Converts one or more integer probe IDs back to their human-readable gene
title strings or short gene symbols using the gene annotation data frame.
This is the inverse operation of find.probe.by.gene().
Arguments
- genes
Data frame of gene annotations as returned by
extract.expression()$gene. Must contain columns"ID","Gene title", and"Gene symbol".- probe.id
Integer or character vector of one or more probe IDs to resolve, as returned by
find.probe.by.gene().- use.symbols
Logical. If
FALSE(default), returns full descriptive gene titles from the"Gene title"column, suitable for interpretation and reporting. IfTRUE, returns short gene symbols from the"Gene symbol"column, suitable for plot axis labels and any downstream tool that expects standard gene symbols such asrun.gsea().
Value
Character vector of gene names corresponding to the supplied probe
IDs. Returns empty strings "" for probes with no annotation, which
should be filtered with which(result != "").
Examples
# \donttest{
geo <- extract.expression(load.geo.soft(accession = "GDS507",
log.transform = TRUE))
#> GDS507 not found locally, downloading from NCBI GEO...
#> Using locally cached version of GDS507 found here:
#> /tmp/RtmpxRZSjV/GDS507.soft.gz
#> Using locally cached version of GPL97 found here:
#> /tmp/RtmpxRZSjV/GPL97.annot.gz
de.results <- run.limma.de(geo)
#> Removing intercept from test coefficients
top.probes <- rownames(head(de.results, 10))
# Full titles for reporting
top.titles <- get.gene.name(geo$gene, top.probes)
# Short symbols for plot labels and GSEA
top.symbols <- get.gene.name(geo$gene, top.probes, use.symbols = TRUE)
# }