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Spss 23 statistical software

Manufactured by IBM
Sourced in United States

SPSS 23 is a statistical software package developed by IBM. It provides a comprehensive set of tools for data analysis, including data management, statistical modeling, and visualization. The software is designed to help users analyze and understand complex data sets, with a focus on providing accurate and reliable results.

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Lab products found in correlation

30 protocols using spss 23 statistical software

1

Mortality Prediction from BUN Levels

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The BUN was divided into normal and elevated groups as mentioned before. While analysing BUN in different creatinine, age, and BNP groups, BUN was divided into <30, 30–39, and >40. Creatinine was divided into normal (≤1.5 mg/dL) and elevated (>1.5 mg/dL); age was divided into <80, 80–90, and >90 years; and BNP levels were divided into <400, 400–1999, and >2000 pg/mL.
Using bi‐variable logistic regression, we analysed the relationship between demographic data, BUN, other laboratory results, and overall mortality. All variables with P value < 0.05 were included in the multivariate analysis, using stepwise Cox regression.
We used a multivariate, stepwise logistic regression to identify variables with independent effect on mortality. The goodness of fit of the model was determined by Hosmer–Lemeshow test. The discrimination threshold was classified by area under a curve receiver operating characteristic (AUC ROC).
The correlation between the BUN levels and other laboratory test results was tested by the ordinal‐by‐ordinal Spearman correlation. The same statistical analysis was performed with creatinine and GFR as predictor of all the aforementioned outcomes.
The significance level for testing the statistical hypothesis was determined as P < 0.05. The data processing was done with SPSS statistical software 23, Chicago, Illinois.
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2

Power Analysis for Experimental Design

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We have calculated the minimum sample size necessary for our design based on a previous study [19] . We achieved a power of greater than 80% for detecting the effects that we anticipate at a significance level of P < 0.05 with eight subjects. Data are expressed as means ± SEM. To determine the significance, Student's t test and two-way ANOVA followed by appropriate t-test were used. For correlation studies, Pearson correlation analysis was performed. All calculations were performed with SPSS statistical software (23.0; SPSS, Inc., Chicago, IL). Significance was set as P ≤ 0.05.
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3

Comparative Analysis of Orthopedic Outcomes

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Statistical analyses were performed using SPSS statistical software 23.0 (IBM Corp.). Continuous variables are presented as the mean ± standard deviation and categorical variables were expressed as n (%). The Kolmogorov-Smirnov test was used to check the data for normality of distribution. The t-test was employed to compare variables with a normal distribution. The nonparametric Mann-Whitney U-test was used for variables without a normal distribution, such as the ROM and VAS score. Differences in categorical variables between the two groups were assessed with Fisher's exact test. P<0.05 was considered to indicate statistical significance.
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4

Evaluating Laboratory Indicators for Lung Cancer Risk

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All statistical analyses were performed using IBM SPSS statistical software 23.0 (IBM Corp., Armonk, NY, USA) and GraphPad Prism version 7.00 (GraphPad, La Jolla, CA, USA). The normality of continuous variables was examined with the Kolmogorov–Smirnov test. Continuous variables with a normal distribution are expressed as mean ± standard deviation and were compared by one-way analysis of variance. Skewed continuous variables are presented as median/interquartile range and were assessed by the Kruskal–Wallis H test. Categorical variables are shown as percentages and were analyzed by χ2 tests. Associations between continuous variables were evaluated using Spearman’s correlation analysis. Logistic regression analysis was applied to determine associations between laboratory indicators and lung cancer risk. All tests were two-sided and the significance level was set at P < 0.05.
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5

Molecular Responses of Litchi to Cold Stress

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The IBM SPSS statistical software 23.0 was used to determine significant differences between the treatment and controls. The expression of genes was presented as a heat map diagram using the pheatmap package (http://www.r-project.org/, accessed on 24 June 2022). To explore the relationships between DEGs and the responses of litchi to low temperature, a hypothetical model according to Chen et al. [55 (link)] was specified and analyzed with PLS-SEM with the support of the SmartPLS 2.0 M3 software [56 (link)]. Standardized path coefficient values were generated with the PLS algorithm by the Path Weighting Scheme using a bootstrapping method to obtain the significance of path coefficients. The sign changes were individual changes. The samples during the calculation of the bootstrapping method were 5000, and the ABA-, IAA-, CTK-, JA-, SA-, ETH-, BR-, GA-, SL-related DEGs models were 54, 40, 37, 35, 29, 27, 21, 13, 4, respectively.
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6

