Entering edit mode
Ariel Grostern
▴
80
@ariel-grostern-4705
Last seen 10.3 years ago
Hi,
I am attempting to adapt the makeProbePackage function in
AnnotationDbi to
permit me to make a probe package for my PM-only Affy array, so that I
can
then use altcdfenvs to re-annotate the probes. My probe sequence file
is set
up exactly as the normal tab-limited PM/MM file.
>From examining the makeProbePackage.R file, it appears that there is
only
limited referral to MM probes, so I am eliminating them (see below).
However, there is one section that I don't know what to do with:
## On most chips, PM and MM probe are next to each other on the chip,
at
same
## x coordinate and at adjacent y coordinates. Then, "sizex" is
always the
same,
## namely the size of the chip in x-direction. On some chips, there
are
few
## exceptions.
tab = table(mm1-pm1)
## WHAT TO DO FOR THE ABOVE LINE?
sizex = as.numeric(names(tab))[ max(tab)==tab ]
can I replace the "tab" line with:
tab=table(pm1)
Thanks for any input,
Ariel
##
----------------------------------------------------------------------
## The table pt contains a probe to probe-set mapping (many-to-one).
## The CDF environment contains a probe-set to probe mapping (one-to-
many).
## Here, we check whether they agree.
## In addition, it uses the information in the CDF to guess
## sizex, the size of the chip in x-direction.
## This is done using the fact that with current-day Affymetrix
## for each PM probe at (x,y) there is a MM probe at (x,y+1).
## (C) Laurent Gautier, Wolfgang Huber 2003
##
----------------------------------------------------------------------
.lgExtraParanoia = function (pt, cdfname) {
do.call(library, list(cdfname))
thecdf <- as.environment(paste("package", cdfname,
sep=":"))[[cdfname]]
## Unroll CDF in order to invert the mapping from probe-set -> probe
## to probe -> probe-set. psnm1[i] is the probe set name for the
i-th
probe
probesetnames = ls(thecdf)
pm1 = unlist(lapply(probesetnames,
function(ps) {thecdf[[ps]][,1]}))
## Crossed out the mm1 function
##mm1 = unlist(lapply(probesetnames,
## function(ps) {thecdf[[ps]][,2]}))
psnm1 = unlist(lapply(probesetnames,
function(ps) {rep(ps, nrow(thecdf[[ps]]))}))
## On most chips, PM and MM probe are next to each other on the
chip, at
same
## x coordinate and at adjacent y coordinates. Then, "sizex" is
always the
same,
## namely the size of the chip in x-direction. On some chips, there
are
few
## exceptions.
##tab = table(mm1-pm1)
tab = table(pm1)
## WHAT TO DO FOR THE ABOVE LINE?
sizex = as.numeric(names(tab))[ max(tab)==tab ]
## The probe indices according to pt
pm2 = pt$y * sizex + pt$x + 1
## Crossed out the mm2 function
## mm2 = (pt$y+1) * sizex + pt$x + 1
psnm2 = pt[["Probe.Set.Name"]]
## Check if the probe set names that are associated with each probe
## are the same in both CDF and pt
## z1 = z2 = rep(NA, max(pm1, mm1, pm2, mm2))
## z1[pm1] = z1[mm1] = psnm1
## z2[pm2] = z2[mm2] = psnm2
## Remove mm1 and mm3 referals
z1 = z2 = rep(NA, max(pm1, pm2))
z1[pm1] = psnm1
z2[pm2] = psnm2