pm values
3
0
Entering edit mode
@stephen-henderson-71
Last seen 7.6 years ago
Sorry I have been looking through the vignette on Affy but am still a bit confused hot to extract the probe level data I need. I have an AffyBatch object with ca 43 (U133A) samples. Ihave 5 genes of interest that I wish to examine the probes. >Bigbatch > genes [1] "blahbla_s_at" "blahbla_s_at" "blahbla_s_at" "blahbla_s_at" [5] "blahbla_s_at" I then try >place<- pmindex(bigbatch, genes) or even >place<- pmindex(bigbatch, genes, xy=TRUE) This gives me a list of 5 sets of vectors, or 5 sets of coordinates. Now when I try >pm(bigbatch)[place[[1]]] or all sorts of variants e.g. pm(bigbatch)[,place[[1]]] I don't get the probes I am looking for at all "blahbla_s_at1 "blahbla_s_at2 etc. What do I need to be doing? Thanks Stephen ********************************************************************** This email and any files transmitted with it are confidential an... {{dropped}}
probe affy probe affy • 932 views
ADD COMMENT
0
Entering edit mode
Laurent Gautier ★ 2.3k
@laurent-gautier-29
Last seen 10.2 years ago
On Mon, Apr 14, 2003 at 03:18:58PM +0100, Stephen Henderson wrote: > Sorry I have been looking through the vignette on Affy but am still a bit > confused hot to extract the probe level data I need. > > I have an AffyBatch object with ca 43 (U133A) samples. Ihave 5 genes of > interest that I wish to examine the probes. > > >Bigbatch > > > genes > [1] "blahbla_s_at" "blahbla_s_at" "blahbla_s_at" "blahbla_s_at" > [5] "blahbla_s_at" > > I then try > >place<- pmindex(bigbatch, genes) > > or even > >place<- pmindex(bigbatch, genes, xy=TRUE) > > This gives me a list of 5 sets of vectors, or 5 sets of coordinates. > > Now when I try > > >pm(bigbatch)[place[[1]]] > or all sorts of variants e.g. > > pm(bigbatch)[,place[[1]]] > > I don't get the probes I am looking for at all "blahbla_s_at1 "blahbla_s_at2 > etc. What do I need to be doing? > > Thanks > Stephen > > Stephen, I'll assume that you are interested in the probe intensities (rather than say the probe locations on the chip). The class ProbeSet is your friend. Try: ppsets <- probeset(bigbatch, genes) par(mfrow=c(3,3)); par(ask=TRUE) barplot(ppsets[[1]]) Note: the argument 'xy=TRUE' in pmindex is deprecated. It's use is discouraged, and it should disappear sometimes. Note (bis): Few things were improved for the ProbeSet since the last release. The devel version of the pack could well be worth a look. Hopin' it helps, L. -- -------------------------------------------------------------- currently at the National Yang-Ming University in Taipei, Taiwan -------------------------------------------------------------- Laurent Gautier CBS, Building 208, DTU PhD. Student DK-2800 Lyngby,Denmark tel: +45 45 25 24 89 http://www.cbs.dtu.dk/laurent
ADD COMMENT
0
Entering edit mode
@stephen-henderson-71
Last seen 7.6 years ago
Hi Thanks for your help. Unfortunately this is not doing as I expected. Ia m on Windows, affy version 1.1.1 and > R.version.string [1] "R version 1.6.1, 2002-11-01" So > bigbatch2 AffyBatch object size of arrays=712x712 features (209917 kb) cdf=HG-U133A (22283 affyids) number of samples=53 number of genes=22283 annotation=hgu133a notes= > EWS [1] "209214_s_at" "210011_s_at" "210012_s_at" "210581_x_at" "211391_s_at" [6] "211603_s_at" "211825_s_at" > ppsets<-probeset(bigbatch2, EWS) > ppsets $"209214_s_at" ProbeSet object: id=209214_s_at pm= 11 probes $"210011_s_at" ProbeSet object: id=210011_s_at pm= 11 probes ... etc Where are the expected probe values? Do