Description Usage Arguments Details Value Author(s) Examples
View source: R/Modifier-Inosine-class.R
Inosine can be detected in RNA-Seq data by the conversion of A positions to
G. This conversion is detected by ModInosine
and used to search for
Inosine positions. dataType
is "PileupSequenceData"
.
Only samples labeled with the condition treated
are used for this
analysis, since the A to G conversion is common feature among the reverse
transcriptases usually emploied. Let us know, if that is not the case, and
the class needs to be modified.
Further information on Functions
of
ModInosine
.
1 2 3 | ModInosine(x, annotation, sequences, seqinfo, ...)
ModSetInosine(x, annotation = NA, sequences = NA, seqinfo = NA, ...)
|
x |
the input which can be of the different types depending on whether
a |
annotation |
annotation data, which must match the information contained
in the BAM files. This is parameter is only required, if |
sequences |
sequences matching the target sequences the reads were
mapped onto. This must match the information contained in the BAM files. This
is parameter is only required, if |
seqinfo |
An optional |
... |
Optional arguments overwriting default values, which are
|
ModInosine
score: the scores for reported Inosine positions are
between 0 and 1. They are calculated as the relative amount of called G bases
((G / N)
) and only saved for genomic A positions.
a ModInosine
or ModSetInosine
object
Felix G.M. Ernst [aut]
1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 | # construction of ModInosine object
library(RNAmodR.Data)
library(rtracklayer)
annotation <- GFF3File(RNAmodR.Data.example.man.gff3())
sequences <- RNAmodR.Data.example.man.fasta()
files <- c(treated = RNAmodR.Data.example.wt.1())
mi <- ModInosine(files,annotation = annotation ,sequences = sequences)
# construction of ModSetInosine object
## Not run:
files <- list("SampleSet1" = c(treated = RNAmodR.Data.example.wt.1(),
treated = RNAmodR.Data.example.wt.2(),
treated = RNAmodR.Data.example.wt.3()),
"SampleSet2" = c(treated = RNAmodR.Data.example.bud23.1(),
treated = RNAmodR.Data.example.bud23.2()),
"SampleSet3" = c(treated = RNAmodR.Data.example.trm8.1(),
treated = RNAmodR.Data.example.trm8.2()))
msi <- ModSetInosine(files, annotation = annotation, sequences = sequences)
## End(Not run)
|
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