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@lgautieralternorg-747
Last seen 9.6 years ago
> hello, > i'm trying to install BioConductor from the net. i'm following the > procedure from the web page. > when i'm on the RGui page and i type in > > source("http://www.bioconductor.org/biocLite.R")biocLite() > > i receive an error message > > Error in file(file, "r", encoding = encoding) : > unable to open connection > In addition: Warning message: > unable to connect to 'www.bioconductor.org' on port 80. > > what do i have to do? Odds are that there is a proxy between you and the website. Did you try that https://stat.ethz.ch/pipermail/bioconductor/2004-June/004984.html ? Laurent > thank you, > alessandra. > > _______________________________________________ > Bioconductor mailing list > Bioconductor at stat.math.ethz.ch > https://stat.ethz.ch/mailman/listinfo/bioconductor >
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@marie-paule-roth-1666
Last seen 9.6 years ago
Dear List, I used MBNI cdfs to have only one probe set per gene. My DE genes are now identified by custom probe set names whose structure is "database entry ID_at". These custom probeset names are different from the original Affymetrix probe IDs. Up to now, I used aafTableAnn and saveHTML to save a html table allowing easy access to very useful information such as gene symbols, descriptions, chromosome locations, genebank ids... This does not work anymore. How should I proceed to rebuild a html table, starting with the custom probe set names rather than the original Affymetrix probe set names ? Thanks for your help, Marie-Paule
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Hi Marie-Paule, Marie-Paule Roth wrote: > Dear List, > I used MBNI cdfs to have only one probe set per gene. My DE genes are now > identified by custom probe set names whose structure is "database entry > ID_at". These custom probeset names are different from the original > Affymetrix probe IDs. Up to now, I used aafTableAnn and saveHTML to save a > html table allowing easy access to very useful information such as gene > symbols, descriptions, chromosome locations, genebank ids... This does not > work anymore. How should I proceed to rebuild a html table, starting with > the custom probe set names rather than the original Affymetrix probe set > names ? I would recommend using the biomaRt package to annotate your probe sets, and htmlpage() from the annotate package to build the HTML table. Right now biomaRt and htmlpage() are not quite set up to work really well together, but Steffen Durinck and I are working to make this process much simpler. We should have something in place before the next release. In the meantime, here is a function I made to build HTML tables using biomaRt and htmlpage(). You can use this function to make lists of IDs for the 'genelist' argument of htmlpage(), and also to make lists of annotations for the 'othernames' argument. Note that this function is really inefficient unless you are using the RMySQL interface to biomaRt. In fact I wouldn't recommend using it unless you are using the RMySQL interface. ############################### ## ## Function to extract data from a mart object and return as a list ## This circumvents the problem of getBM only being able to return ## multiple queries if they all have the same length ## ## mart - a mart class object, which can be constructed using setMart() ## attributes - a vector of attributes, usually resulting ## from a call to listAttributes(mart) ## filter - The filter indicates to biomaRt where the IDs we are ## querying come from for instance, they could be an ## affy chip, Entrez Gene, UniGene, etc. ## values - The IDs that we are querying for ## ## list.names - a character vector of names for the resulting list. ## If this is used prior to a call to htmlpage(), then . ## these will be the column headings ## ############################## listBM <- function(mart, attributes, filter, values, list.names = NULL){ out <- vector("list", length(attributes)) if(is.null(list.names)) names(out) <- attributes else names(out) <- list.names if(mart at mysql){ for(j in seq(along = attributes)){ tmp <- getBM(attributes[j], filter, values, mart) tmp2 <- vector("list", length(values)) names(tmp2) <- values for(i in seq(along=tmp2)){ tst <- tmp[tmp[,1] %in% values[i],2] tst <- tst[!is.na(tst)] if(length(tst) == 0 || tst == "") tst <- " " tmp2[[i]] <- tst } out[[j]] <- tmp2 } }else{ curl <- getCurlHandle() for(j in seq(along = attributes)){ tmp2 <- vector("list", length(values)) names(tmp2) <- values for(k in seq(along = tmp2)){ tst <- getBM(attributes[j], filter, values[k], mart, curl) if(!is.null(tst)) tmp2[[k]] <- unlist(unique(tst), use.names = FALSE) else tmp2[[k]] <- " " out[[j]] <- tmp2 } } } out } HTH, Jim > Thanks for your help, > Marie-Paule > > _______________________________________________ > 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 -- James W. MacDonald, M.S. Biostatistician Affymetrix and cDNA Microarray Core University of Michigan Cancer Center 1500 E. Medical Center Drive 7410 CCGC Ann Arbor MI 48109 734-647-5623 ********************************************************** Electronic Mail is not secure, may not be read every day, and should not be used for urgent or sensitive issues.
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