altcdfenvs/DESCRIPTION0000644000175200017520000000216514710267405015445 0ustar00biocbuildbiocbuildPackage: altcdfenvs Version: 2.68.0 Title: alternative CDF environments (aka probeset mappings) Author: Laurent Gautier Maintainer: Laurent Gautier biocViews: Microarray, OneChannel, QualityControl, Preprocessing, Annotation, ProprietaryPlatforms, Transcription Depends: R (>= 2.7), methods, BiocGenerics (>= 0.1.0), S4Vectors (>= 0.9.25), Biobase (>= 2.15.1), affy, makecdfenv, Biostrings, hypergraph Suggests: plasmodiumanophelescdf, hgu95acdf, hgu133aprobe, hgu133a.db, hgu133acdf, Rgraphviz, RColorBrewer Description: Convenience data structures and functions to handle cdfenvs License: GPL (>= 2) Collate: appendCdfEnvAffy.R buildCdfEnv.matchprobes.R buildCdfEnv.biostrings.R CdfEnv.R cdfenvs.R copyCdfEnvAffy.R readFASTA.R removeIndex.R unique.CdfEnvAffy.R LazyLoad: yes Packaged: 2024-10-29 23:25:57 UTC; biocbuild git_url: https://git.bioconductor.org/packages/altcdfenvs git_branch: RELEASE_3_20 git_last_commit: 53038c8 git_last_commit_date: 2024-10-29 Repository: Bioconductor 3.20 Date/Publication: 2024-10-29 NeedsCompilation: no altcdfenvs/MD50000644000175200017520000000541014710267405014243 0ustar00biocbuildbiocbuild24d9103cded99965787b9ee2adddbaf5 *DESCRIPTION f8aae127dcc6fdaf96a604f359833f7f *NAMESPACE 2d4f779d7dd27935e94781da7335eb6a *R/CdfEnv.R 630c972d179828bb31b8cf776de09370 *R/appendCdfEnvAffy.R 3c213a33242d27a0a3e54ea978b456aa *R/buildCdfEnv.biostrings.R 2167977873ec87a8e95f5b576f2f047f *R/buildCdfEnv.matchprobes.R 25115096c4bf3d005f929145a6700cdb *R/cdfenvs.R c202d3ca1af6dada77849e0ca37610c5 *R/copyCdfEnvAffy.R 5bcc736d810b95dacc026ada63a89d2b *R/readFASTA.R a39d8fd6ea7b43a57c072d6c429e381a *R/removeIndex.R 014e6d45240b9219f0dc9bbe300f17bc *R/unique.CdfEnvAffy.R 937ae3c808d8383fdf8eab4302925dd4 *build/vignette.rds fb787de9457f21aeccc82923652aafc0 *data/cdfenvEx.rda ebf92d5b4e68128d31a3e9249f0fa6b1 *inst/CITATION 0a53f074a258da10446d67b6f097aacc *inst/UnitTests/AffyProbesMatch_test.R 23c88219b41cca5c18a3118ad76fd253 *inst/doc/altcdfenvs.R acf8b6c53ba422df216c4c956dda3513 *inst/doc/altcdfenvs.Rnw 7a934f26bb7839bb05cd57bb3f7f6dc1 *inst/doc/altcdfenvs.pdf 56059c9e040af1482ae4e66289cbfad7 *inst/doc/modify.R 48f6ceae6f5d07787409d0958942cba2 *inst/doc/modify.Rnw d49efc032533005221ddec8f48b9e45d *inst/doc/modify.pdf 1423e166149e40b99c91194a3e68bd91 *inst/doc/ngenomeschips.R a8ef75c14c4bc3c5ee565629183f245b *inst/doc/ngenomeschips.Rnw 7616c785d98d7a75127999f4f773cb21 *inst/doc/ngenomeschips.pdf 7499a24844858824a246ca8ef35be87d *inst/exampleData/Plasmodium-Probeset-IDs.txt 9e2e95d99c194250d94f4cc0b6f40fd4 *inst/exampleData/sample.fasta b4571cde85de0a3298b4fecb3110406c *inst/exampleData/slamf_targets.RData 8760e3eaecf5a33901680efd0d24b781 *inst/internalData/chipspecs.tab 24e7ee02b48c4070fda2e8d3be1ea151 *man/AffyProbesMatch-class.Rd 190c943b0f75e444a48757cefcfc120c *man/CdfEnvAffy-class.Rd 35677a60633398d5271f0617fc6c14cf *man/appendCdfEnvAffy.Rd 7b9097d5d4b4b6df24ee9c0358c33d4a *man/buildCdfEnv.biostrings.Rd 951643a1848aed198beddec759e83307 *man/cdfenv.Rd 835beb07c1664dd1377239bb4fd942f2 *man/cdfenvEx.Rd 18654d4f2846298a12225b57cc7edb7a *man/copyCdfEnvAffy.Rd 2727564377fa68de567dcdb6708cfb97 *man/countduplicated.Rd aed306c6c7497d3e8f44f40c3748e799 *man/geneNames.Rd 6ba0156252507dfe5aa806ae4d13e2ad *man/getxy.probeseq.Rd 21d8d5f4cefe4aee08063c8351ccd012 *man/index2xy.Rd 079cd1542f83b26d5a980df05e96433a *man/indexProbes.CdfEnvAffy.Rd a759a58a25669ad65c90bdda002d6cdc *man/matchAffyProbes.Rd 93ffd8f221fa4afe61fe799330ac7736 *man/plot.CdfEnvAffy.Rd 6ac4ff5830aef991c38262a7c6458d0f *man/removeIndex.Rd f6b600cba47a7c70bae67bc8ffdc8f0c *man/toHypergraph.Rd fc3d1cd6c84aa2eb546344dc792eb9e6 *man/unique.CdfEnvAffy.Rd cb5535dbe904e8b45df3efcbf0ea03f8 *man/utils.FASTA.Rd 7892cdd47dd7d01c02b953a6f57059a8 *man/validAffyBatch.Rd acf8b6c53ba422df216c4c956dda3513 *vignettes/altcdfenvs.Rnw 48f6ceae6f5d07787409d0958942cba2 *vignettes/modify.Rnw a8ef75c14c4bc3c5ee565629183f245b *vignettes/ngenomeschips.Rnw altcdfenvs/NAMESPACE0000644000175200017520000000022114710217111015132 0ustar00biocbuildbiocbuild importFrom(graphics, plot) importFrom("BiocGenerics", "combine") import(S4Vectors) importFrom("affy", "indexProbes") exportPattern("^[^\\.]") altcdfenvs/R/0000755000175200017520000000000014710217111014121 5ustar00biocbuildbiocbuildaltcdfenvs/R/CdfEnv.R0000644000175200017520000001632014710217111015413 0ustar00biocbuildbiocbuild index2xy.CdfEnvAffy <- function(object, i) { indices2xy(i, nc = object@nrow) - getOption("BioC")$affy$xy.offset } xy2index.CdfEnvAffy <- function(object, x, y) { o <- getOption("BioC")$affy$xy.offset xy2indices(x+o, y+o, nc = object@nrow) } setClass("CdfEnvAffy", representation(envir = "environment", envName = "character", index2xy = "function", xy2index = "function", nrow = "integer", ncol = "integer", probeTypes = "character", chipType = "character"), prototype = list(index2xy = index2xy.CdfEnvAffy, xy2index = xy2index.CdfEnvAffy)) ## --- setAs("CdfEnvAffy", "environment", function(from) from@envir ) setAs("CdfEnvAffy", "Cdf", function(from) { m <- matrix(as.numeric(NA), from@nrow, from@ncol) l <- ls(from@envir) for (i in seq(along=l)) { tmp <- indexProbes(from, "pm", l[i])[[1]] m[tmp] <- i tmp <- indexProbes(from, "mm", l[i])[[1]] m[tmp] <- i } cdf <- new("Cdf", cdfName=from@chipType, name=m, name.levels=l) return(cdf) } ) geneNames.CdfEnvAffy <- function(object) { ls(as(object, "environment")) } setMethod("geneNames", "CdfEnvAffy", geneNames.CdfEnvAffy) ## --- setMethod("[", signature(x="CdfEnvAffy", i="character", j="missing", drop="missing"), function(x, i, j, drop=FALSE) { if( !missing(j)) { stop("Improper subsetting. Only one vector of IDs should be given.