Description Usage Arguments Value References
Note that we do not import things from goseq directly, and only load it if this function is fired. I can't figure out a way to selectively import functions from the goseq package without it having to load its dependencies, which take a long time – and I don't want loading multiGSEA to take a long time. So, the goseq package has moved to Suggests and then is loaded within this function when necessary.
1 2 3 4 5 6 7 8 9 10 11 12 13 |
gsd |
The |
selected |
The ids of the selected features |
universe |
The ids of the universe |
feature.bias |
a named vector as long as |
method |
The method to use to calculate the unbiased category enrichment scores |
repcnt |
Number of random samples to be calculated when random sampling
is used. Ignored unless |
use_genes_without_cat |
A boolean to indicate whether genes without a categorie should still be used. For example, a large number of gene may have no GO term annotated. If this option is set to FALSE, those genes will be ignored in the calculation of p-values (default behaviour). If this option is set to TRUE, then these genes will count towards the total number of genes outside the category being tested. |
do.conform |
By default |
.pipelined |
If this is being external to a multiGSEA pipeline, then
some additional cleanup of columns name output will be done. Otherwise
the column renaming and post processing is left to the do.goseq caller
(Default: |
active.only |
If |
value |
The feature_id types to extract from |
A data.table
of results, similar to goseq output. The output
from nullp
is added to the outgoing data.table as
an attribue named "pwf"
.
Young, M. D., Wakefield, M. J., Smyth, G. K., Oshlack, A. (2010). Gene ontology analysis for RNA-seq: accounting for selection bias. Genome Biology 11, R14. http://genomebiology.com/2010/11/2/R14
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