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Stata se 11

Manufactured by StataCorp
Sourced in United States

STATA/SE 11.0 is a statistical software package developed by StataCorp. It provides a comprehensive set of tools for data analysis, modeling, and visualization. The software is designed to handle a wide range of data types and supports advanced statistical techniques, including regression analysis, time-series analysis, and multivariate methods.

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137 protocols using stata se 11

1

Cytokine Profiling in Controlled Ovarian Hyperstimulation

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Chi-squared, independent samples t-tests, or Mann-Whitney U tests were used to compare MNC and COH patient demographics, cycle details, FF, and plasma cytokines following tests for normal distribution by Shapiro-Wilk test (Stata/SE 11.1, Texas, USA). In order to address the interrelationships between multiple cytokines and the impact that COH has upon these, heat maps were generated using R 2.7.0 software (R Foundation for Statistical Computing, Vienna, Austria). Correlations between the different cytokines were determined for MNC and COH data using Kendall's tau as a measure of correlation (Stata/SE 11.1). Resulting P values were adjusted for multiple comparisons with Holm's correction (P < 0.05 was considered significant).
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2

Meta-Analysis of Cell-free DNA

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The data analyses were performed using Stata/SE 11.0 software. The aggregated data of HRs and 95% CIs were analyzed using inverse-variance weighting. According to the level of cfDNA, the patients were divided into two groups to compare the OS. A Chi-squared-based Q statistic and inconsistency index (I2) statistic were used to examine heterogeneity. A P-value of <0.1 and I2 value of >50% indicated significant heterogeneity. A random-effects model was used if heterogeneity was significant; otherwise, the fixed-effects model was applied. If heterogeneity was significant, sensitivity analyses were conducted by deleting each study individually to evaluate the quality and consistency of the results, and subgroup analyses were conducted for TNM stage and treatment history. Publication bias was evaluated using Funnel plots and Begg's tests. Probable significant publication bias was considered for P-values <0.05. All the tests were performed using Stata/SE 11 software.
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3

Statistical Analysis of Continuous and Categorical Variables

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Stata/SE 11.1 (College Station, Texas) was used to perform all statistical analysis. A two-sided p value of less than 0.05 was considered statistically significant. The Student’s t-test was used to analyze continuous variables. These variables were reported as a mean ± standard deviation if normally distributed or as a median and range if skewed. The chi-squared test was used to analyze categorical variables. These variables were reported as a proportion (%) of the overall cohort.
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4

Evaluating PET Imaging Biomarkers

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Statistical evaluation was performed with Stata/SE 11.1 (StataCorp, College Station, TX, USA) using the descriptive statistics and box plots. Linear discriminant analysis was performed for calculating the sensitivity, specificity, positive predictive value (PPV), negative predictive value (NPV) and highest accuracy. The 2-sided Wilcoxon rank sum test was applied for all PET parameters, which also included SUV, using a single parameter analysis to assess groups. The significance level was set to p<0.05.
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5

Intravitreous Injection Retinal Analysis

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For statistical analysis, we tabulated the data into a Microsoft ® Office Excel ® 2007 spreadsheet. The spreadsheet was imported for analysis using the Stata/SE 11.1 software for Windows.
We used the paired t test in the majority of cases, and the Wilcoxon signed-rank test when the variance difference between samples was large. A p value of 0.05 was considered to indicate a statistically significant change in the retina after the intravitreous injection.
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6

Statistical Analysis of Sample Characteristics

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Sample characteristics were summarized using descriptive statistics. Where relevant exact McNemar, Fischer tests and chi-squared test were performed using IBM SPSS Statistics 21.0 and Stata/SE 11.1 (StataCorp LP, College Station, TX, USA) statistical softwares. The cut-off for statistical significance was set at p < 0.05.
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7

Evaluating Statewide Health Campaigns

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Data were analysed using Stata SE 11.1 (StataCorp, Texas) during 2013 and weighted to the population on sex, age, place of residence [66 ] and educational attainment [67 ]. Chi-square analysis assessed whether demographic characteristics differed between states at each survey. Logistic regression analysis tested interactions by state (WA versus Victoria) and subsequent surveys (baseline versus W1; baseline versus W2) controlling for socio-economic status (SES) and BMI. Interactions were tested for the full sample and the sub-sample of overweight/obese respondents. Overweight/obese and healthy weight/underweight categories were combined and are referred to as ‘overweight’ and ‘not overweight’, respectively. Logistic regression was undertaken to determine whether campaign recall differed according to sex, age, BMI, parental status, place of residence and SES when controlling for all other factors and time spent viewing commercial television. Differences in ratings of perceived effectiveness by ad type (principal versus supplementary) were tested using logistic regression controlling for individual-level clustering and the above demographics.
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8

Survival Analysis of Liver Disease

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The data analysis and statistical software, Stata/SE 11.1 (College Station, Texas, USA), was used to perform all analysis. Statistical significance was defined as a two-tailed p value of <0.05. The Student's t-test was used to analyse continuous variables. These variables were reported as a mean±SD if normally distributed or as a median and range if skewed. The χ2 test was used to analyse categorical variables. These variables were reported as a proportion (%) of the overall cohort.
The Kaplan–Meier method was used to approximate the overall survival, and the significance of survival differences between the sexes was determined using the log-rank test. Differences in survival among men and women within different diagnosis scenarios and aetiologies, including hepatitis B, hepatitis C, and non-viral diseases were also evaluated using the Kaplan-Meier method and log-rank test. A stepwise multivariate Cox proportional regression was used to estimate HRs with a 95% CI, which related patient survival to baseline predictors that were found to have a significant effect on survival during univariate analysis.
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9

Fever Severity and Skin Biomarkers

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Each criterion was rated from 0 to 10 (0 to 6 for the faces). Feverish children were divided into 3 groups based on the severity of fever (38° to 38.5°C, 38.6°C to 39°C, 39.1°C and above) to study the relationship between SB and severity of fever. Data were entered by the software 4D (v2004) and analyzed using Stata SE 11.1 (Stata Corp., College Station, TX, USA). The Pearson chi-square test was used for univariate analyses and logistic regression for multivariate analysis.
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10

Survival Analysis of Clinical Outcomes

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Statistical analyses were performed using the SPSS (SPSS, Inc., Chicago, IL, USA) and STATA (STATA Corp., College Station, TX, USA) software packages (SPSS for Windows, version 18.0.1 and STATA/SE 11.1). Differences in the means of continuous variables were analysed using non-parametric tests (Mann–Whitney or Kruskal–Wallis) for two and multiple independent samples, respectively. Univariate survival analysis for the outcome measure (disease-specific survival [DSS] or disease-free survival [DFS]) was based on the Kaplan–Meier method, with log-rank (Mantel–Cox) comparison test. DSS and DFS were calculated, based on the time from diagnosis to death (due to disease), and on the time from diagnosis to the appearance of metastatic disease, respectively. In all tests, the values p < 0.05 were regarded statistically significant.
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