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Sas 9.4 ts level 1m5

Manufactured by SAS Institute
Sourced in United States

SAS 9.4 TS Level 1M5 is a software product developed by SAS Institute. It is a maintenance release that provides updates and enhancements to the core SAS 9.4 platform. The software is designed to improve the performance, stability, and functionality of the SAS environment.

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Lab products found in correlation

11 protocols using sas 9.4 ts level 1m5

1

Multivariate Analysis of Experimental Data

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We performed an analysis of variance (ANOVA) and Duncan’s Multiple Range Test (DMRT) using SAS9.4 TS Level 1 M5 (Ver.1.0.19041; SAS Institute Inc., Cary, NC, United States). We used the package corrplot in R version 1.2.5033 to conduct correlation analysis [56 (link)].
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2

Cataract Treatment Outcomes in Polish Seniors

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Continuous variables are presented as means with standard deviations or medians with interquartile ranges. Differences between the groups were verified with the Student’s t-test or the Mann–Whitney U-test. Categorical data is presented as counts and percentages. The chi-square test or Fisher’s exact test was used to compare the groups. The logistic regression method was applied to assess the relationship between cataract treatment and the set of independent variables. Additional models analysed interaction to assess changes over time, i.e., between the PolSenior and PolSenior2 cohorts. Multivariate models were developed using the backward stepwise procedure, including only cases with a complete set of data. Regression coefficients were used to calculate odds ratios (ORs) with 95% confidence intervals (95% CI). Statistical results were considered significant at p ≤ 0.05.
The results in Tables 2, 3 are presented after the weighting procedures for the Polish population as percentage or mean values with 95% CI. A statistically significant difference between the groups was assumed for non-overlapping confidence intervals. Statistical packages R (R Core Team, version 3.6.3) and SAS 9.4 TS Level 1 M5 were used for the analysis.
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3

Diagnostic Outcome Comparison Protocol

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To compare the diagnostic outcome, the Kappa value and observer agreement were calculated using SAS 9.4 TS Level 1M5 by SAS Institute Inc., Cary, NC, USA.
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4

Socioeconomic Factors in Smoking Cessation

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To compare socioeconomic factors for cases and controls on the redemption of prescriptions, we used a conditional logistic regression model with case = 1, control = 0. We corrected for socioeconomic factors using Statistics Denmark model Socio13.39 Statistical analysis was performed using SAS 9.4 TS Level 1M5 (SAS, Inc., Cary, NC, USA).
An attempt to quit smoking was defined as the redemption of a prescription for smoking cessation medication in the period between 2009 and 2015. Subsequent attempts were defined as redemption of a prescription for smoking cessation medication more than six months after redeeming the previous prescription, plus the defined daily dosage (DDD) of the previously redeemed prescriptions.
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5

Statistical Analysis of Experimental Data

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We performed the t-test and correlation analysis using SAS 9.4 TS Level 1M5 (Ver.1.0.19041; SAS Institute Inc., Cary, NC, United States).
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6

Gender Differences in Healthcare Costs

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Costs are presented as annual means for cases and controls. Statistical significance of the cost estimates and DCCI was assessed by non‐parametric bootstrap analysis. A significance level of 0.05 was assumed for all tests. In the before and after analysis, only cases with at least a 5‐year follow‐up period prior to diagnosis were included. A Generalized Estimating Equation (two‐step model) for gamma regression was used to compare healthcare costs, income from employment and public transfer income in female cases and controls with male cases and controls within age groups and to assess gender differences in healthcare costs (adjusted for age). The two‐step model takes individuals with no costs or income (= 0) into account. Statistical analyses were performed using SAS 9.4 TS Level 1M5 (SAS, Inc., Cary, NC, USA).
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7

Statistical Analysis of Complex Survey Data

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The data management and the statistical analyses were performed with R version 3.6.3 R (R Core Team, version 3.6.3) and SAS 9.4 TS Level 1M5 (SAS Institute Inc., Cary, NC, USA). The continuous variables were compared with t-tests or Mann–Whitney U tests for two groups and in the case of three or more groups, ANOVA or Kruskal–Wallis tests were used for normally and non-normally distributed variables, respectively. The proportions were compared with chi-square test. Sampling weights were included in statistical calculations to account for the complex survey design using R survey package. The post-stratification procedure was used to match age–sex sample distribution to the population of Poland. The two-tailed tests were carried out with significance level of p ≤ 0.05.
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8

Sarcoidosis and Antidepressant Discontinuation

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Cases and matched comparators were followed until A/D, death, migration, or end of follow-up in 2018, whichever came first. Baseline characteristics were presented as proportion, except age, which was summarised as a mean with standard deviation (SD). Differences in SES and DCCI between cases and matched comparators were estimated using the Chi2 test. The cumulative incidence of A/D was estimated starting on the day of inclusion using a Cumulative Incidence Function (CIF), which takes death into account as a competing risk. Cumulative incidence curves were plotted to describe the incidence of A/D over time. We used the Fine-Gray subdistribution hazard regression model (28 (link)) to estimate the association between sarcoidosis and A/D. The subdistribution hazard ratio (sHR) for A/D was adjusted for DCCI and SES. DCCI was treated as a categorical variable of three groups: 0, 1-2, and >2 points. We performed a sensitivity analysis estimating the sHR for A/D where cases and comparators who only redeemed one prescription of antidepressants within one year were included in the cohorts. The cumulative incidence and sHR were stratified by age-group (18-29, 30-39, 40-49, 50-59 and ≥60 years) and gender. We used 95% confidence intervals (95% CI) and a significance level of 0.05. Statistical software: SAS 9.4 TS Level 1M5 (SAS, Inc., Cary, NC, USA).
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9

Proportions of Patients in ICS Treatment

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We calculated the proportion of patients in each ICS treatment group for each year of study. We also calculated the proportion of patients in each group of age (40–49 years, 50–59 years, 60–69 years, 70–79 years, or 80+ years), sex (male or female), CCI (0, 1, 2, or 3+), co-habitation status (living alone or co-habiting), education (primary, secondary, vocational, or college), and income status (employed, unemployed, disability pension, early retirement, age pension, education, or other). For age, we also calculated the mean and standard deviation. All analyses were performed using SAS 9.4 TS Level 1M5 (SAS, Inc., Cary, NC, USA).
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10

Antibiotic Resistance Mechanisms Evaluation

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Data were analyzed for statistical significance by a completely randomized design with 2 × 3 factorial structure (QAC-adapted and non-adapted stress vs. three methods of sublethal adaptation) in a randomized complete block design with replication considered as block. Significant differences in MIC of trimethoprim and the lag phase duration at OD600 between QAC-adapted subpopulations and non-adapted control were analyzed with the unpaired two-tailed t-test at three significance levels (p < 0.05; p < 0.01; and p < 0.001) using Microsoft Excel (Microsoft Excel, Version 2008). The fold increase and percentage increase in MIC of trimethoprim and fold increase in growth rate (OD600) were obtained using Duncan’s multiple range test (p < 0.05). Statistical analysis was performed using one-way ANOVA at significance level of p < 0.05. Logs transformed counts for survivals were analyzed using One-way ANOVA in a completely randomized block design and means were separated by Fisher’s protected LSD when p < 0.05. The statistical analysis was in this study was performed using the SAS software (SAS 9.4 TS Level 1M5; SAS Institute Inc., Cary, NC, USA).
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