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Spss 26.0 statistical

Manufactured by IBM
Sourced in United States

SPSS 26.0 is a statistical software package designed for data analysis and management. It provides a range of analytical tools and capabilities for conducting various statistical tests, including regression analysis, hypothesis testing, and data modeling. SPSS 26.0 is intended to assist users in processing and analyzing data from a variety of sources.

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93 protocols using spss 26.0 statistical

1

Perceptions of Special-Needs Patients

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The data were entered into Microsoft Excel 2010 and processed using the IBM SPSS 26.0 statistical software (IBM Corp., Armonk, NY, USA). Descriptive analyses, including percentages, means, and standard deviations, were used to describe the characteristics of the study participants. When the data distribution was not normal, a Mann–Whitney test was performed to assess differences in participants’ perceptions of special-needs patients (study program and clinical-student experience in caring for patients with special needs). Chi-square analysis was used to assess the relationship between the study program and clinical-student experience in caring for special-needs patients on the outcome survey on the perception of and the training program for SCD. The level of statistical significance for all the tests was set at p < 0.05 with a confidence interval of 95%.
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2

Evaluation of Experimental Conditions

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All the experiments were performed in triplicate, and the data were expressed as mean ± standard deviation. ANOVA was performed with Duncan’s multiple range tests by SPSS 26.0 statistical software (IBM, NY, United States). p < 0.05 indicated a significant difference among groups.
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3

Statistical Analysis of Intervention Efficacy

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We used SPSS 26.0 statistical software (SPSS software Inc, IBM Corp, Armonk, New York, USA) to analyze the data by Student’s t-test and one-way ANOVA (LSD or Tamnheini tests) when appropriate. The results were exhibited as the mean ± SD. Paired t-test was used for the urine protein of mice before and after drug intervention. To examine the ranking data, we used the rank sum test. P < 0.05 indicated a statistically significant difference.
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4

Evaluating mCTA for Differential Diagnosis of ID

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The agreement of the 2 post-processors image quality and interobserver were determined by calculation of kappa (K) values. The strength of agreement was rated as follows: 0= poor, 0–0.20= slight, 0.21–0.40= fair, 0.41–0.60= moderate, 0.61–0.80= substantial, and 0.81–1.00= almost perfect (11 (link)). Sensitivity, specificity, accuracy, and positive predictive value (PPV) and negative predictive value (NPV) of mCTA for differential diagnosis of ID were calculated using the consensus DSA evaluation as the reference standard. The net reclassification index (NRI) (12 (link)) was used to evaluate the differential efficacy of mCTA and sCTA. Mean and standard deviation (SD) were used to describe quantitative variables, whereas in the case of qualitative variables, percentages were used. First, a bivariate analysis was carried out, using Student’s t-test for independent samples or Mann-Whitney U-test for quantitative variables, whereas the chi-square test was used for qualitative variables. Wilcoxon matched-pairs signed-rank test and Fisher’s exact probability test were used to examine the ability of different images to distinguish between ID and IA. A P value <0.05 was considered statistically significant. All statistical analyses were performed using the SPSS 26.0 statistical software package (IBM Corp, Armonk, NY, USA).
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5

Vaginal Contractility Assessment Protocol

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Sample sizes were calculated using previously published data in which the contractile function of the nonhuman primate vagina following the implantation of Restorelle and UltraPro (Ethicon, Somerville, NJ, USA) was compared to Sham [17 (link)]. Based on that data, eight animals per group would be needed to detect differences between Sham, PP, and PDMS in the contractile function (primary endpoint) with a power of 85% using a one-way ANOVA with a two-sided significance level of 0.05. Kolmogorov-Smirnov tests were utilized to assess the normality of the data. Normally distributed data is represented as mean ± standard deviation and non-normally distributed data is represented as median (interquartile range). One-way ANOVA with Gabriel’s post-hoc testing was utilized to compare the contractile response to 120 mM KCl, total collagen content, and sGAG between groups while smooth muscle thickness was compared between groups using Kruskal-Wallis tests followed by Mann-Whitney tests with a Bonferroni correction when appropriate. Mann-Whitney tests were used to compare the percent of red, orange, yellow, and green fibers and the red to green ratio. All statistical analyses were performed using SPSS 26.0 statistical software (IBM, Armonk, NY, USA).
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6

Statistical Analysis of Categorical and Continuous Variables

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Excel 2016 for Windows (Microsoft Corporation, Seattle, WA, USA) and SPSS 26.0
statistical software for Windows (IBM Corp., Armonk, NY, USA) were used for the
statistical analysis. Categorical variables are expressed as frequency.
Continuous variables are expressed as mean ± standard deviation. Student’s t
test and the chi-square test were used. A P value of <0.05 was considered
statistically significant.
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7

Rooting Efficiency Analysis Protocol

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Rooting efficiency date were analyzed using the t-test by the SPSS 26.0 statistical software (IBM Corp. Armonk, NY, USA). Triplicate measurements were averaged and included the standard error (±SE).
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8

Candida Invasive Infections: Epidemiology

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After data collection, SPSS 26.0 statistical software (IBM Corp., Armonk, NY, USA) was used for data analysis, and data analysis was performed from August 2023 to December 2023. Counting data including GA at birth and BW are expressed as median and quartile (Q1, Q3). Categorical data including Candida species distribution, risk factors and therapeutic outcomes are presented as frequencies and percentages, and differences between the EOD group and NEOD group were tested by chi-square test, with P < 0.05 as the difference having statistical significance, and all P values were 2-sided.
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9

STFT Colon Polyp Detection Model

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The data were analyzed and processed using SPSS 26.0 statistical software (IBM Corp.). The main evaluation indicators of the STFT colon polyp detection model is accuracy, precision, recall, and F1-score (also known as balanced F score). The performance of the STFT detection model in image and video testing is evaluated by calculating the receiver operating characteristic curve (ROC) and the area under the ROC curve (AUC) to obtain the best threshold. Apart from AUC, other indicators are calculated using true positive (TP), true negative (TN), false positive (FP), and false negative (FN) (refer to supplementary materials for formulas). The comparison between the STFT polyp detection model and endoscopists is conducted using the chi-square test, and accuracy, sensitivity, specificity, positive predictive value, and negative predictive value are calculated. P value < 0.05 indicates a statistically significant difference.
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10

Multivariate Analysis of Gram-negative and CRO Infections

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The SPSS 26.0 statistical software package (IBM SPSS Statistics, IBM Corporation, Armonk, NY, USA) was used for statistical analysis of data. Continuous variables were expressed as mean ± standard deviation or median (interquartile range [IQR]), and classified data were expressed as a percentage. Pearson’s chi-square test or Fisher's exact test was used for univariate comparisons of differences between two groups. Variables with P < 0.05 in univariate analysis were introduced into the final multivariate model. Multivariate logistic regression was applied for multivariate analysis based on forward stepwise logistic regression. Odds ratio (OR) values and 95% confidence intervals (95%CI) were used to describe the independent factors associated with Gram-negative and CRO infections. When P < 0.05 in the two-tailed test, the difference was considered to be statistically significant.
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