Description Usage Arguments Examples
This constructs a RnaSeqParam
object, that combines
all the necessary parameters for the analysis of RNA-Seq data. As much as
possible, these parameters are determined automa-gi/ti-cally. It describes
three sets of parameters:
parameters describing the annotation
parameters describing the BAM files, i.e. the type of sequencing that was conducted.
parameters describing how the counting should be done.
The first two are provided through sepcific objects: AnnotParam
and
BamParam
respectively. The third one is a set
constituted of:
countBy: the feature per which the counts should be summarized ( exon, transcript or gene. A forth possibility - feature - can be used to define arbitrary genomic loci)
precision: the precision at which the counts should be performed:
bp or reads. bp used to be the default in the easyRNASeq
package,
whereas now reads is, following the Bioconductor main stream development.
The default parameters for the BamParam
parameter are
derived from the currently most common RNA-Seq experimental use-case:
strand-specific paired-end Illumina sequencing. See the respective manual
pages of AnnotParam
and
BamParam
for more details.
1 2 3 4 5 6 7 | ## S4 method for signature 'ANY'
RnaSeqParam(
annotParam = AnnotParam(),
bamParam = BamParam(),
countBy = c("exons", "features", "genes", "transcripts"),
precision = c("read", "bp")
)
|
annotParam |
An object derived from class |
bamParam |
An object derived from class |
countBy |
TODO |
precision |
A character value, either 'read' or 'bp' that defines the precision at which counting is done, either per read or per covered bp. 'read' is the default. |
1 2 3 4 5 6 7 8 9 10 11 12 | annotParam <- AnnotParam(
datasource=system.file(
"extdata",
"Dmel-mRNA-exon-r5.52.gff3",
package="RnaSeqTutorial"))
## create the RnaSeqParam
rsp <- RnaSeqParam(annotParam=annotParam)
## change some defaults
RnaSeqParam(countBy="features",annotParam=annotParam)
RnaSeqParam(bamParam=BamParam(stranded=TRUE,yieldSize=1L),annotParam=annotParam)
|
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