Description Details Source References Examples
Similar to ProsCan_DE
, we include in this
dataset each gene's length to be passed as the second
argument to the prepare
function.
A gene's length is defined as the median length of all
its corresponding mature transcripts. In the goseq
package, length data are obtained from the UCSC genome
browser for each combination of genome
and
id
. In GOglm
, we assume that end-users
already have the length information available, so that a
column of gene lengths is properly matched to the gene
names (row names) in the data frame. For an illustration
on accessing gene length information, please see the
Example section of goglm
.
http://www.ncbi.nlm.nih.gov/pubmed/19088194
Mi G, Di Y, Emerson S, Cumbie JS and Chang JH (2012) "Length bias correction in Gene Ontology enrichment analysis using logistic regression", PLOS ONE, 7(10): e46128.
Li H, Lovci M, Kwon Y, Rosenfeld M, Fu X, et al. (2008) "Determination of tag density required for digital transcriptome analysis: application to an androgen-sensitive prostate cancer model", Proc Natl Acad Sci U S A 105: 20179-20184.
Young M, Wakefield M, Smyth G, Oshlack A (2010) "Gene ontology analysis for RNA-seq: accounting for selection bias", Genome Biol 11: R14.
Robinson M, McCarthy D, Smyth G (2010) "edgeR: a Bioconductor package for differential expression analysis of digital gene expression data", Bioinformatics 26: 139-140.
1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 | ## Load the dataset into R session:
data(ProsCan_Length)
Length_data <- ProsCan_Length
## Another dataset from this package:
data(ProsCan_DE)
DE_data <- ProsCan_DE
## Prepare a data frame to be passed to goglm():
gene_table <- prepare(DE_data, Length_data, trans.p = "d.log", trans.l = TRUE)
## Check first 10 rows of the data frame:
gene_table[1:10,1:2]
## We can call the summary() function:
summary(gene_table)
## We can also call the plot() function:
plot(gene_table)
|
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