Agilent zebrafish4x44 database
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Neel Aluru ▴ 460
@neel-aluru-3760
Last seen 8.0 years ago
United States
Hello, Does any one has Agilent zebrafish 4x44 database to use for calculating % CV of replicated probes. Thank you, Neel Neel Aluru Postdoctoral Scholar Biology Department Woods Hole Oceanographic Institution Woods Hole, MA 02543 USA 508-289-3607
zebrafish zebrafish • 1.5k views
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Francois Pepin ★ 1.3k
@francois-pepin-1012
Last seen 10.3 years ago
Hi Neel. I'm not sure which database you are talking about here. I haven't used zebrafish arrays, but my experience with human and mouse is that there is very little variation between duplicated probes (ie same sequence and probe id). I would be surprised if zebrafish is any different, as those differences would be purely technical and only depend on the protocol, the reagents used and the person performing the manipulations. Maybe you could clarify if I'm not reading this properly, as I'm confused what a database would have to do with this. Francois On 11/12/2009 03:19 PM, Neel Aluru wrote: > Hello, > > Does any one has Agilent zebrafish 4x44 database to use for calculating % CV of replicated probes. > > Thank you, > > Neel > > > Neel Aluru > Postdoctoral Scholar > Biology Department > Woods Hole Oceanographic Institution > Woods Hole, MA 02543 > USA > 508-289-3607 > > _______________________________________________ > Bioconductor mailing list > Bioconductor at stat.math.ethz.ch > https://stat.ethz.ch/mailman/listinfo/bioconductor > Search the archives: http://news.gmane.org/gmane.science.biology.informatics.conductor
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Hi Francois, Thanks for your reply. I am trying to calculate the replicated probe coefficient of variation and having trouble understanding it. Here is the syntax I am writing for it. > CV.rep.probes(aa,"zebrafish.db0 ",foreground ="MeanSignal", raw.data=TRUE, writeR = TRUE, targets) The error message is Non-CTRL Replicated probes foreground: MeanSignal FILTERING BY ControlType FLAG RAW DATA: PROBES AFTER ControlType FILTERING: 42990 Error in get(mapName, envir = pkgEnv, inherits = FALSE) : object 'zebrafish.db0ACCNUM' not found Error in mget(x, envir = getAnnMap(what, chip = data, load = load), ifnotfound = NA) : error in evaluating the argument 'envir' in selecting a method for function 'mget' I defined "aa" for reading agilent FE files. I am not sure if I am doing something wrong. I really appreciate any suggestions how to proceed with it. Thanks, Sincerely, Neel On Nov 12, 2009, at 3:31 PM, Francois Pepin wrote: > Hi Neel. > > I'm not sure which database you are talking about here. > > I haven't used zebrafish arrays, but my experience with human and mouse is that there is very little variation between duplicated probes (ie same sequence and probe id). I would be surprised if zebrafish is any different, as those differences would be purely technical and only depend on the protocol, the reagents used and the person performing the manipulations. > > Maybe you could clarify if I'm not reading this properly, as I'm confused what a database would have to do with this. > > Francois > > On 11/12/2009 03:19 PM, Neel Aluru wrote: >> Hello, >> >> Does any one has Agilent zebrafish 4x44 database to use for calculating % CV of replicated probes. >> >> Thank you, >> >> Neel >> >> >> Neel Aluru >> Postdoctoral Scholar >> Biology Department >> Woods Hole Oceanographic Institution >> Woods Hole, MA 02543 >> USA >> 508-289-3607 >> >> _______________________________________________ >> Bioconductor mailing list >> Bioconductor at stat.math.ethz.ch >> https://stat.ethz.ch/mailman/listinfo/bioconductor >> Search the archives: http://news.gmane.org/gmane.science.biology.informatics.conductor > Neel Aluru Postdoctoral Scholar Biology Department Woods Hole Oceanographic Institution Woods Hole, MA 02543 USA 508-289-3607
