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Spss statistics for mac version

Manufactured by IBM
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SPSS Statistics for Mac, Version is a statistical software package developed by IBM for data analysis. It provides a range of statistical and analytical tools to help users explore, analyze, and visualize data. The software is designed to run on macOS systems and offers a user-friendly interface for conducting statistical analyses.

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10 protocols using spss statistics for mac version

1

Comparative Analysis of Novel Therapeutics

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Statistical analysis was carried out using SPSS 28.0 (IBM Corp., Armonk, NY, USA. Released 2021. IBM SPSS Statistics for Mac, Version 28.0). The multiple comparison of means was performed by ANOVA followed by Tukey’s post hoc test at a confidence level of 0.95. Graphics were made using GraphPad 10.0 (GraphPad Prism Software for Mac, Version 10.0, San Diego, CA, USA). Schemes were created with Biorender.com (accessed on 10 January 2024).
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2

Neurochemistry of Parkinson's Dyskinesia

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We used IBM® SPSS® Statistics for Mac (Version 25.0) for the statistical analyses. Partial correlations between extracted grey matter volumes in the motor ROI and severity of dyskinesia (AIMS sum score of 10 items) and parkinsonism (mean of SAS single scores) were calculated and deemed significant at P < 0.05, corrected for 26 (multiple) comparisons using the false discovery rate (FDR).17 A Spearman correlation analysis was performed for each of the 11 receptors/transporters provided by the JuSpace toolbox correlating its spatial distribution with local grey matter volumes on the group level using the Neuromorphometrics atlas. We used the default option accounting for spatial autocorrelation. Spearman ϱ correlation coefficients were Fisher’s z-transformed. Receptors showing a significant [P < 0.01, FDR corrected for 11 (multiple) comparisons] association with grey matter volumes were entered into a multiple linear regression analysis to disentangle their specific associations.
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3

Profiling miRNA and mRNA in Cancer Therapy

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Sociodemographic and clinical characteristics are presented using means and SDs for continuous variables and frequency distributions for categorical variables. We used log 2-transformed data for all miRNA and mRNA expression values. For each miRNA, we compared expression at each timepoint (week 0 and 2) with a repeated-measure ANOVA to identify those that changed significantly over time. For these miRNAs, we assessed the association between the change of expression of each miRNA (between week 0 and week 2) and course of intensity of each side effect between week 0 and week 2 (dependent variable) using linear regressions. To assess the role of miRNAs on predicted mRNA targets, we identified negative associations between week 0 and week 2 using linear regressions. For mRNA, we assessed the change of expression between week 0 and week 2 using a repeated-measure ANOVA. We used a false discovery rate threshold of 5% for each multiple comparison. Statistical analyses were performed with SPSS 25.0 (IBM Corp., released 2017. IBM SPSS Statistics for Mac, Version 25.0. Armonk, NY).
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4

ABCA7 Genotype, Cognition, and Sleep Quality

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To examine the main effects of ABCA7 genotype (risk versus non-risk) on cognition and the moderating role of sleep quality (poor, average, good), a univariate analysis of covariance (ANCOVA) was conducted, with ABCA7 genotype and sleep quality as fixed factors and age and years of education as covariates. Any significant interactions were explored further with simple main effects analysis (with Bonferroni correction for multiple comparisons) as described in the Results section below. All assumptions for ANCOVA were checked and met prior to analyses. All statistical analyses were performed using IBM SPSS® Statistics for Mac, version 28.0.1.1 (IBM Corp., Armonk, NY, USA).
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5

Exam Performance Analysis: Randomized Study

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Data were analysed with descriptive statistics and presented as means with corresponding standard deviations (s.d.) as well as by medians with interquartile ranges (IQR).
An intention-to-treat (ITT) analysis was performed, to guarantee that the randomisation remains unbroken. Missing data were replaced by the median values of the group to which participants were originally allocated (Hollis & Campbell 1999 (link)). To determine differences in the exam results between the G-SS-G and CG after the first semester, the Mann-Whitney U test was used using the exact sampling distribution of U (Dinneen & Blakesley 1973 (link)). All calculations were performed using the Statistical Package for Social Sciences (SPSS) version 27.0 (IBM Corp. Released 2020. IBM SPSS Statistics for Mac, Version 27.0. Armonk, New York, United States: IBM Corp.)
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6

