[BioC] how to use limma on this format
smohapat at vbi.vt.edu
smohapat at vbi.vt.edu
Tue Jul 17 14:09:52 CEST 2007
Hello Weiwei:
Limma function read.maimages reads agilent data files.
> ?read.maimages
---------
Description
Reads an RGList from a series of two-color microarray image analysis
output files
...
Arguments
source: character string specifying the image analysis program which
produced the output files. Choices are "generic", "agilent",
"arrayvision", "bluefuse", "genepix", "genepix.custom", "genepix.median",
"imagene", "quantarray", "scanarrayexpress", "smd.old", "smd", "spot" or
"spot.close.open".
...
---------
By default it reads the following columns for agilent.
G = "gMeanSignal",
Gb = "gBGMedianSignal",
R = "rMeanSignal",
Rb = "rBGMedianSignal")
Best wishes,
Saroj
On Mon, July 16, 2007 7:45 pm, Weiwei Shi wrote:
> Hi, there:
>
>
> I have an agilent data format with colnames which look like the
> followings. I am wondering how to proceed with this data by using limma to
> do the QC. I mean, I probably can create some corresponding objects of
> limma manually (like RGList from gMedianSignal...) but it is painful.
> Anyone knows about this source or any suggestions to move
> from there.
>
> Another question, can I find "locuslink id" for ProbeName for agilent?
>
>
> thanks,
>
> the data columns are
>> as.character(t0[9,])
> [1] "FEATURES" "FeatureNum"
> "Row"
> [4] "Col" "Start"
> "Sequence"
> [7] "ProbeUID" "ControlType"
> "ProbeName"
> [10] "GeneName" "PositionX"
> "PositionY"
> [13] "LogRatio" "LogRatioError"
> "PValueLogRatio"
> [16] "gSurrogateUsed" "rSurrogateUsed"
> "gIsFound"
> [19] "rIsFound" "gProcessedSignal"
> "rProcessedSignal"
> [22] "gProcessedSigError" "rProcessedSigError"
> "gNumPixOLHi"
> [25] "rNumPixOLHi" "gNumPixOLLo"
> "rNumPixOLLo"
> [28] "gNumPix" "rNumPix"
> "gMeanSignal"
> [31] "rMeanSignal" "gMedianSignal"
> "rMedianSignal"
> [34] "gPixSDev" "rPixSDev"
> "gBGNumPix"
> [37] "rBGNumPix" "gBGMeanSignal"
> "rBGMeanSignal"
> [40] "gBGMedianSignal" "rBGMedianSignal"
> "gBGPixSDev"
> [43] "rBGPixSDev" "gNumSatPix"
> "rNumSatPix"
> [46] "gIsSaturated" "rIsSaturated"
> "PixCorrelation"
> [49] "BGPixCorrelation" "gIsFeatNonUnifOL"
> "rIsFeatNonUnifOL"
> [52] "gIsBGNonUnifOL" "rIsBGNonUnifOL"
> "gIsFeatPopnOL"
> [55] "rIsFeatPopnOL" "gIsBGPopnOL"
> "rIsBGPopnOL"
> [58] "IsManualFlag" "gBGSubSignal"
> "rBGSubSignal"
> [61] "gBGSubSigError" "rBGSubSigError"
> "BGSubSigCorrelation"
> [64] "gIsPosAndSignif" "rIsPosAndSignif"
> "gPValFeatEqBG"
> [67] "rPValFeatEqBG" "gNumBGUsed"
> "rNumBGUsed"
> [70] "gIsWellAboveBG" "rIsWellAboveBG"
> "gBGUsed"
> [73] "rBGUsed" "gBGSDUsed"
> "rBGSDUsed"
> [76] "IsNormalization" "gDyeNormSignal"
> "rDyeNormSignal"
> [79] "gDyeNormError" "rDyeNormError"
> "DyeNormCorrelation"
> [82] "ErrorModel" "xDev"
> "gSpatialDetrendIsInFilteredSet"
> [85] "rSpatialDetrendIsInFilteredSet" "gSpatialDetrendSurfaceValue"
> "rSpatialDetrendSurfaceValue"
> [88] "" ""
> ""
>
>
>
>
> --
> Weiwei Shi, Ph.D
> Research Scientist
> GeneGO, Inc.
>
>
> "Did you always know?"
> "No, I did not. But I believed..."
> ---Matrix III
>
>
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