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Hi Neel, in cases like this, supplying the sessionInfo() is a good idea, as it lets everyone know which versions you are using. As per the posting guide (see the URL at the bottom of this e-mail), having the code snippet initially would also have been helpful. I don't have the zebrafish.db0 package installed, so I can't say for sure what the issue is. I don't think you should have the space in "zebrafish.db0 ". It might also be that the zebrafish.db0 package does not have the ACCNUM mapping. Now that we've got more information, the others can chime in with more insight. Francois On 11/12/2009 09:08 PM, Neel Aluru wrote: > Hi Francois, > > Thanks for your reply. I am trying to calculate the replicated probe coefficient of variation and having trouble understanding it. Here is the syntax I am writing for it. > >> CV.rep.probes(aa,"zebrafish.db0 ",foreground ="MeanSignal", raw.data=TRUE, writeR = TRUE, targets) > The error message is > > Non-CTRL Replicated probes > foreground: MeanSignal > FILTERING BY ControlType FLAG > RAW DATA: PROBES AFTER ControlType FILTERING: 42990 > > Error in get(mapName, envir = pkgEnv, inherits = FALSE) : > object 'zebrafish.db0ACCNUM' not found > Error in mget(x, envir = getAnnMap(what, chip = data, load = load), ifnotfound = NA) : > error in evaluating the argument 'envir' in selecting a method for function 'mget' > > I defined "aa" for reading agilent FE files. > > I am not sure if I am doing something wrong. I really appreciate any suggestions how to proceed with it. > > Thanks, > > Sincerely, Neel > > On Nov 12, 2009, at 3:31 PM, Francois Pepin wrote: > >> Hi Neel. >> >> I'm not sure which database you are talking about here. >> >> I haven't used zebrafish arrays, but my experience with human and mouse is that there is very little variation between duplicated probes (ie same sequence and probe id). I would be surprised if zebrafish is any different, as those differences would be purely technical and only depend on the protocol, the reagents used and the person performing the manipulations. >> >> Maybe you could clarify if I'm not reading this properly, as I'm confused what a database would have to do with this. >> >> Francois >> >> On 11/12/2009 03:19 PM, Neel Aluru wrote: >>> Hello, >>> >>> Does any one has Agilent zebrafish 4x44 database to use for calculating % CV of replicated probes. >>> >>> Thank you, >>> >>> Neel >>> >>> >>> Neel Aluru >>> Postdoctoral Scholar >>> Biology Department >>> Woods Hole Oceanographic Institution >>> Woods Hole, MA 02543 >>> USA >>> 508-289-3607 >>> >>> _______________________________________________ >>> Bioconductor mailing list >>> Bioconductor at stat.math.ethz.ch >>> https://stat.ethz.ch/mailman/listinfo/bioconductor >>> Search the archives: http://news.gmane.org/gmane.science.biology.informatics.conductor >> > > Neel Aluru > Postdoctoral Scholar > Biology Department > Woods Hole Oceanographic Institution > Woods Hole, MA 02543 > USA > 508-289-3607 > > >
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Thanks, Francois. I am a beginner to R and slowly trying to learn. I appreciate your comments. Now I have pasted the session info. You may be right with regard to ACCNUM mapping. I looked in the zebrafish.db0 package and cannot find the ACCNUMmapping. I do not understand what you meant by space in "zebrafish.db0". Thanks once again, Sincerely, Neel Following is the session info. R version 2.9.2 (2009-08-24) Copyright (C) 2009 The R Foundation for Statistical Computing > getwd() [1] "/Users/Neel" > setwd("/Users/Neel/agilent") > getwd() [1] "/Users/Neel/agilent" Loading required package: Biobase Welcome to Bioconductor Vignettes contain introductory material. To view, type 'openVignette()'. To cite