\n") } if (is.matrix(i)) { if (! is.integer(i)) { stop("not implemented") ##stop("when a matrix, 'i' should be of mode 'integer'") } y <- x y@envName <- paste(x@envName, "-subsetXYcoords", sep="") y@envir <- new.env(hash=TRUE, parent = emptyenv()) ## make a Cdf (faster lookup for XY or indexes). cdfenv <- get(x@envName) cdf <- as(cdfenv, "Cdf") idx <- xy2index(x, i) for (i in idx) { id <- cdf@names.level[cdf@names[i]] tmp <- indexProbes(y, y@probeTypes, id) ## implementation not complete ## pm or mm to be sorted ## and idx appended to tmp assign(id, tmp, envir=y@envir) } } else { if (! is.character(i)) { stop("when not a matrix, 'i' should be of mode 'character'") } y <- x y@envName <- paste(x@envName, "-subsetProbeSets", sep="") y@envir <- new.env(hash=TRUE, parent = emptyenv()) for (id in i) { ##tmp <- indexProbes(x, x@probeTypes, id) tmp <- do.call(cbind, lapply(x@probeTypes, function(pt) indexProbes(x, pt, id)[[1]])) assign(id, tmp, envir=y@envir) } } return(y) }) ## --- indexProbes.CdfEnvAffy <- function(object, which, probeSetNames=NULL) { probeTypes <- object@probeTypes ##FIXME: hack for compatibility with 'affy' if (identical(which, "both") || identical(which, c("pm", "mm", "both"))) { which <- probeTypes warning("The use of \"both\" in 'which' is deprecated.") } ## if ( ! all(which %in% probeTypes)) stop(paste("'which' can only take values from:", paste(probeTypes, collapse=", "))) i.probes <- match(which, probeTypes) envir <- as(object, "environment") if(is.null(probeSetNames)) probeSetNames <- ls(envir) ans <- mget(probeSetNames, envir=envir, ifnotfound=list(NA)) ## this kind of thing could be included in 'multiget' as ## an extra feature. A function could be specified to ## process what is 'multi'-get on the fly for (i in seq(along=ans)) { if ( is.na(ans[[i]][1]) ) next ##as.vector cause it might be a matrix if all probe types tmp <- as.vector(ans[[i]][, i.probes]) ans[[i]] <- tmp } return(ans) } setMethod("indexProbes", signature("CdfEnvAffy", which = "character"), indexProbes.CdfEnvAffy) ## --- setGeneric("index2xy", def = function(object, ...) standardGeneric("index2xy")) setMethod("index2xy", signature(object="CdfEnvAffy"), function(object, ...) object@index2xy(object, ...)) ## --- setGeneric("xy2index", def = function(object, ...) standardGeneric("xy2index"), useAsDefault = FALSE) setMethod("xy2index", signature(object="CdfEnvAffy"), function(object, ...) object@xy2index(object, ...)) ## --- plot.CdfEnvAffy <- function(x, xlab = "", ylab = "", main = x@chipType, ...) { plot(0, 0, xlim = range(0, x@nrow), ylim = range(0, x@ncol), type="n", xlab = xlab, ylab = ylab, main = main, ...) } setMethod("plot", signature(x="CdfEnvAffy", y="missing"), plot.CdfEnvAffy) ## --- setMethod("show", signature("CdfEnvAffy"), function(object) { cat("Instance of class CdfEnvAffy:\n") cat(" name :", object@envName, "\n") cat(" chip-type:", object@chipType, "\n") cat(" size :", object@nrow, "x", object@ncol, "\n") cat("", length(ls(as(object, "environment"))), "probe set(s) defined.\n") }) ## --- validCdfEnvAffy <- function(cdfenv, verbose=TRUE) { if (verbose) cat("Validating CdfEnvAffy:\n") envir <- as(cdfenv, "environment") keys <- ls(envir) ## probe types if (verbose) cat(" Checking probe types.\n") n <- length(cdfenv@probeTypes) tmp <- rep(FALSE, n) for (i in seq(along=keys)) { if (ncol(get(keys[i], envir = envir)) != n) tmp[i] <- TRUE } if (n > 0 && sum(tmp) != 0) valid <- FALSE else valid <- TRUE r.probeTypes <- list(valid=valid, invalid.ones=keys[which(tmp)]) if (verbose) cat(sum(tmp), "invalid ones.\n") ## XY if (verbose) cat(" Checking XY coordinates.\n") tmp <- rep(FALSE, n) for (i in seq(along=keys)) { ip <- indexProbes(cdfenv, which = cdfenv@probeTypes, probeSetNames = keys[i])[[1]] xy <- index2xy(cdfenv, ip) if (any(xy[, 1] > cdfenv@nrow, na.rm = TRUE) || any(xy[, 2] > cdfenv@ncol, na.rm = TRUE)) tmp[i] <- TRUE } if (n > 0 && sum(tmp) != 0) valid <- FALSE else valid <- TRUE r.xy <- list(valid=valid, invalid.ones=keys[which(tmp)]) if (verbose) cat(sum(tmp), "invalid ones\n") r.details <- list(probeTypes=r.probeTypes, xy=r.xy) r <- all( unlist(lapply(r.details, function(x) x$valid)) ) attr(r, "details") <- r.details return(r) } ## --- printValidCdfEnvAffy <- function(x) { printDetails <- function(y) { if (y$valid) { cat(" valid.\n") return() } n <- length(y$invalid.ones) if (n == 1) cat(paste(" ", n, "invalid probe set\n")) else cat(paste(" ", n, "invalid probe sets\n")) if (n <= 5) cat(paste(y$invalid.ones, collapse=" "), "\n") else cat(paste(paste(y$invalid.ones[1:5], collapse=" "), "...\n")) } r.details <- attr(x, "details") cat("Probe types:\n") printDetails(r.details$probeTypes) cat("XY coordinates:\n") printDetails(r.details$xy) } ## --- validAffyBatch <- function(abatch, cdfenv) { stopifnot(is(abatch, "AffyBatch"), is(cdfenv, "CdfEnvAffy")) if ( (abatch@nrow != cdfenv@nrow) || (abatch@ncol != cdfenv@ncol)) valid <- FALSE else valid <- TRUE return(valid) #r.dim <- list(valid = valid) #return(r.dim) } ## --- # setMethod("initialize", "CdfEnvAffy", # function(.Object) { # }) altcdfenvs/R/appendCdfEnvAffy.R0000644000175200017520000000135614710217111017414 0ustar00biocbuildbiocbuildappendCdfEnvAffy <- function(acdfenv, id, i, nocopy=TRUE) { stopifnot(is.character(id), is.matrix(i), is.integer(i)) tmp.m <- match(colnames(i), acdfenv@probeTypes) if (! all(colnames(i) %in% acdfenv@probeTypes)) { stop("the CdfEnv only knows about probe types:\n", paste(acdfenv@probeTypes, collapse=",")) } if (exists(id, envir=acdfenv@envir)) { stop("'id' already in 'adfenv'") } if (! nocopy) { acdfenv <- copyCdfEnvAffy(acdfenv) } m <- matrix(as.integer(NA), nrow=nrow(i), ncol=length(acdfenv@probeTypes)) m[, tmp.m] <- i ##DEBUG: a consistency check (i.e., the index make sense given the ## geometry of the chip) would be nice... assign(id, m, envir=acdfenv@envir) return(acdfenv) } altcdfenvs/R/buildCdfEnv.biostrings.R0000644000175200017520000002102314710217111020611 0ustar00biocbuildbiocbuild mmProbes <- function(probes) { len_probe <- unique(nchar(probes$sequence)) if (length(len_probe) > 1) stop(paste("Different length for probes", "(and the handling of that case is not implemented).")) if (len_probe != 25) stop(paste("The expected probe length is 25 bp, not ", len_probe, ".", sep="")) mmpos <- 13 ## First write. Using DNAStringSet, short and elegant... ## but unfortunately unbearably slow ## mmseq <- ## lapply(as.list(probes$stringset), ## function(x) { ## replaceLetterAt(x, mmpos, ## as.character(complement(x[mmpos]))) ## }) pmprobe <- substr(probes$sequence, mmpos, mmpos) mmprobe <- rep(as.character(NA), length=length(pmprobe)) mmprobe[grep("[Aa]", pmprobe)] <- "T" mmprobe[grep("[Tt]", pmprobe)] <- "A" mmprobe[grep("[Gg]", pmprobe)] <- "C" mmprobe[grep("[Cc]", pmprobe)] <- "G" mmseq <- paste(substr(probes$sequence, 1, mmpos-1), mmprobe, substr(probes$sequence, mmpos+1, nchar(probes$sequence)), sep = "") return(mmseq) } setClass("AffyProbesMatch", representation(pm = "list", mm = "list", labels = "character", chip_type = "character", probes = "ANY"), # should be class "probetable" - S4 don't seem to cope with it validity = function(obj) { if (length(obj@pm) != length(obj@mm)) return("mm and pm should have identical lengths") if (length(obj@pm) != length(obj@labels)) return("labels and pm should have identical lengths") if (any(duplicated(obj@labels))) return("labels should be unique.") if (length(obj@chip_type) != 1) return("chip_type should be *one* chip type name") if (! all(unlist(lapply(obj@pm, function(y) inherits(y, "integer"))))) { return("all pm should inherit from numeric") } if (! all(unlist(lapply(obj@mm, function(y) inherits(y, "integer"))))) { return("all mm should inherit from numeric") } return(TRUE) }) setMethod("show", signature = c("AffyProbesMatch"), function(object) { cat("AffyProbesMatch:\n") cat(paste(length(object@pm), "target(s) sequences matched", "against", nrow(object@probes), "probes of chip type", object@chip_type, ".