Performs Delta Ct (dCt) analysis of the data from a 1-, 2-, or 3-factor experiment. Per-gene statistical grouping is performed for all treatment combinations.
ANOVA_DCt(
x,
numOfFactors,
numberOfrefGenes,
block = NULL,
alpha = 0.05,
p.adj = "none",
analyseAllTarget = TRUE,
set_missing_target_Ct_to_40 = FALSE
)An object containing expression tables, lm/lmer models, ANOVA tables, residuals, and raw data for each gene:
relativeExpressiondCt expression table for all treatment combinations along with per-gene statistical grouping
perGeneNested list containing detailed results for each target gene:
ANOVA_table: Full factorial ANOVA table
lm: lm/lmer model for factorial design
Final_data: Processed data with wDCt values
resid(object$perGene$gene_name$lm): Residuals
The input data frame containing experimental design columns, target gene E/Ct column pairs, and reference gene E/Ct column pairs. Reference gene columns must be located at the end of the data frame. See "Input data structure" in vignettes for details about data structure.
Integer. Number of experimental factor columns
(excluding rep and optional block).
Integer. Number of reference genes. Each reference gene must be represented by two columns (E and Ct).
Character. Block column name or NULL. When a qPCR experiment
is done in multiple qPCR plates, variation resulting from the plates may
interfere with the actual amount of gene expression. One solution is to
conduct each plate as a randomized block so that at least one replicate of
each treatment and control is present on a plate. Block effect is usually
considered as random and its interaction with any main effect is not considered.
Statistical level for comparisons (default: 0.05).
Method for p-value adjustment. See p.adjust.
Logical or character. If TRUE (default), all
detected target genes are analysed. Alternatively, a character vector
specifying the names (names of their Efficiency columns) of target genes
to be analysed.
If TRUE, missing target gene Ct values become 40; if FALSE (default), they become NA.
The function performs ANOVA analysis on weighted delta Ct (wDCt) values and returns variance components along with an expression table containing:
gene: Name of target genes
Factor columns: Experimental design factors
dCt: Mean weighted delta Ct for each treatment combination
RE: Relative expression = 2^-dCt
log2FC: log2 of relative expression
LCL: 95% lower confidence level
UCL: 95% upper confidence level
se: Standard error of the mean calculated from wDCt values
Lower.se.RE: Lower limit error bar for RE (2^(log2(RE) - se))
Upper.se.RE: Upper limit error bar for RE (2^(log2(RE) + se))
Lower.se.log2FC: Lower limit error bar for log2 RE
Upper.se.log2FC: Upper limit error bar for log2 RE
sig: Per-gene significance grouping letters
result <- ANOVA_DCt(data_2factorBlock3ref, numOfFactors = 2, numberOfrefGenes = 3,
block = "block")
result <- ANOVA_DCt(data_repeated_measure_2, numOfFactors = 2, numberOfrefGenes = 1,
block = NULL)
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