Bioconductor, see 'citation("Biobase")' and for packages 'citation(pkgname)'. Loading required package: limma Loading required package: annotate Loading required package: AnnotationDbi Loading required package: genefilter Loading required package: affyPLM Loading required package: affy Attaching package: 'affy' The following object(s) are masked from package:Agi4x44PreProcess : plotDensity Loading required package: gcrma Loading required package: Biostrings Loading required package: IRanges Attaching package: 'IRanges' The following object(s) are masked from package:base : cbind, duplicated, order, pmax, pmax.int, pmin, pmin.int, rank, rbind, rep.int, sapply, sort, table, unique Loading required package: preprocessCore Attaching package: 'affyPLM' The following object(s) are masked from package:Agi4x44PreProcess : RLE The following object(s) are masked from package:stats : resid, residuals, weights Error in loadNamespace(i[[1L]], c(lib.loc, .libPaths())) : there is no package called 'beadarray' Error: package/namespace load failed for 'arrayQualityMetrics' Loading required package: tcltk Loading Tcl/Tk interface ... done limmaGUI can be launched by typing limmaGUI() Attaching package: 'limmaGUI' The following object(s) are masked from package:limma : limmaUsersGuide limmaGUI can be launched by typing limmaGUI() Attaching package: 'limmaGUI' The following object(s) are masked from package:limma : limmaUsersGuide > library("Agi4x44PreProcess") > targets=read.targets(infile="infile.txt") Target File X FileName Treatment GErep conta cont1 conta.txt control 1 contb cont2 contb.txt control 2 contc cont3 contc.txt control 3 contd cont4 contd.txt control 4 pcba pcb1 pcba.txt pcb 1 pcbb pcb2 pcbb.txt pcb 2 pcbc pcb3 pcbc.txt pcb 3 pcbd pcb4 pcbd.txt pcb 4 > aa=read.AgilentFE(targets, makePLOT=TRUE) Read conta.txt Read contb.txt Read contc.txt Read contd.txt Read pcba.txt Read pcbb.txt Read pcbc.txt Read pcbd.txt RGList: dd$R: 'gProcessedSignal' dd$G: 'gMeanSignal' dd$Rb: 'gBGMedianSignal' dd$Gb: 'gBGUsed' > CV.rep.probes(aa, "zebrafish.db", foreground="MeanSignal", raw.data= TRUE, writeR=FALSE,targets) ------------------------------------------------------ Non-CTRL Replicated probes foreground: MeanSignal FILTERING BY ControlType FLAG RAW DATA: PROBES AFTER ControlType FILTERING: 42990 Error: getAnnMap: zebrafish.db package not attached and load is FALSE Error in mget(x, envir = getAnnMap(what, chip = data, load = load), ifnotfound = NA) : error in evaluating the argument 'envir' in selecting a method for function 'mget' > aaNORM = BGandNorm(aa, BGmethod = "half", NORMmethod = "quantile", foreground = "MeanSignal", background = "BGMedianSignal", offset = 50, makePLOTpre = TRUE, makePLOTpost = TRUE) BACKGROUND CORRECTION AND NORMALIZATION foreground: MeanSignal background: BGMedianSignal Hit <return> to see next plot: Hit <return> to see next plot: Hit <return> to see next plot: Hit <return> to see next plot: Hit <return> to see next plot: Hit <return> to see next plot: Hit <return> to see next plot: Hit <return> to see next plot: BGmethod: half NORMmethod: quantile OUTPUT in log-2 scale ------------------------------------------------------ Hit <return> to see next plot: Hit <return> to see next plot: Hit <return> to see next plot: Hit <return> to see next plot: Hit <return> to see next plot: Hit <return> to see next plot: Hit <return> to see next plot: Hit <return> to see next plot: End of the session On Nov 12, 2009, at 9:36 PM, Francois Pepin wrote: > Hi Neel, > > in cases like this, supplying the sessionInfo() is a good idea, as it lets everyone know which versions you are using. As per the posting guide (see the URL at the bottom of this e-mail), having the code snippet initially would also have been helpful. > > I don't have the zebrafish.db0 package installed, so I can't say for sure what the issue is. I don't think you