ct.prepareAnnotation | R Documentation |
This function processes a supplied annotation object for use in a pooled screening experiment.
Originally this was processed into something special, but now it essentially returns
the original annotation object in which the geneSymbol column has been factorized. This is primarily used
internally during a call to the ct.generateResults()
function. Also performs some minor functionality checking,
and ensures that the reagent identifiers are present as an 'ID' column (if absent, the row.names are used).
Valid annotations contain both 'geneID' and 'geneSymbol' columns. This is because there is often a distinction between the official gene that is being targeted and a coherent set of gRNAs that make up a testing cohort. For example, multiple sets of guides may target distinct promoters, exons, or other entities that are expected to produce distinct biological phenomena related to the gene that should be interpreted separately. For this reason, the 'geneID' column encodes the official gene designation (typically an ensembl or entrez gene identifier) while the 'geneSymbol' column contains a human-readable descriptor of the gRNA target (such as a gene symbol or promoter name). This mapping can be further expanded to incorporate mapping ambiguity via the 'ct.expandAnnotation()' function.
ct.prepareAnnotation(ann, object = NULL, controls = TRUE, throw.error = TRUE)
ann |
A |
object |
If supplied, an object with |
controls |
The name of a value in the |
throw.error |
Logical indicating whether to throw an error when |
A new annotation data frame, usually with nontargeting controls and NA values reformatted to NoTarget
(and geneID
set to 'no_gid'
), and the 'geneSymbol' column of ann
factorized. If supplied with
an object
, the gRNAs not present in the object
will be omitted.
Russell Bainer
data('ann') data('es') es <- ct.filterReads(es) newann <- ct.prepareAnnotation(ann, es)
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