enrichmentTest | R Documentation |
Perform the Fisher exact test for all the possible 2x2 contingency tables, considering differential abundance direction and enrichment variable.
enrichmentTest(method, enrichmentCol, alternative = "greater")
method |
Output of differential abundance detection method in which
DA information is extracted by the |
enrichmentCol |
name of the column containing information for enrichment analysis. |
alternative |
indicates the alternative hypothesis and must be
one of |
a list of objects:
data
a data.frame
object with DA directions,
statistics, and feature names;
tables
a list of 2x2 contingency tables;
tests
the list of Fisher exact tests' p-values for each
contingency table;
summaries
a list with the first element of each
contingency table and its p-value (for graphical purposes);
extractDA
, addKnowledge
, and
createEnrichment
data("ps_plaque_16S")
data("microbial_metabolism")
# Extract genera from the phyloseq tax_table slot
genera <- phyloseq::tax_table(ps_plaque_16S)[, "GENUS"]
# Genera as rownames of microbial_metabolism data.frame
rownames(microbial_metabolism) <- microbial_metabolism$Genus
# Match OTUs to their metabolism
priorInfo <- data.frame(genera,
"Type" = microbial_metabolism[genera, "Type"])
# Unmatched genera becomes "Unknown"
unknown_metabolism <- is.na(priorInfo$Type)
priorInfo[unknown_metabolism, "Type"] <- "Unknown"
priorInfo$Type <- factor(priorInfo$Type)
# Add a more informative names column
priorInfo[, "newNames"] <- paste0(rownames(priorInfo), priorInfo[, "GENUS"])
# DA Analysis
# Make sure the subject ID variable is a factor
phyloseq::sample_data(ps_plaque_16S)[, "RSID"] <- as.factor(
phyloseq::sample_data(ps_plaque_16S)[["RSID"]])
# Add scaling factors
ps_plaque_16S <- norm_edgeR(object = ps_plaque_16S, method = "TMM")
# DA analysis
da.limma <- DA_limma(
object = ps_plaque_16S,
design = ~ 1 + RSID + HMP_BODY_SUBSITE,
coef = "HMP_BODY_SUBSITESupragingival Plaque",
norm = "TMM"
)
DA <- getDA(method = da.limma, slot = "pValMat", colName = "adjP",
type = "pvalue", direction = "logFC", threshold_pvalue = 0.05,
threshold_logfc = 1, top = NULL)
# Add a priori information
DA_info <- addKnowledge(method = DA, priorKnowledge = priorInfo,
enrichmentCol = "Type", namesCol = "newNames")
# Create contingency tables and compute F tests
DA_info_enriched <- enrichmentTest(method = DA_info, enrichmentCol = "Type",
alternative = "greater")
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