should have the space in "zebrafish.db0 ". It might also be that the zebrafish.db0 package does not have the ACCNUM mapping. > > Now that we've got more information, the others can chime in with more insight. > > Francois > > On 11/12/2009 09:08 PM, Neel Aluru wrote: >> Hi Francois, >> >> Thanks for your reply. I am trying to calculate the replicated probe coefficient of variation and having trouble understanding it. Here is the syntax I am writing for it. >> >>> CV.rep.probes(aa,"zebrafish.db0 ",foreground ="MeanSignal", raw.data=TRUE, writeR = TRUE, targets) >> The error message is >> >> Non-CTRL Replicated probes >> foreground: MeanSignal >> FILTERING BY ControlType FLAG >> RAW DATA: PROBES AFTER ControlType FILTERING: 42990 >> >> Error in get(mapName, envir = pkgEnv, inherits = FALSE) : >> object 'zebrafish.db0ACCNUM' not found >> Error in mget(x, envir = getAnnMap(what, chip = data, load = load), ifnotfound = NA) : >> error in evaluating the argument 'envir' in selecting a method for function 'mget' >> >> I defined "aa" for reading agilent FE files. >> >> I am not sure if I am doing something wrong. I really appreciate any suggestions how to proceed with it. >> >> Thanks, >> >> Sincerely, Neel >> >> On Nov 12, 2009, at 3:31 PM, Francois Pepin wrote: >> >>> Hi Neel. >>> >>> I'm not sure which database you are talking about here. >>> >>> I haven't used zebrafish arrays, but my experience with human and mouse is that there is very little variation between duplicated probes (ie same sequence and probe id). I would be surprised if zebrafish is any different, as those differences would be purely technical and only depend on the protocol, the reagents used and the person performing the manipulations. >>> >>> Maybe you could clarify if I'm not reading this properly, as I'm confused what a database would have to do with this. >>> >>> Francois >>> >>> On 11/12/2009 03:19 PM, Neel Aluru wrote: >>>> Hello, >>>> >>>> Does any one has Agilent zebrafish 4x44 database to use for calculating % CV of replicated probes. >>>> >>>> Thank you, >>>> >>>> Neel >>>> >>>> >>>> Neel Aluru >>>> Postdoctoral Scholar >>>> Biology Department >>>> Woods Hole Oceanographic Institution >>>> Woods Hole, MA 02543 >>>> USA >>>> 508-289-3607 >>>> >>>> _______________________________________________ >>>> Bioconductor mailing list >>>> Bioconductor at stat.math.ethz.ch >>>> https://stat.ethz.ch/mailman/listinfo/bioconductor >>>> Search the archives: http://news.gmane.org/gmane.science.biology.informatics.conductor >>> >> >> Neel Aluru >> Postdoctoral Scholar >> Biology Department >> Woods Hole Oceanographic Institution >> Woods Hole, MA 02543 >> USA >> 508-289-3607 >> >> >> > Neel Aluru Postdoctoral Scholar Biology Department Woods Hole Oceanographic Institution Woods Hole, MA 02543 USA 508-289-3607
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Your original code had CV.rep.probes(aa,"zebrafish.db0 ",... I'm assuming this was just a typo in recopying the code, as it wouldn't work if you had the space after the 0. By sessionInfo(), I meant the output of the sessionInfo() function. What you just posted is different than before. You have an error loading beadarray and you haven't loaded zebrafish.db0, leading to a different error than originally. Please try to be consistent, otherwise it's very difficult to pinpoint the problem. As it is, I believe the issue is that Agi4x44PreProcess::CV.rep.probes always expects a ACCNUM mapping and none exist in zebrafish.db0. The solution here would be to get them to talk to one another properly. Marc, is there be a recommended way to deal with this? Is there a basic mapping that every annotation package should use? Or should a package maintainer be aware of all existing variations that exist? Francois On 11/12/2009 10:35 PM, Neel Aluru wrote: > Thanks, Francois. I am a beginner to R and slowly trying to learn. I