qtex,ERVmapParam-method | R Documentation |
The qtex()
method quantifies transposable element expression.
## S4 method for signature 'ERVmapParam'
qtex(
x,
phenodata = NULL,
mode = ovUnion,
yieldSize = 1000000L,
verbose = 1,
BPPARAM = SerialParam(progressbar = ifelse(verbose == 1, TRUE, FALSE))
)
## S4 method for signature 'TEtranscriptsParam'
qtex(
x,
phenodata = NULL,
mode = ovUnion,
yieldSize = 1000000L,
BPPARAM = SerialParam(progressbar = TRUE)
)
## S4 method for signature 'TelescopeParam'
qtex(
x,
phenodata = NULL,
mode = ovUnion,
yieldSize = 1000000L,
auxiliaryFeatures = FALSE,
BPPARAM = SerialParam(progressbar = TRUE)
)
## S4 method for signature 'atenaParam'
qtex(
x,
phenodata = NULL,
mode = ovUnion,
yieldSize = 1000000L,
auxiliaryFeatures = FALSE,
BPPARAM = SerialParam(progressbar = TRUE)
)
x |
An
|
phenodata |
A |
mode |
One of the pre-defined overlapping methods such as
|
yieldSize |
Field inherited from |
verbose |
(Default 1). When |
BPPARAM |
An object of a BiocParallelParam subclass
to configure the parallel execution of the code. By default,
a SerialParam object is used, which does not use
any parallelization, with the flag |
auxiliaryFeatures |
(Default |
Giving some AtenaParam
object sub-class as input, the
qtex()
method quantifies the expression of transposable
elements (TEs). The particular algorithm to perform the
quantification will be selected depending on the specific
sub-class of input AtenaParam
object, see argument
x
above.
A SummarizedExperiment object.
Jin Y et al. TEtranscripts: a package for including transposable elements in differential expression analysis of RNA-seq datasets. Bioinformatics. 2015;31(22):3593-3599. DOI: https://doi.org/10.1093/bioinformatics/btv422
Tokuyama M et al. ERVmap analysis reveals genome-wide transcription of human endogenous retroviruses. PNAS, 115(50):12565-12572, 2018. https://doi.org/10.1073/pnas.1814589115
Bendall ML et al. Telescope: characterization of the retrotranscriptome by accurate estimation of transposable element expression. PLOS Computational Biology, 15:e1006453, 2019. https://doi.org/10.1371/journal.pcbi.1006453
TEtranscriptsParam
ERVmapParam
TelescopeParam
bamfiles <- list.files(system.file("extdata", package="atena"),
pattern="*.bam", full.names=TRUE)
## Not run:
## use the following two instructions to fetch annotations, they are here
## commented out to enable running this example quickly when building and
## checking the package
rmskat <- annotaTEs(genome="dm6", parsefun=rmskatenaparser,
strict=FALSE, insert=500)
rmskLTR <- getLTRs(rmskat, relLength=0.8,
fullLength=TRUE,
partial=TRUE,
otherLTR=TRUE)
## End(Not run)
## DO NOT TYPE THIS INSTRUCTION, WHICH JUST LOADS A PRE-COMPUTED ANNOTATION
## YOU SHOULD USE THE INSTRUCTIONS ABOVE TO FETCH ANNOTATIONS
rmskLTR <- readRDS(system.file("extdata", "rmskatLTRrlen80flenpartoth.rds",
package="atena"))
## build a parameter object for Telescope
tspar <- TelescopeParam(bfl=bamfiles,
teFeatures=rmskLTR,
singleEnd=TRUE,
ignoreStrand=TRUE)
## quantify expression
qts <- qtex(tspar)
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