\n")) } ) setMethod("combine", signature = c("AffyProbesMatch", "AffyProbesMatch"), function(x, y, ...) { if (x@chip_type != y@chip_type) stop("Both 'chip_type' must be identical.") if (! identical(x@probes, y@probes)) stop("Both probe tables must be identical.") pm <- c(x@pm, y@pm) mm <- c(x@mm, y@mm) labels <- c(x@labels, y@labels) chip_type <- x@chip_type probetable <- x@probes res <- new("AffyProbesMatch", pm = pm, mm = mm, labels = labels, chip_type = chip_type, probes = probetable) return(res) }) toHypergraph <- function(object, ...) { stop("Not available for the given signature.") } setGeneric("toHypergraph") setMethod("toHypergraph", signature = c("AffyProbesMatch"), function(object, simplify=TRUE, ...) { if (simplify) { target_match <- unlist(lapply(object@pm, function(x) length(x) > 0)) probe_match <- rep(FALSE, length=nrow(object@probes)) for (i in which(target_match)) { probe_match[object@pm[[i]]] <- TRUE } } else { target_match <- rep(TRUE, length=length(object@pm)) probe_match <- rep(TRUE, length=nrow(object@probes)) } i_match <- rep(as.integer(NA), nrow(object@probes)) i_match[probe_match] <- seq(along=which(probe_match)) nodes <- paste(as.character(object@probes[["x"]][probe_match]), as.character(object@probes[["y"]][probe_match]), sep = "-") hEdges <- lapply(object@pm[target_match], function(x) Hyperedge(nodes[i_match[x]])) names(hEdges) <- object@labels[target_match] hg <- new("Hypergraph", nodes = nodes, hyperedges = hEdges) return(hg) } ) setMethod("toHypergraph", signature = c("CdfEnvAffy"), function(object, ...) { targets <- ls(object@envir) nodesEnv <- new.env(hash=TRUE, parent=emptyenv()) for (n in targets) { m <- object@envir[[n]] labels <- apply(index2xy(object, m[, 1]), 1, function(x) paste(x, collapse="-")) nodesEnv[[n]] <- labels } nodes <- unlist(as.list(nodesEnv), use.names=FALSE) nodes <- unique(nodes) hEdges <- lapply(nodesEnv, function(x) Hyperedge(x)) hg <- new("Hypergraph", nodes = nodes, hyperedges = hEdges) return(hg) }) matchAffyProbes <- function(probes, targets, chip_type, matchmm = TRUE, selectMatches = function(x) which(elementNROWS(x) > 0), ...) { if (! inherits(probes, "probetable")) { stop(paste("'probes' should inherit from class 'probetable'.")) } stringset <- DNAStringSet(probes$sequence) if (inherits(targets, "character")) { targets <- as.list(targets) for (ii in seq(along = targets)) { if (is.na(targets[[ii]])) { stop(paste("Target", ii, "is NA.")) } targets[[ii]] <- DNAString(targets[[ii]]) } } else if (inherits(targets, "list")) { for (ii in seq(along = targets)) { if (! inherits(targets[[ii]], "DNAString")) { stop("Invalid 'targets'.") } } } else if (! inherits(targets, "DNAString")) { stop("Invalid 'targets'.") } labels <- names(targets) if (is.null(labels)) { labels <- as.character(seq(along=targets)) } pmdict <- PDict(stringset) mindex_pm <- vector("list", length = length(targets)) for (ii in seq(along = targets)) { md <- matchPDict(pmdict, targets[[ii]], ...) mindex_pm[[ii]] <- selectMatches(md) } mindex_mm <- vector("list", length = length(targets)) if (matchmm) { mmseq <- mmProbes(probes) mmdict <- PDict(mmseq) for (ii in seq(along = targets)) { md <- matchPDict(mmdict, targets[[ii]], ...) mindex_mm[[ii]] <- selectMatches(md) } } apm <- new("AffyProbesMatch", pm = mindex_pm, mm = mindex_mm, labels = labels, chip_type = chip_type, probes=probes) return(apm) } buildCdfEnv.biostrings <- function(apm, abatch=NULL, nrow.chip=NULL, ncol.chip=NULL, simplify = TRUE, x.colname = "x", y.colname = "y", verbose = FALSE) { if (verbose) cat("validating 'apm'...") validObject(apm) if (verbose) cat("done.\n") if ( ! is.null(abatch)) { if (! is(abatch, "AffyBatch")) stop("abatch must be of class 'AffyBatch'.") nrow.chip <- abatch@nrow ncol.chip <- abatch@ncol chip_type <- abatch@cdfName } if (is.null(nrow.chip) || is.null(ncol.chip)) stop("nrow.chip, ncol.chip") probetab <- apm@probes cdfenv <- new.env(hash=TRUE) if (verbose) { cat("Processing the matches:\n") pbt <- new("ProgressBarText", length(apm@pm), barsteps = as.integer(20)) open(pbt) } ##FIXME: warning("Check index for MM probes.") for (i in seq(along = apm@pm)) { if (verbose) update(pbt) xy <- getxy.probeseq(probeseq = probetab, i.row = apm@pm[[i]], x.colname = x.colname, y.colname = y.colname) if (nrow(xy) == 0 && simplify) { next } assign(apm@labels[i], cbind(xy2indices(xy[, 1], xy[, 2], nc=nrow.chip), xy2indices(xy[, 1]+1, xy[, 2], nc=nrow.chip)), envir=cdfenv) } if (verbose) close(pbt) cdfenv <- wrapCdfEnvAffy(cdfenv, nrow.chip, ncol.chip, apm@chip_type) return(cdfenv) } altcdfenvs/R/buildCdfEnv.matchprobes.R0000644000175200017520000000372014710217111020741 0ustar00biocbuildbiocbuildbuildCdfEnv.matchprobes <- function(matches, ids, probes.pack, abatch=NULL, nrow.chip=NULL, ncol.chip=NULL, chiptype=NULL, mm=NA, simplify = TRUE, x.colname = "x", y.colname = "y", verbose = FALSE) { .Deprecated("buildCdfEnv.biostrings", package="altcdfenvs") if (! (is.list(matches) && length(matches) > 0)) #&& length(matches[[1]]) < 3) stop("arg 'matches' should be a list as returned by 'matchprobes'.") if (length(matches[[1]]) != length(ids)) stop("'matches' and 'ids' must have the same length.") if (length(matches[[1]]) != length(unique(ids))) stop("Some elements in 'ids' are not unique. You probably do not want this.") if ( ! is.null(abatch)) { if (! is(abatch, "AffyBatch")) stop("abatch must be of class 'AffyBatch'.") nrow.chip <- abatch@nrow ncol.chip <- abatch@ncol chiptype <- abatch@cdfName } if (is.null(nrow.chip) || is.null(ncol.chip) || is.null(chiptype)) stop("nrow.chip, ncol.chip or chiptype not defined.") do.call(library, list(probes.pack)) probe.tab <- get(probes.pack, envir=as.environment(paste("package:", probes.pack, sep=""))) cdfenv <- new.env(hash=TRUE) if (verbose) { cat("Processing the matches:\n") pbt <- new("ProgressBarText", length(matches$match), barsteps = as.integer(20)) open(pbt) } for (i in seq(along=matches$match)) { if (verbose) update(pbt) xy <- getxy.probeseq(probeseq=probe.tab, i.row=matches$match[[i]], x.colname = x.colname, y.colname = y.colname) if (nrow(xy) == 0 && simplify) { next } assign(ids[i], cbind(xy2indices(xy[, 1], xy[, 2], nc=nrow.chip), mm), envir=cdfenv) } if (verbose) close(pbt) cdfenv <- wrapCdfEnvAffy(cdfenv, nrow.chip, ncol.chip, chiptype) return(cdfenv) } altcdfenvs/R/cdfenvs.R0000644000175200017520000000304114710217111015672 0ustar00biocbuildbiocbuildwrapCdfEnvAffy <- function(cdfenv, nrow.chip, ncol.chip, chiptype, check = TRUE, verbose = FALSE) { object <- new("CdfEnvAffy", envir = cdfenv, envName = chiptype, nrow = as.integer(nrow.chip), ncol = as.integer(ncol.chip), probeTypes = c("pm", "mm"), chipType = chiptype) if (check) { valid <- validCdfEnvAffy(object, verbose=verbose) if ( ! valid ) { printValidCdfEnvAffy(valid) stop("invalid CdfEnvAffy") } } return(object) } getCdfEnvAffy <- function(abatch) { if (! is(abatch, "AffyBatch")) stop("arg must be of class 'AffyBatch'.") cdfenv <- getCdfInfo(abatch) cdfenv <- wrapCdfEnvAffy(cdfenv, abatch@nrow, abatch@ncol, abatch@cdfName) return(cdfenv) } getxy.probeseq <- function(ppset.id=NULL, probeseq=NULL, i.row=NULL, xy.offset=NULL, x.colname = "x", y.colname = "y") { if ( is.null(xy.offset) ) { xy.offset <- getOption("BioC")$affy$xy.offset } if (sum(c(is.null(ppset.id), is.null(i.row))) != 1) stop("specify one and only one of 'ppset.id', 'i.row'") if (is.null(probeseq)) stop("the argument 'probeseq' must be specified !") if (is.null(i.row)) i.row <- probeseq$Probe.Set.Name %in% ppset.id mm.offset <- rep(0, length=length(i.row)) mm.offset[i.row < 0] <- 1 i.row <- abs(i.row) xy <- cbind(probeseq[[x.colname]][i.row], probeseq[[y.colname]][i.row] + mm.offset) + xy.offset colnames(xy) <- c("x", "y") return(xy) } altcdfenvs/R/copyCdfEnvAffy.R0000644000175200017520000000015114710217111017107 0ustar00biocbuildbiocbuildcopyCdfEnvAffy <- function(acdfenv) { r <- acdfenv r@envir <- copyEnv(acdfenv@envir) return(r) } altcdfenvs/R/readFASTA.R0000644000175200017520000000776314710217111015753 0ustar00biocbuildbiocbuild## ## Set of (hopefully convenient) functions to extract ## sequences and headers from FASTA files ## ## Laurent 2003 - under LGPL license print.FASTA <- function(x, ...) { cat("FASTA sequence:\n", ...) if (is.null(x$header)) { cat(" NULL\n") } else { cat(paste(" ", substr(x$header, 1, 60), "...\n"), ...) cat(paste(" ", substr(x$sequence, 1, 60), "...\n"), ...) } } write.FASTA <- function(x, file="data.fasta", append = FALSE) { cat(x$header, file = file, "\n", sep = "", append = append) cat(x$sequence, file = file, "\n", sep = "", append = TRUE) } skip.FASTA.entry <- function(con, skip, linebreaks=3000) { ## skip FASTA entries in a connection for (i in rep(1, skip)) read.FASTA.entry(con, linebreaks=linebreaks) } read.n.FASTA.entries <- function(con, n, linebreaks=3000) { ## read n FASTA entries in a connection ## return a list of length n r.list <- vector("list", length=n) for (i in seq(along=r.list)) r.list[[i]] <- read.FASTA.entry(con) return(r.list) } read.n.FASTA.headers <- function(con, n, linebreaks=3000) { ## read n FASTA headers (skipping the sequences) in a connection ## return a vector of mode "character" of length n headers <- vector("character", length=n) for (i in seq(along=headers)) headers[i] <- read.FASTA.entry(con)$header return(headers) } read.n.FASTA.sequences <- function(con, n, linebreaks=3000) { ## read n FASTA sequences(skipping the headers) in a connection ## return a vector of mode character seqs <- vector("character", length=n) for (i in seq(along=seqs)) seqs[i] <- read.FASTA.entry(con)$sequence return(seqs) } read.n.FASTA.entries.split <- function(con, n, linebreaks=3000) { ## read n FASTA entries in a connection ## return a list of two elements: ## - a vector of headers ## - a vector of sequences headers <- vector("character", length=n) seqs <- vector("character", length=n) for (i in seq(along=seqs)) { fs <- read.FASTA.entry(con) headers[i] <- fs$header seqs[i] <- fs$sequence } r <- list(headers=headers, sequences=seqs) return(r) } countskip.FASTA.entries <- function(con, linebreaks=3000) { ## skip and count the remaining FASTA entries in a connection ## (handy to count the entries in a FASTA file) ## return an integer i <- as.integer(0) fs <- read.FASTA.entry(con) while(!identical(fs$header, character(0)) && !identical(fs$sequence, NULL)) { i <- i+1 fs <- read.FASTA.entry(con, linebreaks=linebreaks) } return(i) } read.FASTA.entry <- function(con, linebreaks=3000) { ## read the next FASTA entry in a connection ## (note: the parameters 'linebreaks' should be increased ## for very large sequences split in more than 'linebreaks' lines) ## return a list of two elements: ## - header: the FASTA header ## - sequence: the sequence getnext.FASTA.header <- function(con) { line <- readLines(con, n=1) while(length(line) > 0) { if (substr(line, 1, 1) == ">") { break } line <- readLines(con, n=1) } return(line) } bioseq <- vector("list", length=linebreaks) i <- as.integer(1) one.integer <- as.integer(1) header <- getnext.FASTA.header(con) line <- readLines(con, n=1) while(length(line) > 0) { if (substr(line, 1, 1) == ">") { pushBack(line, con) break } else { bioseq[[i]] <- line } i <- i + one.integer line <- readLines(con, n=1) } if (identical(header, character(0))) { header <- NULL bioseq <- NULL } else { bioseq <- paste(bioseq[1 : (i-1)], collapse="") } r <- list(header=header, sequence=bioseq) class(r) <- "FASTA" return(r) } grep.FASTA.entry <- function(pattern, con, ...) { ## grep the first FASTA entry with a header matching the pattern 'pattern' ## fs <- read.FASTA.entry(con) i <- 0 while (! identical(fs$header, NULL)) { i <- i + 1 if (length(grep(pattern, fs$header, ...)) > 0) break fs <- read.FASTA.entry(con) } attr(fs, "i") <- i return(fs) } altcdfenvs/R/removeIndex.R0000644000175200017520000000161714710217111016536 0ustar00biocbuildbiocbuildremoveIndex <- function(x, i, simplify = TRUE, verbose=FALSE) { if (! is.integer(i)) { stop("'i' must be of mode integer.") } remove.me <- rep(FALSE, length=max(i)) remove.me[i] <- TRUE tmp.env<- as(x, "environment") ids <- ls(tmp.env) ## copy env y <- new.env(hash=TRUE) if (verbose) cat("removing duplicated elements...") for (i in ids) { tmp.i <- get(i, envir=tmp.env) tmp.ok <- (c(tmp.i) > length(remove.me)) | (! remove.me[c(tmp.i)]) tmp.i[!tmp.ok] <- NA tmp.new <- tmp.i[!apply(tmp.i, 1, function(x) all(is.na(x))), , drop=FALSE] if (length(tmp.new) == 0 && simplify) { ##if (verbose) { ## cat(paste("removing ", i, " (does not have anymore elements).