appreciate your comments. Now I have pasted the session info. You may be right with regard to ACCNUM mapping. I looked in the zebrafish.db0 package and cannot find the ACCNUMmapping. I do not understand what you meant by space in "zebrafish.db0". > > Thanks once again, > > Sincerely, Neel > > Following is the session info. > R version 2.9.2 (2009-08-24) > Copyright (C) 2009 The R Foundation for Statistical Computing >> getwd() > [1] "/Users/Neel" >> setwd("/Users/Neel/agilent") >> getwd() > [1] "/Users/Neel/agilent" > Loading required package: Biobase > Welcome to Bioconductor > Vignettes contain introductory material. To view, type > 'openVignette()'. To cite Bioconductor, see > 'citation("Biobase")' and for packages 'citation(pkgname)'. > Loading required package: limma > Loading required package: annotate > Loading required package: AnnotationDbi > Loading required package: genefilter > Loading required package: affyPLM > Loading required package: affy > > Attaching package: 'affy' > The following object(s) are masked from package:Agi4x44PreProcess : > plotDensity > Loading required package: gcrma > Loading required package: Biostrings > Loading required package: IRanges > Attaching package: 'IRanges' > The following object(s) are masked from package:base : > > cbind, > duplicated, > order, > pmax, > pmax.int, > pmin, > pmin.int, > rank, > rbind, > rep.int, > sapply, > sort, > table, > unique > > Loading required package: preprocessCore > Attaching package: 'affyPLM' > The following object(s) are masked from package:Agi4x44PreProcess : > RLE > The following object(s) are masked from package:stats : > resid, > residuals, > weights > Error in loadNamespace(i[[1L]], c(lib.loc, .libPaths())) : > there is no package called 'beadarray' > Error: package/namespace load failed for 'arrayQualityMetrics' > Loading required package: tcltk > Loading Tcl/Tk interface ... done > > limmaGUI can be launched by typing limmaGUI() > > Attaching package: 'limmaGUI' > The following object(s) are masked from package:limma : > limmaUsersGuide > limmaGUI can be launched by typing limmaGUI() > Attaching package: 'limmaGUI' > The following object(s) are masked from package:limma : > limmaUsersGuide >> library("Agi4x44PreProcess") >> targets=read.targets(infile="infile.txt") > Target File > X FileName Treatment GErep > conta cont1 conta.txt control 1 > contb cont2 contb.txt control 2 > contc cont3 contc.txt control 3 > contd cont4 contd.txt control 4 > pcba pcb1 pcba.txt pcb 1 > pcbb pcb2 pcbb.txt pcb 2 > pcbc pcb3 pcbc.txt pcb 3 > pcbd pcb4 pcbd.txt pcb 4 > > > aa=read.AgilentFE(targets, makePLOT=TRUE) > Read conta.txt > Read contb.txt > Read contc.txt > Read contd.txt > Read pcba.txt > Read pcbb.txt > Read pcbc.txt > Read pcbd.txt > > RGList: > dd$R: 'gProcessedSignal' > dd$G: 'gMeanSignal' > dd$Rb: 'gBGMedianSignal' > dd$Gb: 'gBGUsed' > >> CV.rep.probes(aa, "zebrafish.db", foreground="MeanSignal", raw.data= TRUE, writeR=FALSE,targets) > > ------------------------------------------------------ > Non-CTRL Replicated probes > foreground: MeanSignal > FILTERING BY ControlType FLAG > RAW DATA: PROBES AFTER ControlType FILTERING: 42990 > > Error: getAnnMap: zebrafish.db package not attached and load is FALSE > Error in mget(x, envir = getAnnMap(what, chip = data, load = load), ifnotfound = NA) : > error in evaluating the argument 'envir' in selecting a method for function 'mget' > >> aaNORM = BGandNorm(aa, BGmethod = "half", NORMmethod = "quantile", foreground = "MeanSignal", background = "BGMedianSignal", offset = 50, makePLOTpre = TRUE, makePLOTpost = TRUE) > BACKGROUND CORRECTION AND NORMALIZATION > > foreground: MeanSignal > background: BGMedianSignal > Hit<return> to see next plot: > Hit<return> to see next plot: > Hit<return> to see next plot: > > Hit<return> to see next plot: > Hit<return> to see next plot: > Hit<return> to see next