I need to change to the devel. version? -----Original Message----- From: Laurent Gautier [mailto:laurent@cbs.dtu.dk] Sent: Tuesday, April 15, 2003 12:30 AM To: Stephen Henderson Cc: bioconductor@stat.math.ethz.ch Subject: Re: [BioC] pm values On Mon, Apr 14, 2003 at 03:18:58PM +0100, Stephen Henderson wrote: > Sorry I have been looking through the vignette on Affy but am still a bit > confused hot to extract the probe level data I need. > > I have an AffyBatch object with ca 43 (U133A) samples. Ihave 5 genes of > interest that I wish to examine the probes. > > >Bigbatch > > > genes > [1] "blahbla_s_at" "blahbla_s_at" "blahbla_s_at" "blahbla_s_at" > [5] "blahbla_s_at" > > I then try > >place<- pmindex(bigbatch, genes) > > or even > >place<- pmindex(bigbatch, genes, xy=TRUE) > > This gives me a list of 5 sets of vectors, or 5 sets of coordinates. > > Now when I try > > >pm(bigbatch)[place[[1]]] > or all sorts of variants e.g. > > pm(bigbatch)[,place[[1]]] > > I don't get the probes I am looking for at all "blahbla_s_at1 "blahbla_s_at2 > etc. What do I need to be doing? > > Thanks > Stephen > > Stephen, I'll assume that you are interested in the probe intensities (rather than say the probe locations on the chip). The class ProbeSet is your friend. Try: ppsets <- probeset(bigbatch, genes) par(mfrow=c(3,3)); par(ask=TRUE) barplot(ppsets[[1]]) Note: the argument 'xy=TRUE' in pmindex is deprecated. It's use is discouraged, and it should disappear sometimes. Note (bis): Few things were improved for the ProbeSet since the last release. The devel version of the pack could well be worth a look. Hopin' it helps, L. -- -------------------------------------------------------------- currently at the National Yang-Ming University in Taipei, Taiwan -------------------------------------------------------------- Laurent Gautier CBS, Building 208, DTU PhD. Student DK-2800 Lyngby,Denmark tel: +45 45 25 24 89 http://www.cbs.dtu.dk/laurent ********************************************************************** This email and any files transmitted with it are confidential an... {{dropped}}
ADD COMMENT
0
Entering edit mode
On Wed, Apr 16, 2003 at 02:05:15PM +0100, Stephen Henderson wrote: > Hi > Thanks for your help. Unfortunately this is not doing as I expected. Ia m > on Windows, affy version 1.1.1 and However, a glance at what is below makes me believe it does what I expect. In the example, ppsets is a 'list' of elements of class 'ProbeSet' (class?ProbeSet to know more about it, like where are the probe intensities (Would something like ppsets[[i]]@pm do what you expect ?)). > > R.version.string > [1] "R version 1.6.1, 2002-11-01" > > So > > > bigbatch2 > AffyBatch object > size of arrays=712x712 features (209917 kb) > cdf=HG-U133A (22283 affyids) > number of samples=53 > number of genes=22283 > annotation=hgu133a > notes= > > > EWS > [1] "209214_s_at" "210011_s_at" "210012_s_at" "210581_x_at" "211391_s_at" > [6] "211603_s_at" "211825_s_at" > > > ppsets<-probeset(bigbatch2, EWS) > > > ppsets > $"209214_s_at" > ProbeSet object: > id=209214_s_at > pm= 11 probes > > $"210011_s_at" > ProbeSet object: > id=210011_s_at > pm= 11 probes > > ... etc > > Where are the expected probe values? Do I need to change to the devel. > version? > > -----Original Message----- > From: Laurent Gautier [mailto:laurent@cbs.dtu.dk] > Sent: Tuesday, April 15, 2003 12:30 AM > To: Stephen Henderson > Cc: bioconductor@stat.math.ethz.ch > Subject: Re: [BioC] pm values > > On Mon, Apr 14, 2003 at 03:18:58PM +0100, Stephen Henderson