\n")) ##} next } assign(i, tmp.new, envir=y) } if (verbose) cat("done.\n") r <- x r@envir <- y r@envName <- paste(r@envName, "-removed", sep="") return(r) } altcdfenvs/R/unique.CdfEnvAffy.R0000644000175200017520000000364014710217111017527 0ustar00biocbuildbiocbuild##setGeneric("unique", function(x, incomparables, ...) standardGeneric("unique")) unique.CdfEnvAffy <- function(x, incomparables=FALSE, simplify=TRUE, verbose=FALSE, ...) { counts <- countduplicated(x, incomparables=incomparables, verbose=verbose) tmp.env<- as(x, "environment") ids <- ls(tmp.env) ## copy env y <- new.env(hash=TRUE) if (verbose) cat("removing duplicated elements...") for (i in ids) { tmp.count <- get(i, envir=counts) tmp.i <- get(i, envir=tmp.env) tmp.ok <- tmp.count == 1 tmp.i[!tmp.ok] <- NA tmp.new <- tmp.i[!apply(tmp.i, 1, function(x) all(is.na(x))), , drop=FALSE] if (length(tmp.new) == 0 && simplify) { ##if (verbose) { ## cat(paste("removing ", i, " (does not have anymore elements).\n")) ##} next } assign(i, tmp.new, envir=y) } if (verbose) cat("done.\n") r <- x r@envir <- y r@envName <- paste(r@envName, "-unique", sep="") return(r) } ##setMethod("unique", signature(x="CdfEnvAffy", incomparables="logical"), .unique.CdfEnvAffy) countduplicated <- function(x, incomparables=FALSE, verbose=FALSE) { if (!is(x, "CdfEnvAffy")) stop("x must inherit from 'CdfEnvAffy'") if (incomparables != FALSE) warning("'incomparable' not yet implemented !") if (verbose) cat("Initialize...") tmp.env <- as(x, "environment") ids <- ls(tmp.env) p.type <- x@probeTypes tmp.count <- rep(as.integer(0), length=sum(unlist(lapply(indexProbes(x, p.type), length)))) r <- new.env(hash = TRUE) if(verbose) cat("done.\nCounting probes...") for (i in seq(along = ids)) { p.i <- get(ids[i], envir = tmp.env) tmp.count[p.i] <- tmp.count[p.i] + 1 } if (verbose) cat("done.\nAssigning counts...") for (i in seq(along = ids)) { p.i <- get(ids[i], envir = tmp.env) p.i[] <- tmp.count[p.i] assign(ids[i], p.i, envir=r) } if (verbose) cat("done.\n") return(r) } altcdfenvs/build/0000755000175200017520000000000014710267404015031 5ustar00biocbuildbiocbuildaltcdfenvs/build/vignette.rds0000644000175200017520000000051114710267404017365 0ustar00biocbuildbiocbuildR=O0uPڈ0P 1ZɹX$vd[m!\Z)Đ'G1>~uA29lrK=˕C\-J.@L&-u_( 9qrAa-iL"9HkU4g@dV,'G8+M1Jͭn=s;s}/t6a:W_tChJyBA eV5dh;0E E؟7./OPL1xr4 ZEez UU}v'J2f\Me؏7W{AFaltcdfenvs/data/0000755000175200017520000000000014710217111014631 5ustar00biocbuildbiocbuildaltcdfenvs/data/cdfenvEx.rda0000644000175200017520000000156114710217111017066 0ustar00biocbuildbiocbuilduUMI w UāY@i\0$( h> 3a搏v^U隘pMl%QN\)SIhy?ޝVaX7݉O7bz˿<[ԏ1B2y=h/Cdns0LtHJ,s+~M4QRӸawm̟CjuǜNju莏=3x:H%#h;=;OTLec>h䄢&1B9/X$;JJMm4Nƒ)e}F%Xẍ́fدHʠ= dj1r& AOہ4J\5j3*EK%m &jJ9<؞U6P#T#檐 RA b?8e!T|Y` *ж x d`+R CT40\`i/4fcŘ= q`6CS,X\gZ \C_茕p;DLCQ RðXq PH9[1hH*/ 8\ ( fZ \H VVj `& d : 9 FW`0 P!v@˖ GnüpũhAkLyD/P,s`!ST#'\ 0b&73y _kUtF_(gw<(wK|9^gwKy{1>\n]>nYfcY>nPzq?:)zaltcdfenvs/inst/0000755000175200017520000000000014710267404014707 5ustar00biocbuildbiocbuildaltcdfenvs/inst/CITATION0000644000175200017520000000102214710217111016025 0ustar00biocbuildbiocbuildcitEntry(entry = "Article", "author" = "Laurent Gautier and Morten Mooller and Lennart Friis-Hansen and Steen Knudsen", "title" = "Alternative mapping of probes to genes for {\\it Affymetrix} chips", journal = "BMC Bioinformatics", year = "2004", note = "5:111 (14 August 2004)", textVersion = "Alternative mapping of probes to genes for Affymetrix chips Laurent Gautier, Morten Mooller, Lennart Friis-Hansen, Steen Knudsen BMC Bioinformatics 2004, 5:111 (14 August 2004)" ) altcdfenvs/inst/UnitTests/0000755000175200017520000000000014710217111016637 5ustar00biocbuildbiocbuildaltcdfenvs/inst/UnitTests/AffyProbesMatch_test.R0000644000175200017520000000360214710217111023037 0ustar00biocbuildbiocbuild library(RUnit) library(altcdfenvs) pm_1 <- "AATAATAATAATAATAATAATAAGC" mm_1 <- "AATAATAATAATTATAATAATAAGC" pm_2 <- "CCACCACCACCACCACCACCACCTG" mm_2 <- "CCACCACCACCAGCACCACCACCTG" pm_3 <- "GGAGGGAGGGAGGGAGGGAGGGACT" mm_3 <- "GGAGGGAGGGAGCGAGGGAGGGACT" pm_4 <- "TTATTATTATTATTATTATTATTGC" mm_4 <- "TTATTATTATTAATATTATTATTGC" probetable <- data.frame(sequence = I(c(pm_1, pm_2, pm_3, pm_4)), x = c(10, 11, 13, 13), y = c(10, 12, 11, 12), Probe.Set.Name = I(c("12_at", "12_at", "m4_at", "4_at")), Probe.interrogation.Position = c(100, 120, 130, 140), Target.Strandeness = factor(rep("Antisense", 4))) class(probetable) <- c("data.frame", "probetable") ## test mmProbe mmp <- mmProbes(probetable) checkIdentical(c(mm_1, mm_2, mm_3, mm_4), mmp) target_1 <- paste(pm_1, pm_2, sep="GCGCG") target_2 <- paste(pm_1, pm_4, sep="GCGCG") target_3 <- paste("GGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG", mm_3, sep="") targets <- list(t1 = DNAString(target_1), t2 = DNAString(target_2), t3 = DNAString(target_3)) ## test match apm <- matchAffyProbes(probetable, targets, chip_type = "foo") checkIdentical(apm@pm[[1]], as.integer(c(1,2))) checkIdentical(apm@pm[[2]], as.integer(c(1,4))) checkIdentical(apm@pm[[3]], integer(0)) checkIdentical(apm@mm[[2]], integer(0)) checkIdentical(apm@mm[[3]], as.integer(c(3))) ## test merge checkIdentical(combine(matchAffyProbes(probetable, targets[1:2], "foo"), matchAffyProbes(probetable, targets[3], "foo")), matchAffyProbes(probetable, targets, "foo")) ## toHypergraph hg <- toHypergraph(apm) ## test build env altCdf <- buildCdfEnv.biostrings(apm, nrow.chip = 15, ncol.chip = 15) ## checkIdentical(hg, toHypergraph(altCdf)) altenv <- as(altCdf, "environment") # cdfenv <- new.env(hash = TRUE, parent=emptyenv()) altcdfenvs/inst/doc/0000755000175200017520000000000014710267404015454 5ustar00biocbuildbiocbuildaltcdfenvs/inst/doc/altcdfenvs.R0000644000175200017520000001225314710267366017742 