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Sas 9.1 statistical

Manufactured by SAS Institute
Sourced in United States

SAS 9.1 is a statistical software package developed by SAS Institute. It provides a suite of tools for data management, analysis, and reporting. The core function of SAS 9.1 is to enable users to perform statistical analysis and modeling on a wide range of data types.

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4 protocols using sas 9.1 statistical

1

Repeated Experimental Analysis

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All of the experiments were repeated three times and the results of parallel experiments were averaged; the one-way analysis of variance method was used to analyze whether the data of each group were significantly different from each other at P < 0.05 level (SAS 9.1 statistical software).
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2

Effect of Treatment and Storage on Samples

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One way and two way analysis of variance techniques were used to find out the effect of treatment, storage and their interaction. Duncan Multiple Range Test was used to denote the significant difference among the treatments on SAS 9.1 statistical software. Results were declared significant al p-value 0.05 (P ≤ 0.05) [23 ].
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3

Randomized Dietary Effects and Covariate Analysis

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The experiment was conducted in a completely randomized design with four treatments and five replicates per treatment. The statistical model is represented by the Eq. (5): Yi=μ+αi+βXi-X¯+δij, where Yi was the observed dependent variable, μ was the overall mean, αi was the effect of the diet, β was the regression coefficient or functional relationship with the covariate, Xi the observed value of the covariate applied to the experimental unit, X¯ the mean of the covariate and δij was the random error.
The data were subjected to analysis of variance through the PROC GLM command of the SAS statistical package (SAS version 9.1 2003), and the means were subjected to regression analysis through the PROC REG command of the SAS® (9.1) statistical package (SAS University Edition). The initial weight was used in the statistical model as a covariate when significant. Analysis of ingestive behaviour also included a t-test to verify the effect of the period (daytime and night-time). Significance was declared when P ≤ 0.05.
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4

Polyamine Inhibition Reduces Rectal Putrescine

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The primary endpoint was percent reduction in rectal mucosa tissue putrescine levels from baseline to end of study. In prior research involving either colorectal adenoma patients [23 (link)] or experimental murine models [18 (link)], intestinal tissue putrescine reductions after polyamine-inhibitory treatments (DFMO, or celecoxib) ranged from 67–74%. Sample size calculations posited that percent reduction in putrescine would be 30% under the null and 60% under the alternative hypotheses, yielding a requirement for 20 subjects, using a 2-sided test (alpha = 0.05, power = 80%); 24 patients were enrolled to allow for at least 15% attrition. The Sign Rank test was used to compare baseline to end-of-study rectal tissue putrescine levels, as well as levels of spermidine and spermine. All statistical analyses were conducted using SAS 9.1 statistical software (SAS Inc., Cary, NC, USA).
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