wrote: > > Sorry I have been looking through the vignette on Affy but am still a bit > > confused hot to extract the probe level data I need. > > > > I have an AffyBatch object with ca 43 (U133A) samples. Ihave 5 genes of > > interest that I wish to examine the probes. > > > > >Bigbatch > > > > > genes > > [1] "blahbla_s_at" "blahbla_s_at" "blahbla_s_at" "blahbla_s_at" > > [5] "blahbla_s_at" > > > > I then try > > >place<- pmindex(bigbatch, genes) > > > > or even > > >place<- pmindex(bigbatch, genes, xy=TRUE) > > > > This gives me a list of 5 sets of vectors, or 5 sets of coordinates. > > > > Now when I try > > > > >pm(bigbatch)[place[[1]]] > > or all sorts of variants e.g. > > > > pm(bigbatch)[,place[[1]]] > > > > I don't get the probes I am looking for at all "blahbla_s_at1 > "blahbla_s_at2 > > etc. What do I need to be doing? > > > > Thanks > > Stephen > > > > > > Stephen, > > I'll assume that you are interested in the probe intensities > (rather than say the probe locations on the chip). > > The class ProbeSet is your friend. > Try: > > ppsets <- probeset(bigbatch, genes) > par(mfrow=c(3,3)); par(ask=TRUE) > barplot(ppsets[[1]]) > > > Note: the argument 'xy=TRUE' in pmindex is deprecated. It's use > is discouraged, and it should disappear sometimes. > Note (bis): Few things were improved for the ProbeSet since the > last release. The devel version of the pack could well be worth > a look. > > > Hopin' it helps, > > > > > L. > -- > -------------------------------------------------------------- > currently at the National Yang-Ming University in Taipei, Taiwan > -------------------------------------------------------------- > Laurent Gautier CBS, Building 208, DTU > PhD. Student DK-2800 Lyngby,Denmark > tel: +45 45 25 24 89 http://www.cbs.dtu.dk/laurent > > > ********************************************************************** > This email and any files transmitted with it are confidential and > intended solely for the use of the individual or entity to whom they > are addressed. If you have received this email in error please notify > the system manager (wibr.mail@ucl.ac.uk). All files are scanned for viruses. > ********************************************************************** > -- -------------------------------------------------------------- currently at the National Yang-Ming University in Taipei, Taiwan -------------------------------------------------------------- Laurent Gautier CBS, Building 208, DTU PhD. Student DK-2800 Lyngby,Denmark tel: +45 45 25 24 89 http://www.cbs.dtu.dk/laurent
ADD REPLY
0
Entering edit mode
@stephen-henderson-71
Last seen 7.6 years ago
Ah thank you. that's what we need! Cheers Stephen -----Original Message----- From: Laurent Gautier [mailto:laurent@cbs.dtu.dk] Sent: Wednesday, April 16, 2003 2:26 PM To: Stephen Henderson Cc: 'Laurent Gautier'; bioconductor@stat.math.ethz.ch Subject: Re: [BioC] pm values On Wed, Apr 16, 2003 at 02:05:15PM +0100, Stephen Henderson wrote: > Hi > Thanks for your help. Unfortunately this is not doing as I expected. Ia m > on Windows, affy version 1.1.1 and However, a glance at what is below makes me believe it does what I expect. In the example, ppsets is a 'list' of elements of class 'ProbeSet' (class?ProbeSet to know more about it, like where are the probe intensities (Would something like ppsets[[i]]@pm do what you expect ?)). > > R.version.string > [1] "R version 1.6.1, 2002-11-01" > > So > > > bigbatch2 > AffyBatch object > size of arrays=712x712 features (209917 kb) > cdf=HG-U133A (22283 affyids) > number