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General linear model procedure

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The General Linear Model (GLM) procedure in SAS Institute's lab equipment offers a comprehensive approach to analyzing linear models. It provides the core functionality to fit and evaluate a wide range of linear models, including regression, analysis of variance (ANOVA), and analysis of covariance (ANCOVA). The GLM procedure handles both continuous and categorical independent variables, allowing for flexible model specification and hypothesis testing.

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14 protocols using general linear model procedure

1

Assessing Effects of SID Lys:Thr Ratios

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Data were analyzed as a completely randomized-block design using the general linear model procedures (SAS Institute Inc., Cary, NC, USA). The pen served as the experimental unit for all response criteria except meat quality wherein individual pigs were the experimental unit. Variability in data is expressed as standard errors of the mean. Linear and quadratic polynomial contrasts were performed to determine the effects of the different SID Lys:Thr ratios in the diet, with p<0.05 indicating significance and p<0.10 indicating trends.
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2

Effects of Protected Organic Acid Blends

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All data were subjected to statistical analysis in a randomized complete block design using the general linear model procedures (SAS Inst. Inc., Cary, NC, USA), with the pen serving as the experimental unit. The initial BW was used as a covariate for the ADFI and ADG, and the initial values were used as a covariate for the blood profile. Before conducting statistical analysis of the microbial counts, the value was transformed logarithmically. Linear and quadratic polynomial contrasts were performed to determine the effects of inclusion level of 0.1% and 0.2% of protected organic acid blends in the diet.
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3

Analysis of Axonal Length and Colocalization

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The results of axonal length were analyzed in a completely randomized design using the general linear model procedure (SAS Institute Inc., Cary, NC) with the significance level set at P ≤ 0.05. Least square means ± s.e.m. were used to analyze differences between treatments (Figure 8). The results of axon colocalization (Figure 6) were analyzed by a frequencies procedure, the Pearson correlation coefficient was used (SAS Institute Inc., Cary, NC).
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4

Chemical Composition of Ensiled TMR

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Analyses were performed using the general linear model procedure (SAS Institute, Cary, NC, USA). Data on Chemical composition and characteristics data of fresh and ensiled TMR were subjected to one-way analysis of variance (ANOVA) with treatment as factor. In aerobic conditions, the data on chemical composition of silages were 4 (treatments)×4 (deterioration periods)×3 (replicates) = 48 observations corresponding to each variable and were analyzed in a repeated measures analysis of variance using the PROC GLM. In General Linear Model, seven various covariance structures (CS, UN, HF, AR, ARH, ANTE) were applied. AIC and AICC criteria were used to determine the most appropriate covariance pattern for fitting data, it was determined that unstructured (UN) covariance structure gave the best fit to data set. The triplicate samples were considered as replicates, and treatments and deterioration periods were considered to be between- and within-subjects factor, respectively. All unstructured covariance matrix of the data were meet the assumption of sphericity. Statistical difference between means was determined by Tukey’s multiple comparison. Differences were considered significant when probability was less than 0.05.
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5

Starch Source and Aging Effects on Meat Quality

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The data were considered as a 3 × 2 factorial arrangement in a completely randomised design, with 3 starch sources (CO, CA, and PI) and 2 ageing periods (14 and 21 days post-mortem). The general linear model procedure (SAS Institute Inc., Cary, NC, USA) was used for analysis of variance to analyse meat quality, texture profile, and ribonucleotide content, including the effects of starch source, ageing period, and their interaction. For fatty acid composition, only starch source was defined as a treatment. The PDIFF option was used to separate least square means. P values less than 0.05 were considered statistically significant. Principal component analysis (PCA) was used to evaluate the relationship between ribonucleotide content and fatty acid composition in relation to the different starch sources and ageing period using XLSTAT software (Addinsoft, Long Island City, NY, USA).
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6

Multifactorial Analysis of Forage Degradability

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Chemical composition data were analysed in a randomized complete block design with 5 replications arranged in a 2 × 3 factorial using software package of SAS Institute Inc., (2003) , version 9.1.3. In vitro and in sacco degradability data were analysed using the NEWAY computer programme for estimation of degradation constants (Osuji et al., 1993 ). The analysis of variance was carried out on the chemical constituencies and on DM disappearance coefficients a, b, c, a + b and P of ICEAP 00557, ICEAP 01514 and CIMMYT 100/01 using the SAS program General Linear Model Procedure (SAS Institute Inc, 2003 ). Differences between treatment means were assessed by Least Significant Difference. The following model was used:
Yijkl=μ+Ti+Vj+Dk+(VDT)ijk+Eijkl where Yijkl = observation of the dependent variable; μ = fixed effect of population mean for the variable; Ti = effect of incubation time h (0, 4, 8, 12, 24, 30, 48); Vj = effect of variety (j = 3; ICEAP 00557, ICEAP 01514 and CIMMYT 100/01); Dk = effect of drying method (k = Oven-drying and shade-drying); VDTijk = effect of interaction among variety at level j, drying method at level k and incubation time at level l; Eijk = the random error associated with observation ijkl.
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7

Dietary BPM Concentration Effects

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All data were statistically analyzed using the General Linear Model procedure (SAS Inst. Inc., Cary, NC, USA) in a randomized completely block design. The replicate cage was used as the experimental unit. Orthogonal contrasts were used to examine the linear and quadratic effects in response to the increase of dietary BPM concentrations. Variability in the data was expressed as the standard error of means (SEM), P < 0.05 was considered statistically significant.
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8

Evaluating Nutrient Digestibility in Pigs

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Outliers were tested using the UNIVARIATE procedure (SAS Inst. Inc., Cary, NC, USA). In Exp. 1, the data for the ATTD of GE and the DE and ME content were analyzed as a completely randomized design using the general linear model procedure (SAS Inst. Inc., USA), with pig as the experimental unit. In Exp. 2, data were analyzed using the MIXED procedure (SAS Inst. Inc., USA). The statistical model for the digestibility values had diet as a fixed effect and period and pig as random effects. Multiple comparisons were conducted using Tukey’s method. In all analyses, the differences were considered significant if p<0.05.
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9

Phytase Supplementation Effects

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All data were statistically analyzed using the General Linear Model procedure (SAS Inst. Inc., Cary, NC, USA) in a randomized completely block design. The replicate cage was used as the experimental unit. Orthogonal contrasts were used to examine the linear and quadratic effects in response to increasing the dietary supplementation of phytase. Variability in the data was expressed as the standard error of means, p<0.05 was considered statistically significant.
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10

Dietary Supplementation of QS

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All data were subjected to statistical analysis in a randomized complete block design using the General Linear Model procedure (SAS Inst. Inc., Cary, NC, USA). The replicate cage was used as the experimental unit. Orthogonal contrasts were used to examine the linear and quadratic effects in response to increasing the dietary supplementation of QS. Variability in the data was expressed as the standard error of means, p<0.05 is considered statistically significant.
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