Description Usage Arguments Details Value
This function creates the drseqData
slot needed by DrSeq analysis, which is
a DEXSeq::DEXSeqDataSet. This function requires two DrSeq annotation files
created by prepDrseqAnno. Two files have the same prefix (anno.prefix
),
the same suffix (anno.format
), and only differ by "exon/event".
If annotation files are missing, this function can create them freshly, which
might take some time. This function counts the RNA-seq reads on ATR events
and genes using featureCounts
.
1 2 3 4 5 6 7 8 9 10 11 12 13 | drseqCount(
event,
sampleData,
design = ~sample + exon + condition:exon,
remove.overlap.exon = FALSE,
anno.prefix = "drseq.annotation",
anno.format = "gff2",
minMQS = 10,
isPairedEnd = TRUE,
cores = max(1, detectCores() - 2),
verbose = FALSE,
...
)
|
event |
a |
sampleData |
|
design |
A formula which specifies the design of the experiment. It must specify an interaction term between a variable from the sampleData columns with the 'exon' variable. By default, the design will be '~ sample + exon + condition:exon'. This formula indicates the contrast between 'condition' and exon', i.e. differences in exon usage due to changes in the 'condition' variable. See the vignette for more examples of other designs. |
remove.overlap.exon |
|
anno.prefix |
|
anno.format |
|
minMQS, isPairedEnd |
as defined in Rsubread::featureCounts. Note that the default is customized for SURF (see details for more information). |
cores |
|
verbose |
|
... |
additional parameters for Rsubread::featureCounts. |
If you used Illumina HiSeq 2000, set strandSpecific = 2
(reversed strand).
a surf
object, with drseqData
slot updated.
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