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Sas stat software for windows version 9

Manufactured by SAS Institute
Sourced in United States

SAS/STAT software for Windows version 9.4 is a comprehensive set of statistical analysis tools designed to work within the SAS platform. It provides a wide range of statistical procedures for data analysis, modeling, and forecasting. The software is intended to be used by researchers, statisticians, and data analysts to perform statistical analysis on their data.

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2 protocols using sas stat software for windows version 9

1

Factor Analysis of TC3 Questionnaire

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Factor analysis was used to describe the variability among the TC3 questions in order to identify the underlying structure of the factors of the TC3. Factor analyses were conducted using SAS/STAT software for Windows version 9.4 (SAS Institute, Cary, NC, USA). A polychoric correlation covariance matrix with a varimax rotation was used for the factor analysis; a technique that allows PROC FACTOR in SAS to perform factor analysis on binary and ordinal data (Andrich, 1988 ; Bartholomew, 1987 ; van Rijckevorsal & de Leeuw, 1988). The number of factors in the model was determined based on the scree test plot, which plots the factors on the x-axis versus the corresponding eigenvalues on the y-axis (Colgan, 1981 ). Additionally, at least two variables must have loading scores ≥ .50; factors must have an eigenvalue > 1.0; and each factor must account for at least 1% of the total variance. A factor loading score was calculated for each variable. The factor loading scores represent the correlations between each of the variables included in each factor. Generally, a factor loading score ≥ .30 is considered meaningful. For this analysis, a factor loading score ≥ .50 was used to identify the most highly correlated variables in each factor.
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2

Methionine Kinetics in Swine

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Data were analyzed with SAS/STAT software for Windows, version 9.4 (SAS Institute Inc.). The test for normality was performed by the UNIVARIATE procedure of SAS. The data were analyzed by repeated-measures ANOVAs with the MIXED procedure. The ANOVA models contained the fixed effects of dietary group (Control, LMET, DLMET, DLHMTBA), status (fed, feed-deprived), the interaction group × status, and a random sow effect. Repeated measures on the same animal were considered by the repeated statement of proc MIXED (repeated variable: status) using an unstructured type for the block diagonal residual covariance matrix. Group and status (fed, feed-deprived) differences were analyzed using the Tukey–Kramer test. Statistical significance was considered at P < 0.05. The results are expressed as least square means (LSmeans) ± SEMs. The primary outcomes of the study were Met and Cys quantitative kinetics, liver protein L-MetInc, and liver mRNA abundances. Plasma and liver free AA concentrations and vitamin and metabolite concentrations were secondary outcomes.
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