follow-up about 'express' in affy / ANOVA question:wq
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@laurent-gautier-9
Last seen 10.2 years ago
Oooops... the last part of the follow-up was in french (just realized it).. As what is discussed could (still) be on general interest, I added a translation... > > * Je n'ai pas essay? le 'Cel.container mecanism' ; ce qui me para?t ?trange c'est que cel? fonctionnait avant (version 0.8) et que ?a fonctionne avec d'autres m?thodes. <translation: i="" did="" not="" try="" with="" cel.container.="" it="" looks="" strange="" since="" it="" was="" working="" in="" version="" 0.8="" and="" that="" it="" functions="" with="" other="" methods...=""> It could be caused by the nature of your data (Rafael could correct me/ add details about that... could the late addition about 'background correction' be involved ?). The Cel.container mecanism is described in the vignette ('affy.pdf'). To use it, you will have to call the step you want to use manually. In your example (note: you do not normalize. I assume you do that with good reasons): filenames <- c("path/to/file1.CEL", "path/to/file2:CEL", <and so="" on="">) lcel <- read.container.celfile(filenames=myfiles) cdf <- read.cdffile("path/to/my/cdf.file.CDF") eset <- generateExprSet(lcel, cdf, method="liwong") > Pour information, j'obtiens ?a en tapant 'traceback()': > 6: fit.li.wong(t(data.matrix), remove.outliers, normal.array.quantile, > normal.resid.quantile, large.threshold, large.variation, > outlier.fraction, delta, maxit, outer.maxit, verbose) > 5: FUN(X[[3]], ...) > 4: lapply(as.list(X), FUN, ...) > 3: sapply(data.lst, summary.stat, ...) > 2: t(sapply(data.lst, summary.stat, ...)) > 1: express(pl1, normalize = F, summary.stat = li.wong) <translation: result="" of="" the="" traceback()=""> > > * Je vais regarder genefilter, en fait je pensais que c'?tait tr?s orient? puces cDNA . Effectivement, l'id?al serait davoir une ANOVA g?ne par g?ne. <translation: i'll="" look="" at="" genefilter,="" i="" thought="" it="" was="" mainly="" meant="" for="" cdna="" arrays.="" it="" would="" be="" nice="" to="" have="" one="" anova="" per="" gene.=""> genefilter is not exactly what you want, thought learning how it work will help you to achieve your goal. The function 'filtertheniter' could also prove informative. If you do not succeed, just ask, I can come up with an 'out-of-the-box' working solution (sorry, busy today). Hopin' it helps, Laurent -------------------------------------------------------------- Laurent Gautier CBS, Building 208, DTU PhD. Student D-2800 Lyngby,Denmark tel: +45 45 25 24 85 http://www.cbs.dtu.dk/laurent
cdf genefilter cdf genefilter • 1.1k views
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