0ustar00biocbuildbiocbuild### R code from vignette source 'altcdfenvs.Rnw' ################################################### ### code chunk number 1: altcdfenvs.Rnw:71-72 ################################################### library(altcdfenvs) ################################################### ### code chunk number 2: altcdfenvs.Rnw:91-94 ################################################### fasta.filename <- system.file("exampleData", "sample.fasta", package="altcdfenvs") con <- file(fasta.filename, open="r") ################################################### ### code chunk number 3: altcdfenvs.Rnw:99-105 ################################################### fasta.seq <- read.FASTA.entry(con) while(! is.null(fasta.seq$header)) { print(fasta.seq) fasta.seq <- read.FASTA.entry(con) } close(con) ################################################### ### code chunk number 4: altcdfenvs.Rnw:127-136 ################################################### ## first, count the number of FASTA entries in our file con <- file(fasta.filename, open="r") n <- countskip.FASTA.entries(con) close(con) ## read all the entries con <- file(fasta.filename, open="r") my.entries <- read.n.FASTA.entries.split(con, n) close(con) ################################################### ### code chunk number 5: altcdfenvs.Rnw:149-151 ################################################### library(hgu133aprobe) ################################################### ### code chunk number 6: altcdfenvs.Rnw:156-164 ################################################### targets <- my.entries$sequences names(targets) <- sub(">.+\\|(Hs\\#|NM_)([^[:blank:]\\|]+).+", "\\1\\2", my.entries$headers) m <- matchAffyProbes(hgu133aprobe, targets, "HG-U133A") ################################################### ### code chunk number 7: altcdfenvs.Rnw:175-176 ################################################### hg <- toHypergraph(m) ################################################### ### code chunk number 8: altcdfenvs.Rnw:182-183 ################################################### gn <- toGraphNEL(hg) ################################################### ### code chunk number 9: altcdfenvs.Rnw:190-194 ################################################### targetNodes <- new.env(hash=TRUE, parent=emptyenv()) for (i in seq(along=targets)) { targetNodes[[names(targets)[i]]] <- i } ################################################### ### code chunk number 10: plotGraph ################################################### library(Rgraphviz) tShapes <- rep("ellipse", length=length(targets)) names(tShapes) <- names(targets) tColors <- rep("ivory", length=length(targets)) names(tColors) <- names(targets) nAttrs <- list(shape = tShapes, fillcolor = tColors) gAttrs <- list(node = list(shape = "rectangle", fixedsize = FALSE)) plot(gn, "neato", nodeAttrs = nAttrs, attrs = gAttrs) ################################################### ### code chunk number 11: buildCdfEnv ################################################### alt.cdf <- buildCdfEnv.biostrings(m, nrow.chip = 712, ncol.chip = 712) ################################################### ### code chunk number 12: geneSymbolsSLAMF ################################################### geneSymbols <- c("SLAMF1", "SLAMF3", "SLAMF6", "SLAMF7", "SLAMF8", "SLAMF9") ################################################### ### code chunk number 13: getSeq ################################################### getSeq <- function(name) { seq <- getSequence(id=name, type="hgnc_symbol", seqType="cdna", mart = mart) targets <- seq$cdna if (is.null(targets)) return(character(0)) names(targets) <- paste(seq$hgnc_symbol, 1:nrow(seq), sep="-") return(targets) } ################################################### ### code chunk number 14: loadTargetsSLAMF ################################################### load(system.file("exampleData", "slamf_targets.RData", package="altcdfenvs")) ################################################### ### code chunk number 15: altcdfenvs.Rnw:322-323 ################################################### m <- matchAffyProbes(hgu133aprobe, targets, "HG-U133A") ################################################### ### code chunk number 16: SLAMF ################################################### hg <- toHypergraph(m) gn <- toGraphNEL(hg) library(RColorBrewer) col <- brewer.pal(length(geneSymbols)+1, "Set1") tColors <- rep(col[length(col)], length=numNodes(gn)) names(tColors) <- nodes(gn) for (col_i in 1:(length(col)-1)) { node_i <- grep(paste("^", geneSymbols[col_i], "-", sep=""), names(tColors)) tColors[node_i] <- col[col_i] } nAttrs <- list(fillcolor = tColors) plot(gn, "twopi", nodeAttrs=nAttrs) ################################################### ### code chunk number 17: altcdfenvs.Rnw:362-371 ################################################### library("hgu133a.db") affyTab <- toTable(hgu133aSYMBOL) slamf_i <- grep("^SLAMF", affyTab$symbol) pset_id <- affyTab$probe_id[slamf_i] library("hgu133acdf") countProbes <- lapply(pset_id, function(x) nrow(hgu133acdf[[x]])) names(countProbes) <- affyTab$symbol[slamf_i] countProbes altcdfenvs/inst/doc/altcdfenvs.Rnw0000644000175200017520000002546014710217111020272 0ustar00biocbuildbiocbuild% -*- mode: noweb; noweb-default-code-mode: R-mode; -*- %\VignetteIndexEntry{altcdfenvs} %\VignetteKeywords{Preprocessing, Affymetrix} %\VignetteDepends{altcdfenvs} %\VignettePackage{altcdfenvs} \documentclass[12pt]{article} %\usepackage{amsmath} %\usepackage{hyperref} \usepackage[authoryear,round]{natbib} \textwidth=6.2in \textheight=8.5in %\parskip=.3cm \oddsidemargin=.1in \evensidemargin=.1in \headheight=-.3in \newcommand{\scscst}{\scriptscriptstyle} \newcommand{\scst}{\scriptstyle} \newcommand{\Rfunction}[1]{{\texttt{#1}}} \newcommand{\Robject}[1]{{\texttt{#1}}} \newcommand{\Rclass}[1]{{\texttt{#1}}} \newcommand{\Rpackage}[1]{{\textit{#1}}} \author{Laurent Gautier} \title{Alternative CDF environments} \begin{document} \maketitle \tableofcontents \section{Introduction} On short oligonuleotide arrays, several probes are designed to match a target transcript, and probes matching the same target transcript can be grouped in a probe set. Between the time the probes for a given short oligonucleotide chip were designed, and the time an analysis is made, the knowledge of expected transcripts for a given organism might have changed. Unless one includes the latest development in transcripts into an analysis, the analysis could suffer from what we like to call a {\it Dorian Gray}\footnote{From the novel `The Picture of Dorian Gray' by Oscar Wilde.