RLS Severity: Multimodal Treatment Assessment

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The analysis was done using Statistical Package for Social Sciences (SPSS) v 28.0 (IBM Corp. Released 2021. IBM SPSS Statistics for Mac, Version 28.0.1.0 (142) Armonk, NY: IBM Corp.) Analysis was done using two methods - per protocol and intention to treat (ITT) using last observation carried forward method for imputation. Patients completing follow-up and assessments at least up to 6 week following initiation of the therapy were included in ITT analysis. Descriptive statistics was calculated. Normality of data was tested using Shapiro-wilk test. Chi Square test was used to compare categorical variables across groups. To compare continuous variables across groups that were normally distributed, paired t test and independent sample t test were applied. Man-Whitney U test was done to compare continuous variables not having normal distribution (CGI-I).
A mixed ANOVA with Bonferroni correction was used to compare improvement in IRLS score over the study period. Age, duration of illness, family history of illness and serum ferritin at baseline were taken as co-variates. While comparing the change in RLS severity across seven timepoints of measurements, test of sphericity could not be met in the sample; hence Greenhouse-Geiser corrected degrees of freedom were used while interpreting the results. Levene's test depicted a homogenous variance.
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7

Lumbar Lordosis and Patient-Reported Outcomes

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Descriptive statistics for continuous variables are presented as means with standard deviations, and categorical data are presented as numbers and percentages. The total cohort was divided into quintiles based on the preoperative LL and analyzed in relation to changes in PROMs 2 years after surgery. The mean changes in PROMs, ODI, ZCQ, GPE, and NRS for back and leg pain are presented with means with a 95% confidence interval (CI). At baseline, groups were compared using the ANOVA test for continuous variables and the Chi-square test for categorical variables. The quintiles were compared with a likelihood ratio test in relation to changes in PROMs 2 years after surgery. The changes in proms 2 years after surgery in relation to quintiles of lumbar lordosis were adjusted for respective baseline PROMs and for age, sex, smoking, BMI, Schizas score, and Pfirrmann score. Multiple regressions were also used to analyze the association between baseline parameters and clinical outcomes 2 years after surgery. The variables in the regression model were baseline PROMS, age, sex, BMI, Schizas score, and Pfirrmann score. A p < 0.05 was significant. We used SPSS (IBM SPSS Statistics for Mac, Version 26.0, Armonk, NY: IBM Corp. USA) for statistical analyses.
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8

Comparative Analysis of Research Articles

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Statistical analysis was completed using IBM SPSS Statistics for Mac, version 25.0, released 2017 (Armonk, NY: IBM Corp). Content analysis using the 25-question assessment and the DISCERN instrument was performed by treating the data as ordinal variables and analyzing with the Kruskal–Wallis test. A post-hoc Dunn-Bonferroni test was used to determine pairwise comparisons. Statistical significance was set at P≤0.05 for the main comparisons and the pairwise comparisons. The readability analysis was conducted using a Kruskal–Wallis test to compare the mean reading grade level for each article. A post-hoc Dunn-Bonferroni test was used to determine pairwise comparisons. A Spearman correlation test was carried out to evaluate correlation between accuracy and readability. Statistical significance was set at P≤0.05 for the main comparisons, Spearman correlation, and pairwise comparisons.
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9

Statistical Analysis of Biomarker Associations

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SPSS Statistics for Mac (version 17; SPSS, Inc., Chicago, IL, USA) was used for statistical analysis. Interdependence between immunostaining and FISH results as well as clinical data was calculated using the Chi-squared and Fisher's exact tests and displayed by cross-tables. Group differences were examined using the t-test. Survival curves were plotted using the Kaplan-Meier method and analyzed using the log-rank test. Univariate and multi-variate analyses were performed for prognostic factors of recurrence-free and overall survival using the Cox regression model. All tests were two-sided. P<0.05 was considered to indicate a statistically significant difference.
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10

Survival Analysis of Biomarker Correlations

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Clinical data were collected prospectively and analyzed according to a standardized protocol as previously described11 (link),12 (link). SPSS Statistics for Mac (Version 21, SPSS) was used for statistical analysis. Interdependence between stainings and clinical data were calculated using the chi-squared and Fisher’s exact tests, and displayed by cross-tables. Survival curves were plotted using the Kaplan–Meier method and analyzed using the log-rank test. All tests were two-sided. P values < 0.05 were considered statistically significant.
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