Diego, California). In order to correlate ERBB2 genomic FISH and ERBB2 protein expression data, as well as cytokeratin expression, a two-tailed Fisher’s exact test was conducted applying SPSS Statistics software version 20.0 (IBM, Armonk, New York). For all analyses the level of significance was set to p < 0.05.
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3

Neuromuscular Assessment in Animal Model

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Data were expressed as mean ± SD values in each group. The Kolmogorov-Smirnov test was used to check for normal distribution of the data, and the Kruskal-Wallis test was performed to compare performances of each group in grooming test, muscle force and weight, and electromyography. Dunn’s test was used as a post hoc test when groups were significantly different (P < 0.05). A Mann-Whitney test was used to compare the axon counts between groups. A P value < 0.05 was considered statistically significant. Statistical analysis was performed with IBM SPSS Statistics software, version 20.0 (IBM, released 2011, Armonk, N.Y.) by the Biostatistical Center for Clinical Research, Chang Gung Memorial Hospital, Linkou, Taiwan.
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4

Predicting Neurological Outcomes from EEG

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Statistical analyses were based on the IBM SPSS statistics software version 20.0 (Inc.; IL; USA). A descriptive analysis for each variable was first performed. Comparison between groups with good (CPC1-2) and bad (CPC 3-4-5) outcomes was carried out using the Pearson Chi2 test for qualitative variables and the Mann Whitney test for quantitative variables. For each variable and EEG feature, sensitivity (Se), specificity (Sp), positive predictive value (PPV), and negative predictive value (NPV) for predicting an unfavorable outcome were calculated. We also performed a multivariate analysis by logistic regression to determine which EEG patterns could predict neurological outcome. A maximum of five EEG patterns were included in each model tested.
The concordance strength between EEG readers was based on the kappa score nomenclature of Landis and Koch (Landis and Koch, 1977 (link)) which defines the agreement according to the kappa value (<0: Poor; 0–0.2: Slight; 0.21–0.40: Fair; 0.41–0.60: Moderate; 0.61–0.80: Substantial; 0.81–1: Almost perfect) (ref).
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5

Cardiovascular Risk in Rheumatoid Arthritis

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Baseline characteristics of the RA cohort and incidence of CV events were presented by appropriate descriptive statistics. COX regression analysis was performed to determine CV event risk and contributing risk factors over time. Statistical analyses were performed using IBM-SPSS statistics software version 20.0.
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6

Statistical Analysis of Research Data

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The mean values and standard error of the mean were evaluated using IBM SPSS Statistics software, version 20.0 (IBM Co., Armonk, NY, USA).
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7

Gut Microbiome and Metabolite Analysis

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Statistical analyses were done with SPSS Statistics software version 20.0 (IBM Corp., Armonk, NY, USA). The Kruskal–Wallis test was used to assess the significant differences in the microbial phyla and genera between the two groups. A t-test was performed to assess the differences in pH, VFA, lactate, and metabolite levels. Statistical significance was declared at P < 0.05. The P values of the metabolomics and microbial data were corrected using a false discovery rate (FDR). The FDR-corrected P -values below 0.05 were considered statistically significant.
A partial least squares discriminant analysis (PLS-DA) was accomplished with SIMCA-P software. The PLS-DA was determined by the goodness-of-fit parameter (R2X) and the predictive ability parameter (Q2). Based on the PLS-DA results, the metabolites were plotted in accordance with their importance in the separation. Every compound had a value—the variable importance in the projection (VIP)—where VIP > 1.0 indicated that a metabolite was significantly different. The Spearman’s rank correlation coefficient was calculated with GraphPad Prism software version 6.00 (GraphPad Software, San Diego, CA, USA) to evaluate the metabolites and microbiota.
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8

Comparative Analysis of SF36 and IPAQ

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The statistical analysis of this work was performed using IBM® SPSS Statistics software version 20.0. Fisher’s exact test was used to compare categorical variables. For normally distributed variables, we used Student’s t-test. For non-parametric variables, we used the Mann–Whitney U-test. SF36 variables and IPAQ scores were compared with Pearson’s correlation. The level of significance adopted for this research was p < 0.05. Post hoc power analysis was performed using the G*power program [36 (link)]. When analyzing the physical and mental components of the SF36 summary scores, we obtained effect sizes (d) of 1.75 and 1.37, respectively.
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9

Reliability Assessment of Stroke Imaging

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All reliability analyses were performed using Krippendorff’s alpha (K-alpha) with 1000 bootstrap samples for each. K-alpha results range from −1.0 to +1.0 where +1.0 equates to perfect agreement, 0.0 means no agreement and −1.0 implies perfect disagreement [20 (link)]. We have adopted the Landis and Koch approach for interpreting these results such as K-alpha 0.00–0.20 = slight agreement, 0.21–0.40 = fair agreement, 0.41–0.60 = moderate agreement, 0.61–0.80 = substantial agreement and 0.81–1.00 = almost perfect agreement [21 (link)]. Differences in K-alpha between expert and non-expert groups (including between neuroradiology specialist trainees and others) and between imaging characteristics assessed on NCCT and CTA were not tested for significance.
All analyses were performed using IBM SPSS Statistics software, version 20.0 (IBM Corporation, Armonk, NY, USA). SPSS does not provide native support for K-alpha; an appropriate macro was applied [22 ].
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10

Genetic Associations with IL-35 Analysis

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Pearson’s chi-square test was used to analyze deviation from Hardy-Weinberg equilibrium (HWE). We used the Open Source Epidemiologic Statistics for Public Health software, version 3.01, for the estimation of sample size and power of study. Chi-square test was used for comparing categorical variables. The association between IL-35 and demographic data was analyzed using multivariable logistic regression and adjusted for other covariates. P<0.05 was considered statistically significant. Statistical analysis was performed using the IBM SPSS Statistics software, version 20.0 (SPSS Inc., Chicago, Illinois, United States of America).
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