plot: > Hit<return> to see next plot: > Hit<return> to see next plot: > > BGmethod: half > NORMmethod: quantile > OUTPUT in log-2 scale > > ------------------------------------------------------ > Hit<return> to see next plot: > Hit<return> to see next plot: > Hit<return> to see next plot: > Hit<return> to see next plot: > Hit<return> to see next plot: > Hit<return> to see next plot: > Hit<return> to see next plot: > Hit<return> to see next plot: > End of the session > > > On Nov 12, 2009, at 9:36 PM, Francois Pepin wrote: > >> Hi Neel, >> >> in cases like this, supplying the sessionInfo() is a good idea, as it lets everyone know which versions you are using. As per the posting guide (see the URL at the bottom of this e-mail), having the code snippet initially would also have been helpful. >> >> I don't have the zebrafish.db0 package installed, so I can't say for sure what the issue is. I don't think you should have the space in "zebrafish.db0 ". It might also be that the zebrafish.db0 package does not have the ACCNUM mapping. >> >> Now that we've got more information, the others can chime in with more insight. >> >> Francois >> >> On 11/12/2009 09:08 PM, Neel Aluru wrote: >>> Hi Francois, >>> >>> Thanks for your reply. I am trying to calculate the replicated probe coefficient of variation and having trouble understanding it. Here is the syntax I am writing for it. >>> >>>> CV.rep.probes(aa,"zebrafish.db0 ",foreground ="MeanSignal", raw.data=TRUE, writeR = TRUE, targets) >>> The error message is >>> >>> Non-CTRL Replicated probes >>> foreground: MeanSignal >>> FILTERING BY ControlType FLAG >>> RAW DATA: PROBES AFTER ControlType FILTERING: 42990 >>> >>> Error in get(mapName, envir = pkgEnv, inherits = FALSE) : >>> object 'zebrafish.db0ACCNUM' not found >>> Error in mget(x, envir = getAnnMap(what, chip = data, load = load), ifnotfound = NA) : >>> error in evaluating the argument 'envir' in selecting a method for function 'mget' >>> >>> I defined "aa" for reading agilent FE files. >>> >>> I am not sure if I am doing something wrong. I really appreciate any suggestions how to proceed with it. >>> >>> Thanks, >>> >>> Sincerely, Neel >>> >>> On Nov 12, 2009, at 3:31 PM, Francois Pepin wrote: >>> >>>> Hi Neel. >>>> >>>> I'm not sure which database you are talking about here. >>>> >>>> I haven't used zebrafish arrays, but my experience with human and mouse is that there is very little variation between duplicated probes (ie same sequence and probe id). I would be surprised if zebrafish is any different, as those differences would be purely technical and only depend on the protocol, the reagents used and the person performing the manipulations. >>>> >>>> Maybe you could clarify if I'm not reading this properly, as I'm confused what a database would have to do with this. >>>> >>>> Francois >>>> >>>> On 11/12/2009 03:19 PM, Neel Aluru wrote: >>>>> Hello, >>>>> >>>>> Does any one has Agilent zebrafish 4x44 database to use for calculating % CV of replicated probes. >>>>> >>>>> Thank you, >>>>> >>>>> Neel >>>>> >>>>> >>>>> Neel Aluru >>>>> Postdoctoral Scholar >>>>> Biology Department >>>>> Woods Hole Oceanographic Institution >>>>> Woods Hole, MA 02543 >>>>> USA >>>>> 508-289-3607 >>>>> >>>>> _______________________________________________ >>>>> Bioconductor mailing list >>>>> Bioconductor at stat.math.ethz.ch >>>>> https://stat.ethz.ch/mailman/listinfo/bioconductor >>>>> Search the archives: http://news.gmane.org/gmane.science.biology.informatics.conductor >>>> >>> >>> Neel Aluru >>> Postdoctoral Scholar >>> Biology Department >>> Woods Hole Oceanographic Institution >>> Woods Hole, MA 02543 >>> USA >>> 508-289-3607 >>> >>> >>> >> > > Neel Aluru > Postdoctoral Scholar > Biology Department > Woods Hole Oceanographic Institution > Woods Hole, MA 02543 > USA > 508-289-3607 > > >
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