Thanks, Pedro. Looking forward to hearing from you.

Sincerely,
Neel

At 03:20 AM 6/18/2010, Pedro López Romero wrote:
>Thanks Neel,
>
>I am working on your data, I know where the 
>problem is.  I have to modify (or even write a 
>new function) to read the data in  such a way 
>that it is more flexible to the different data 
>formats.  I will let you know when I have this ready.
>
>p.-
>
>De: Neel Aluru [mailto:naluru@whoi.edu]
>Enviado el: Thursday, June 17, 2010 1:49 PM
>Para: Pedro López Romero; bio c bioconductor
>Asunto: RE: [BioC] AgiMicroRNA and Extra columns 
>in Agilent Mouse miRNA Microarray Release 12.0 G4471A-021828.
>
>Thanks, Pedro.
>
>Here are the details you. I have noticed that 
>what is in dd$genes and dd$other is different 
>depending on whether I use read.maimages or 
>readMicroRnaAFE function. I have pasted the details from both of them.
>
>The feature extraction software I used was version 9.3.
>
>Sincerely,
>Neel
>
>Session info () using read.maimages function
>
> > library("AgiMicroRna")
> > targets.micro=readTargets(infile="targets.txt", verbose=TRUE)
>
>Target File
>                FileName Treatment GErep Subject
>36_DMSO_1 36_DMSO_1.txt    36DMSO     1       1
>36_DMSO_2 36_DMSO_2.txt    36DMSO     1       2
>36_DMSO_3 36_DMSO_3.txt    36DMSO     1       3
>36_TCDD_1 36_TCDD_1.txt    36TCDD     2       1
>36_TCDD_2 36_TCDD_2.txt    36TCDD     2       2
>36_TCDD_3 36_TCDD_3.txt    36TCDD     2       3
>60_DMSO_1 60_DMSO_1.txt    60DMSO     3       1
>60_DMSO_2 60_DMSO_2.txt    60DMSO     3       2
>60_DMSO_3 60_DMSO_3.txt    60DMSO     3       3
>60_TCDD_1 60_TCDD_1.txt    60TCDD     4       1
>60_TCDD_2 60_TCDD_2.txt    60TCDD     4       2
>60_TCDD_3 60_TCDD_3.txt    60TCDD     4       3
>
> > ddaux=read.maimages(files=targets.micro$FileName,source="agilent",
>+ other.columns=list(IsGeneDetected="gIsGeneDetected",
>+ IsSaturated="gIsSaturated",
>+ IsFeatNonUnifOF="gIsFeatNonUnifOL",
>+ IsFeatPopnOL="gIsFeatPopnOL",
>+ ChrCoord="chr_coord", BGKmd="gBGMedianSignal",
>+ BGKus="gBGUsed"),
>+ columns=list(Rf="gTotalGeneSignal",
>+ Gf="gTotalProbeSignal",
>+ Rb="gMeanSignal",Gb="gProcessedSignal"), verbose=TRUE,sep="\t",quote="")
>Read 36_DMSO_1.txt
>Read 36_DMSO_2.txt
>Read 36_DMSO_3.txt
>Read 36_TCDD_1.txt
>Read 36_TCDD_2.txt
>Read 36_TCDD_3.txt
>Read 60_DMSO_1.txt
>Read 60_DMSO_2.txt
>Read 60_DMSO_3.txt
>Read 60_TCDD_1.txt
>Read 60_TCDD_2.txt
>Read 60_TCDD_3.txt
> > names(ddaux)
>[1] "R"       "G"       "Rb"      "Gb"      "targets" "genes"   "source"
>[8] "other"
> > names(ddaux$genes)
>  [1] "Row"            "Col"            "Start"          "Sequence"
>  [5] "ProbeUID"       "ControlType"    "ProbeName"      "GeneName"
>  [9] "SystematicName" "Description"
> > names(ddaux$other)
>[1] 
>"gIsGeneDetected"  "gIsSaturated"     "gIsFeatNonUnifOL" "gIsFeatPopnOL"
>[5] "gBGMedianSignal"  "gBGUsed"
>
>Session Info () with AgiMicroRnaAFE function.
>
> > ddaux=readAgiMicroRnaAFE(targets.micro, verbose=TRUE)
>Error: could not find function "readAgiMicroRnaAFE"
> > ddaux=readMicroRnaAFE(targets.micro, verbose=TRUE)
>Read 36_DMSO_1.txt
>Read 36_DMSO_2.txt
>Read 36_DMSO_3.txt
>Read 36_TCDD_1.txt
>Read 36_TCDD_2.txt
>Read 36_TCDD_3.txt
>Read 60_DMSO_1.txt
>Read 60_DMSO_2.txt
>Read 60_DMSO_3.txt
>Read 60_TCDD_1.txt
>Read 60_TCDD_2.txt
>Read 60_TCDD_3.txt
>
>   RGList:
>         dd$R:           'gTotalGeneSignal'
>         dd$G:           'gTotalProbeSignal'
>         dd$Rb:          'gMeanSignal'
>         dd$Gb:          'gProcessedSignal'
>
> > names(ddaux)
>[1] "R"       "G"       "Rb"      "Gb"      "targets" "genes"   "other"
> > names(ddaux$genes)
>[1] "Sequence"    "ProbeUID"    "ControlType"
> > names(ddaux$other)
>[1] 
>"gIsGeneDetected"  "gIsSaturated"     "gIsFeatNonUnifOL" "gIsFeatPopnOL"
>[5] "gBGMedianSignal"  "gBGUsed"
>
>
>
>At 04:29 AM 6/17/2010, Pedro López Romero wrote:
>
>Hi Neel,
>
>I think your problem with the filtering 
>function, is not the filtering itself but when 
>the function tries to write an output. I am 
>modifying this, so the user can choose whether 
>or not they want to have an output file in the 
>filtering step. In the meantime, can you tell me what you have in?