} effect. The chip itself does not change, which means that the probes and their respective sequences remain the same, while the knowledge of the transcripts, and eventually their sequence, might evolve, and in time the immobility of the probe and probe sets give an uglier picture of the biological phenomena to study. Being able to easily modify or replace the grouping of probes in probe sets gives the opportunity to minimize this effect. The package is directly usable with {\it Affymetrix} {\it GeneChip} short oligonucleotide arrays, and can be adapted or extended to other platforms. The bibliographic reference associated with the package is given by the command: \begin{Scode} citation(package="altcdfenvs") \end{Scode} \begin{quote} Alternative mapping of probes to genes for Affymetrix chips Laurent Gautier, Morten Mooller, Lennart Friis-Hansen, Steen Knudsen BMC Bioinformatics 2004, 5:111 \end{quote} If you use it, consider citing it, and if you cite it consider citing as well other packages it depends on. To start we will first load the package: <<>>= library(altcdfenvs) @ \section{The class \Rclass{CdfEnvAffy}} Each instance of this class contains a way to group probes in probe sets. Different instances, describing different ways to group probes in probe sets, can co-exist for a given chip type. When experimenting, it is highly recommended to use the functions \Rfunction{validCdfEnvAffy} and \Rfunction{validAffyBatch} to make sure that a given instance is a valid one. \section{Reading sequence information in FASTA connections} The package contains simple functions to read {\bf R} connections in the FASTA format. Typically, collections of sequences are stored in FASTA files, which can be significantly large, one can wish to read and process sequences one after the other. This can be done by opening the file in `r' mode: <<>>= fasta.filename <- system.file("exampleData", "sample.fasta", package="altcdfenvs") con <- file(fasta.filename, open="r") @ Reading the sequences one after another, and printing information about them in turn goes like: <<>>= fasta.seq <- read.FASTA.entry(con) while(! is.null(fasta.seq$header)) { print(fasta.seq) fasta.seq <- read.FASTA.entry(con) } close(con) @ One can foresee that the matching of a set of reference sequences against all the probes can be parallelized easily: the reference sequences can simply be distributed across different processors/machines. When working with all the reference sequences in a single large FASTA file, the option \Robject{skip} can let one implement a poor man's parallel sequence matching very easily. \section{Creating an alternative mapping from sequences in a FASTA file} \subsection{Select the constituting elements} \begin{itemize} \item Chip type: For this tutorial we decide to work with the Affymetrix chip HG-U133A. \item Target sequences: The set of target sequences we use for this tutorial is in the exemplar FASTA file: <<>>= ## first, count the number of FASTA entries in our file con <- file(fasta.filename, open="r") n <- countskip.FASTA.entries(con) close(con) ## read all the entries con <- file(fasta.filename, open="r") my.entries <- read.n.FASTA.entries.split(con, n) close(con) @ \end{itemize} \subsection*{matching the probes} The package \Rpackage{Biostrings} and the probe data package for HG-U133A are required to perform the matching. The first step is to load them: <<>>= library(hgu133aprobe) @ The matching is done simply (one can refer to the documentation for the package \Rpackage{Biostrings} for further details): <<>>= targets <- my.entries$sequences names(targets) <- sub(">.+\\|(Hs\\#|NM_)([^[:blank:]\\|]+).+", "\\1\\2", my.entries$headers) m <- matchAffyProbes(hgu133aprobe, targets, "HG-U133A") @ \subsection{analyzing the matches} When the position of the match between probes and target sequences does not matter, the association can be represented as a bipartite graph. The method \Rfunction{toHypergraph} will transform an instance of \Rclass{AffyProbesMatch} into an \Rclass{Hypergraph}. <<>>= hg <- toHypergraph(m) @ Currently, there are not many functions implemented around hypergraphs, so we convert it to a more common graph. <<>>= gn <- toGraphNEL(hg) @ Since this is now a regular graph, all of probes and targets are regular nodes on that graph. Node name-based rules can be applied to identify whether a node is a target sequence or a probe. <<>>= targetNodes <- new.env(hash=TRUE, parent=emptyenv()) for (i in seq(along=targets)) { targetNodes[[names(targets)[i]]] <- i } @ Since the graph is relatively small, we can plot it, and see that one probe is common to both probe sets: <>= library(Rgraphviz) tShapes <- rep("ellipse", length=length(targets)) names(tShapes) <- names(targets) tColors <- rep("ivory", length=length(targets)) names(tColors) <- names(targets) nAttrs <- list(shape = tShapes, fillcolor = tColors) gAttrs <- list(node = list(shape = "rectangle", fixedsize = FALSE)) plot(gn, "neato", nodeAttrs = nAttrs, attrs = gAttrs) @ Whenever a large number oftarget sequences are involved, counting the degrees will be more efficient than plotting. The package contains a function to create a \Rclass{CdfEnv} from the matches: <>= alt.cdf <- buildCdfEnv.biostrings(m, nrow.chip = 712, ncol.chip = 712) @ Note that the size for chip must be specified. This is currently a problem with cdfenvs as they are created by the package \Rpackage{makecdfenv}. The class \Rclass{CdfEnv} suggests a way to solve this (hopefully this will be integrated in \Rpackage{makecdfenv} in the near future). When this happens, the section below will be replaced by something more intuitive. But in the meanwhile, here is the current way to use our shiny brand new class \Rclass{CdfEnv}: \begin{Scode} ## say we have an AffyBatch of HG-U133A chips called 'abatch' ## summary checks to avoid silly mistakes validAffyBatch(abatch, alt.cdf) ## it is ok, so we proceed... ## get the environment out of it class alt.cdfenv <- alt.cdf@envir abatch@cdfName <- "alt.cdfenv" \end{Scode} From now on, the object \Robject{abatch} will use our `alternative mapping' rather than the one provided by the manufacturer of the chip: \begin{Scode} print(abatch) \end{Scode} %\section*{Creating an alternative environment to store