Statistical Analysis of Experimental and Control Groups

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The IBM SPSS statistical software 23.0(Chicago, USA) was used for statistical analysis. One-sample Kolmogorov–Smirnov tests were used to evaluate the distribution of variables before test selection. Physical characteristics in the experimental and control groups were compared using the χ2 test for categorical variables (sex, functional level). The Mann–Whitney U test was used to analyze the continuous variable (age). Baseline, post-treatment and follow-up were calculated within groups. A one-way ANOVA test (1 group × 3 tests) was used to compare the differences in assessments between treatment scores within groups at baseline and after 12 weeks and follow-up (24 weeks). When overall significance was found, a pairwise post-hoc test with Bonferroni correction was performed based on an adjusted p-value of 0.017 (0.05/3; dividing p-value to group number). The difference between the groups was determined with two-way repeated-measures mixed ANOVA (2 groups × 3 tests) for normally distributed numerical data. To determine the effect sizes (ES) of the interventions on the measured properties, Cohen’s d formula was applied. The ES was classified as follows: large ES when greater than 0.80, medium ES when 0.50 to 0.80 and small ES when less than 0.50 [27 ].
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7

Biomarker Analysis of lncRNA HOTAIR

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SPSS statistical software 23.0 (IBM Corp. Armonk, NY, USA) was applied for statistical analysis, and GraphPad Prism software 8.2 (GraphPad Software, La Jolla, CA, USA) was utilized to capture images. The difference between groups was compared using Student's paired two-tail t test or Kruskal–Wallis nonparametric test. Classification variables were compared using chi-square test. Spearman correlation analysis was employed to evaluate the correlation of lncRNA HOTAIR with erythrocyte sedimentation rate (ESR), high sensitivity C-reactive protein (hs-CRP), immunoglobulin A (IgA), and other indicators. Data were expressed as mean ± standard deviation or median (quartile range). p < 0.05 was indicative of statistical significance.
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8

Comparative Analysis of MWA and Cryoablation

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All of the data processing was performed with SPSS statistical software 23.0 (IBM Corp.). Measurement and numeration data were analyzed using the χ2 test and unpaired t-test, respectively, to compare the two groups. VAS scores were assessed using a Mann-Whitney test. Fisher's exact test was used when expected number of cases was ≤5. The χ2 or Fisher's exact test was used to analyze the CR, PR, SD and PD of the two groups. Overall survival (OS) rates were estimated according to the life-table method. Kaplan-Meier survival analyses was used to calculate survival curves at 6, 12, 24 and 36 months after MWA and cryoablation. P<0.05 was considered to indicate a statistically significant difference.
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9

Prognostic Biomarkers in NSCLC

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Statistical analysis was performed using R4.1.2 and IBM SPSS statistical software 23.0 to estimate the sensitivity and speci city of TG/HDL-C ratio, non-HDL-C/HDL-C ratio, TC, HDL-C, LDL-C, VLDL-C, Apo-A, and Apo-B. Time-dependent ROC (Receiver operating characteristic) curve was drawn and area under the curve (AUC) was calculated. Time-dependent ROC curves were used to predict all-cause death and thus to calculate TG/HDL-C and non-HDL-C/ HDL-C as a cutoff of continuous variables, which were treated as binary data. Survival analysis was performed using Kaplan-Meier model and Cox proportional risk model to con rm independent prognostic factors for NSCLC. P < 0.05 indicated a statistically signi cant difference.
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10

Retrospective Analysis of Leukemia Outcomes

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Data were analyzed using SPSS statistical software 23.0. Differences in proportions were evaluated by Chi-square test. A value of p < 0.05 was considered to indicate a statistically significant difference. OS was determined based on the time between diagnosis and death or the time of the final clinical evaluation. DFS was defined as the time from CR to relapse or death or last follow-up. The Kaplan–Meier method was used to estimate OS and DFS, and survival curves were compared using the log-rank test. Cox proportional regression was used for the multivariate analysis. Odds ratios were calculated and reported with 95% confidence intervals. CR was confirmed when all the following conditions were fulfilled: less than 5% of blasts in the bone marrow, no leukemic blasts in the peripheral blood or extramedullary sites, and recovery of blood counts.
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