>names(dd),
>names(dd$genes)
>names(dd$genes)
>names(dd$other)
>
>What version of the Extractor are you using?
>
>
>
>p.-
>
>De: Neel Aluru [ mailto:naluru@whoi.edu]
>Enviado el: Wednesday, June 16, 2010 10:54 PM
>Para: Richard Friedman; Pedro López Romero; bio c bioconductor
>Asunto: Re: [BioC] AgiMicroRNA and Extra columns 
>in Agilent Mouse miRNA Microarray Release 12.0 G4471A-021828.
>
>Hi Rich,
>
>Did you try filtering probes using 
>FilterMicroRna function after removing the two 
>columns. I am having difficulty in filtering probes.
>
>Thanks,
>Neel
>
>At 04:19 PM 6/16/2010, Richard Friedman wrote:
>
>Dear Pedro and List,
>
>         My text files form Agilent  Mouse miRNA Microarray Release 12.0
>G4471A-021828 has two extra columns which are not
>in  GSE19232  Agilent human microRNA array v 2.0 (G44708) - "start"
>and "sequence". When these are deleted
>AgiMicroRNA  works. I do not know if this is due to the array or
>software or processing options on the software.
>This clears up the problem with maMicroRna( which i have been writing
>you about. It would be nice if
>this could be taken into  automatically in a future version of
>AgiMicroRNA, but this solves my porblem for now.
>
>Thanks and best wishes,
>Rich
>------------------------------------------------------------
>Richard A. Friedman, PhD
>Associate Research Scientist,
>Biomedical Informatics Shared Resource
>Herbert Irving Comprehensive Cancer Center (HICCC)
>Lecturer,
>Department of Biomedical Informatics (DBMI)
>Educational Coordinator,
>Center for Computational Biology and Bioinformatics (C2B2)/
>National Center for Multiscale Analysis of Genomic Networks (MAGNet)
>Room 824
>Irving Cancer Research Center
>Columbia University
>1130 St. Nicholas Ave
>New York, NY 10032
>(212)851-4765 (voice)
>friedman@cancercenter.columbia.edu
><http://cancercenter.columbia.edu/~friedman/>http://cancercenter.columbia.edu/~friedman/
>
>In Memoriam,
>George Scithers
>
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>
>Neel Aluru Ph.D.
>Post doctoral Scholar
>Biology Department
>Redfield 304 (MS#32)
>Woods Hole Oceanographic Institution
>Woods Hole MA 02543 USA
>Phone: (508) 289-3607 [Office]
>774-392-3727 [Cell]
>RID: A-7237-2009
>
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>Woods Hole Oceanographic Institution
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>Este mensaje va dirigido, de manera exclusiva, a 
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>En caso de haber recibido este mensaje por 
>error, le rogamos que, de forma inmediata, nos 
>lo comunique mediante correo electrónico 
>remitido a nuestra atención o a través del 
>teléfono (+34 914531200) y proceda a su 
>eliminación, así como a la de cualquier 
>documento adjunto al mismo. Asimismo, le 
>comunicamos que la distribución, copia o 
>utilización de este mensaje, o de cualquier 
>documento adjunto al mismo, cualquiera que fuera 
>su finalidad, están prohibidas por la ley. Le 
>informamos, como destinatario de este mensaje, 
>que el correo electrónico y las comunicaciones 
>por medio de Internet no permiten asegurar ni 
>garantizar la confidencialidad de los mensajes 
>transmitidos, así como tampoco su integridad o 
>su correcta recepción, por lo que el CNIC no 
>asume responsabilidad alguna por tales 
>circunstancias. Si no consintiese la utilización 
>del correo electrónico o de las comunicaciones 
>vía Internet le rogamos nos lo comunique y ponga 
>en nuestro conocimiento de manera inmediata.
>
>
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>This message is intended exclusively for the 
>person to whom it is addressed and contains 
>privileged and confidential information 
>protected from disclosure by law. If you are not 
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Neel Aluru Ph.D.
Post doctoral Scholar
Biology Department
Redfield 304 (MS#32)
Woods Hole Oceanographic Institution
Woods Hole MA 02543 USA
Phone: (508) 289-3607 [Office]
774-392-3727 [Cell]
RID: A-7237-2009  
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