NOTE: This method applies only to Affymetrix tiling arrays! Furthermore, it is likely to be more useful for promoter tiling arrays and less so for whole-genome tiling arrays.
"bpmapCluster2Cdf"(pathname, chipType, tags=NULL, rows, cols, maxProbeDistance=3000L, minNbrOfProbes=30L, groupName=gsub("_.*", "", chipType), field="fullname", stringRemove=sprintf("%s:.*;", groupName), ..., flavor=c("v2", "v1"), path="*", verbose=-10)
integer
s specifying the probe dimension
of the chip. It is important to get this correct. They can be
inferred from the CEL header of a CEL file for this chip,
cf. readCelHeader
.integer
specifying the maximum
genomic distance (in basepairs) allowed between two probes in order
to "cluster" those two probes into the same CDF units. Whenever the
distance is greater, the two probes end up in two different CDF units.integer
specifying the minimum number
of probes required in a CDF unit. If fewer, those probes are dropped.character
string specifying which BPMAP sequences
to keep. Sequence with this group name is kept, all others are
excluded.character
string.readBpmap
."*"
(default), it will be written to
annotationData/chipTypes//
.Verbose
."v2"
replaced "v1"
as aroma.affymetrix v2.5.4
(June 21, 2012). For details, see news(package="aroma.affymetrix")
.