of samples=53 > number of genes=22283 > annotation=hgu133a > notes= > > > EWS > [1] "209214_s_at" "210011_s_at" "210012_s_at" "210581_x_at" "211391_s_at" > [6] "211603_s_at" "211825_s_at" > > > ppsets<-probeset(bigbatch2, EWS) > > > ppsets > $"209214_s_at" > ProbeSet object: > id=209214_s_at > pm= 11 probes > > $"210011_s_at" > ProbeSet object: > id=210011_s_at > pm= 11 probes > > ... etc > > Where are the expected probe values? Do I need to change to the devel. > version? > > -----Original Message----- > From: Laurent Gautier [mailto:laurent@cbs.dtu.dk] > Sent: Tuesday, April 15, 2003 12:30 AM > To: Stephen Henderson > Cc: bioconductor@stat.math.ethz.ch > Subject: Re: [BioC] pm values > > On Mon, Apr 14, 2003 at 03:18:58PM +0100, Stephen Henderson wrote: > > Sorry I have been looking through the vignette on Affy but am still a bit > > confused hot to extract the probe level data I need. > > > > I have an AffyBatch object with ca 43 (U133A) samples. Ihave 5 genes of > > interest that I wish to examine the probes. > > > > >Bigbatch > > > > > genes > > [1] "blahbla_s_at" "blahbla_s_at" "blahbla_s_at" "blahbla_s_at" > > [5] "blahbla_s_at" > > > > I then try > > >place<- pmindex(bigbatch, genes) > > > > or even > > >place<- pmindex(bigbatch, genes, xy=TRUE) > > > > This gives me a list of 5 sets of vectors, or 5 sets of coordinates. > > > > Now when I try > > > > >pm(bigbatch)[place[[1]]] > > or all sorts of variants e.g. > > > > pm(bigbatch)[,place[[1]]] > > > > I don't get the probes I am looking for at all "blahbla_s_at1 > "blahbla_s_at2 > > etc. What do I need to be doing? > > > > Thanks > > Stephen > > > > > > Stephen, > > I'll assume that you are interested in the probe intensities > (rather than say the probe locations on the chip). > > The class ProbeSet is your friend. > Try: > > ppsets <- probeset(bigbatch, genes) > par(mfrow=c(3,3)); par(ask=TRUE) > barplot(ppsets[[1]]) > > > Note: the argument 'xy=TRUE' in pmindex is deprecated. It's use > is discouraged, and it should disappear sometimes. > Note (bis): Few things were improved for the ProbeSet since the > last release. The devel version of the pack could well be worth > a look. > > > Hopin' it helps, > > > > > L. > -- > -------------------------------------------------------------- > currently at the National Yang-Ming University in Taipei, Taiwan > -------------------------------------------------------------- > Laurent Gautier CBS, Building 208, DTU > PhD. Student DK-2800 Lyngby,Denmark > tel: +45 45 25 24 89 http://www.cbs.dtu.dk/laurent > > > ********************************************************************** > This email and any files transmitted with it are confidential and > intended solely for the use of the individual or entity to whom they > are addressed. If you have received this email in error please notify > the system manager (wibr.mail@ucl.ac.uk). All files are scanned for viruses. > ********************************************************************** > -- -------------------------------------------------------------- currently at the National Yang-Ming University in Taipei, Taiwan -------------------------------------------------------------- Laurent Gautier CBS, Building 208, DTU PhD. Student DK-2800 Lyngby,Denmark tel: +45 45 25 24 89 http://www.cbs.dtu.dk/laurent
ADD COMMENT

Login before adding your answer.

Traffic: 878 users visited in the last hour
Help About
FAQ
Access RSS
API
Stats

Use of this site constitutes acceptance of our User Agreement and Privacy Policy.

Powered by the version 2.3.6