Description Usage Arguments Details Value Examples
Generate formatted results file from result objects returned by limma, DESeq2, and edgeR pipelines
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| y | Expression data frame the model was run on. Default is NULL. See Details for further description. | 
| data.type | Type of data being analyzed ("rnaseq", "microarray", "flow", "metab"). Default is data.type="rnaseq". | 
| method | string denoting modeling method used ("limma","deseq2","edgeR") | 
| object | results object generated from  | 
| lm.Fit | linear model fit object generated from 
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| comp.names | Optional vector of comparison (contrast) names. Default is NULL. | 
| var.symbols | Optional vector of additional annotations for the variables. Otherwise, the rownames of the expression data are used. Default is NULL. | 
| gene.sets | A list of gene sets. Default is NULL. See Details for further description. | 
| annotations | A data frame of additional annotations for the gene sets. Default is NULL. See Details for further description. | 
This function takes results obtained from differential analysis 
pipelines found in limma, DESeq2, or edgeR and formats 
them for the BART app. 
The expression data y and lm.Fit objects are used to obtain 
the residual matrix from the fitted model. These parameters are only needed 
when method = "limma" and data.type = "rnaseq" or "microarray" and can 
otherwise be left as NULL. It is important to remember that y should 
be the expression data used for modeling (e.g. voom transformed data). The 
residual matrix is stored as an element of the returned list and can be 
used in downstream gene set analysis using runQgen (Please 
visit for more details).
The object parameter takes as input model result objects returned by 
functions in limma, DESeq2, or edgeR. When method = "limma", the expected 
input is the single object returned by eBayes since it 
is able to store results across multiple comparisons. When method = 
"deseq2" or "edgeR", the result object(s) returned by 
results, glmLRT, or 
glmQLFTest must be wrapped in a list in which each 
element is an object containing the results for a single comparison. 
The comp.names parameter is a character vector of comparison names 
that is particularly useful when method = "deseq2" or "edgeR" since 
comparison names are not extracted from the result objects generated by 
either of those pipelines. When using limma, the comparison names can also 
be defined in makeContrasts. It is important that the 
names are written in the correct order. For example, if object = list(AvsB, 
CvsD), where AvsB and CvsD are result objects for the comparisons "group A 
vs group B" and "group C vs group D" respectively, then comp.names = 
c("CvsD", "AvsB") would incorrectly assign the name "CvsD" to the 
comparison "group A vs group B" and vice versa. The var.symbols 
parameter is typically used to provide a character vector of gene symbols. 
The vector provided must be the same length and in the same order as the 
row names of the data used for modeling.
The gene.sets parameter is a list in which each element is a 
character vector of gene names comprising a gene set. The gene names must 
match the rownames of the data used for modeling. The gene sets are used to 
create modular maps for each comparison in the DGE section of BART. The 
annotations parameter is a data frame consisting of two columns. The 
first column consists of gene set names and the second column consists of 
additional descriptions for the gene sets.
data.type string denoting the type of data that was analyzed
results the formatted results returned as a data frame
resids data frame of residuals. Returned only if 
data.type="microarray" or "rnaseq" and method="limma". Used to estimate the 
VIFs when running the Qusage algorithm in runQgen.
gene.sets list of gene sets provided by the user. NULL if no 
list provided.
annotations data frame of gene set annotations provided by the
user. Null if no annotations are provided.
| 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 | # Example data
data(tb.expr)
data(tb.design)
# Only use first 100 genes to demonstrate
dat <- tb.expr[1:100,]
# Generate lmFit and eBayes (limma) objects needed for genModelResults
tb.design$Group <- paste(tb.design$clinical_status,tb.design$timepoint,sep = "")
grp <- factor(tb.design$Group)
design2 <- model.matrix(~0+grp)
colnames(design2) <- levels(grp)
dupcor <- limma::duplicateCorrelation(dat, design2, block = tb.design$monkey_id)
fit <- limma::lmFit(dat, design2, block = tb.design$monkey_id, 
             correlation = dupcor$consensus.correlation)
contrasts <- limma::makeContrasts(A_20vsPre = Active20-Active0, A_42vsPre = Active42-Active0, 
                                  levels=design2)
fit2 <- limma::contrasts.fit(fit, contrasts)
fit2 <- limma::eBayes(fit2, trend = FALSE)
# Format results
model.results <- genModelResults(y = dat, data.type = "microarray", object = fit2,
                                 lm.Fit = fit, method = "limma")
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