only perfect matches} \section{Always up-to-date} Even if alternative mapping is not used upstream of the analysis, it can still be interesting to verify probesets highlighted during data analysis. The \Rpackage{biomaRt} package makes withdrawing up-to-date sequences very easy, and those sequences can be matched against the probes. First, we create a \emph{mart}: \begin{Scode} library(biomaRt) mart <- useMart("ensembl",dataset="hsapiens_gene_ensembl") \end{Scode} (refer to the documentation for the \Rpackage{biomaRt} for further information). \subsection{Casual checking of genes} In this example, we assume that for one reason or an other a researcher would like to know more about the probes matching the SLAMF genes. <>= geneSymbols <- c("SLAMF1", "SLAMF3", "SLAMF6", "SLAMF7", "SLAMF8", "SLAMF9") @ The vector \Robject{geneSymbols} defined can easily be replaced by your favorite genes; the example below should still work. We then write a convenience function \Robject{getSeq} to extract the sequences. This function appenda a \verb+-+ to the HUGO symbol (as there might be several sequences matching). <>= getSeq <- function(name) { seq <- getSequence(id=name, type="hgnc_symbol", seqType="cdna", mart = mart) targets <- seq$cdna if (is.null(targets)) return(character(0)) names(targets) <- paste(seq$hgnc_symbol, 1:nrow(seq), sep="-") return(targets) } @ % load saved data (instead of connecting to the mart) <>= load(system.file("exampleData", "slamf_targets.RData", package="altcdfenvs")) @ The function let us obtain the target sequences very easily: \begin{Scode} targets <- unlist(lapply(geneSymbols, getSeq)) \end{Scode} The targets are matched as seen previously: <<>>= m <- matchAffyProbes(hgu133aprobe, targets, "HG-U133A") @ A colorful graph can be made in order to visualize how matching probes are distributed: <>= hg <- toHypergraph(m) gn <- toGraphNEL(hg) library(RColorBrewer) col <- brewer.pal(length(geneSymbols)+1, "Set1") tColors <- rep(col[length(col)], length=numNodes(gn)) names(tColors) <- nodes(gn) for (col_i in 1:(length(col)-1)) { node_i <- grep(paste("^", geneSymbols[col_i], "-", sep=""), names(tColors)) tColors[node_i] <- col[col_i] } nAttrs <- list(fillcolor = tColors) plot(gn, "twopi", nodeAttrs=nAttrs) @ \begin{itemize} \item Watch for \emph{SLAMF6} and \emph{SLAMF7} \item The second sequence in SLAMF8 can potentially has specific probes (the rest of the probes are matching both SLAMF8 sequences) \end{itemize} Comparison with the official mapping can be made (not so simply, a future version should address this) <<>>= library("hgu133a.db") affyTab <- toTable(hgu133aSYMBOL) slamf_i <- grep("^SLAMF", affyTab$symbol) pset_id <- affyTab$probe_id[slamf_i] library("hgu133acdf") countProbes <- lapply(pset_id, function(x) nrow(hgu133acdf[[x]])) names(countProbes) <- affyTab$symbol[slamf_i] countProbes @ The results do not appear in complete agreement with the matching just performed. \end{document} altcdfenvs/inst/doc/altcdfenvs.pdf0000644000175200017520000110542114710267366020313 0ustar00biocbuildbiocbuild%PDF-1.5 % 3 0 obj << /Length 1763 /Filter /FlateDecode >> stream xXK6ЭVDJ&hQ mEir%&KI83JNCS97#>^O@đ" ϓ(I 2J2xh>B2ndwqR0'cyƐ!ë4x%Ƚ"IM&K,FshFDO`ȣ2ڼ)ܠ&) &k"H LRṈx3͂.Lb6jfe9˜1(pSƒ}G(9/*N<: "|ܣUfZ`.$@N*7ݧxID&l,c)DNUm0?'U^#m{*6h9cXƫwvV auJRXSR:[۷)YpٙI `R=)eG[R:(8f#sE&`0q-Ff1M \xV r-Wj_+!?Lc$X|;K9#6sn:i1g}NNoj5jKӌ˖Sähh7|\Boic +xMn,+E/ҡo7^_[B@eveߘЃF5+kkBp-FoCPz0N׸JzmN{]F0^_zs,9_$]8V{MwI_Iu:xht A^הW} xA7⛊݂@ vpd)+s6s[aMKG-LlN 9Њ^;:dUϚys,e9UvΡcףrύw~ 7{5*d%9&爂Nufh|ۣ#-.ARN.%k0Pw&$jLayN\tjZVO+#ֵ{4N`OMSh#&h `nK{5e6#yɭP#U5 (z ̷f{kІT`Ch<69R,*夘!Q&%ykڙUᛓ.U;9lA7[jnjry_Y EGR-'3Zu߈D# ϟ/nKtV/ztV |m8,ؽ|yy*NIljxGψ9 9.hR*{5 @"H'uq$q3jbfڶ2q0{CjVN Sth =lFՙv]cWҚj^D~5М?w&e=ӝ[8S} ^jks3R4h5ɵRoC*W.*.ozܠpD)סZM*|қݙ|3=Qi.w( ΃2RvW&8F;\Mzj<ЍybFњDϥ8/sU'*U+F]\LٚU`wjupz7~Z!V.Ba<8G_yqDPQ\j 쮵ü ]|u@$>"8 Ke9g})[`'>9C#9I| _qi&)e7l Ӝ0;T7:_ 2]ك ޞc endstream endobj 18 0 obj << /Length 1596 /Filter /FlateDecode >> stream xڕWnF}WB~ v$\ S]{粔HU.'fgggfϜݬ.^FexEH,).~ů5eUA/`+`{ ˼ukЁEvb"g#[խG`j^n"5+7ֲEu?E4zb Q[͇ދde;p_>~0 59ѷ-*(wރ8 gPJ/Ud$J_]G7؅Ul 39CWɫ Fe~jSϘ$Gi e0iUIL`3BZy-[p`BhhnzZBжBޘcmw;1'w\yІ_JQ<} &m+uw?>,d$@ɁU"g'rОQU%kPHL/4R6jqC?@9s\xyAQ0p+n*(DA::9\ds W\- A9c3 l|6+.~ P6q)@pXK<6jdp$:"j!ŸoϱN+D>G^QV4ZD~DF[p N d2c3ҙ royi7AT;o{~>jNl$˾_mhǂ|Xo+^hyh ى 6)b'#9ܺU> stream xڵ[ko#ub  q~8玃:Ȗ jQRBlO0?>u9Imǎa Gꪺu>-K݇x<\7r=Yը߽~msמn~,fv<f 6}?v> [ߍ|`cx[џ|t~tGg>Io/Tp=g}}:oN}z|S5:CLwχc}?=w>a4n~wu#qٗXڟ^o*iWӮ= FI=lZ>xGjc{o~?u<ڽLb6ғ4nt9~?Y W됋s~-KFJ9TJX%U*֒ՆJK MO)HUTwjY|TkKJ^1O 2^죢O1i HInc[P]}Mc*?5IQ88%>e֟ә*bIB@8mhu·L9cT4'{(crA|\/ ye$$wj1@VrܣH[ ^`>Es}eI\Go'32¥=bw>DRyzi'gx@3~ci BOebӟULKT'!E9C'JL(ػq9f%@x>E(\D)16 P3r,ILY&r{e[W|l@1 Uw;$D)H<v-Xbڲ" I~Sp|Ʉ`/m ,fN$ &pV.?hP_ 4UP8d)hs)qE%>XPxI8GlX+ "LG I18Ҕnl*)+;èһ[ReM -!m(Y0$Tb$Nf@bț|SH6Y '):,0H"i.vMLIr P5)tkj)ufFзȖ"ҝp/6GRk2RXF'dh`o\0avMvMWJz&40zY1Nef Z`)*gBȄBLCbf9d W (# [ hK TG gr)%F̼y R`h%z5ki) rh9!fz.ըY_kxs9zGJ fl*+V@A f }TZ B 0ʊ|2C^,Eh mHSa0LLQH"+$|Sõk$TI'W qL>X1q}ȉQ SoLX2cyE.ȚDÚ2btA/JU` DtL-q22چXMܷk dzd4͌o=1(!DkBVDQ98Thۯ7| `"Zw2;! 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If you do not know these numbers for your chip, the easiest (for the moment) is to read CEL data in an \Rclass{AffyBatch} and call the function \Rfunction{print} on this object. Hopefully, the cdf packages offered on the bioconductor website will be modified, which will make this step (and the complication to know the dimension of the chip) unncessary. \section*{How to subset an environment using probe set ids} (see the vignette `n-genomes chips') \section*{How to work with given index / XY coordinates} \subsection*{Getting index} The method \Rfunction{indexProbes} is implemeted for objects of class \Rclass{AltCdfEnvs} <<>>= #indexProbes(planocdf, "pm", "") @ One can directly work on the CDF data, without having to load CEL data. \subsection*{Removing probe sets} The function \Rfunction{removeIndex} let one remove probe sets given their index. \subsection*{Multiple use of index} When crafting an AltCdfEnv, it can happen that probe indexes are used by several probe sets. 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If you do not know these numbers for your chip, the easiest (for the moment) is to read CEL data in an \Rclass{AffyBatch} and call the function \Rfunction{print} on this object. \section*{How to create a CdfEnvAffy that is a subset of the 2-genomes one} If the identifiers starting with `Pf' correspond to plasmodium, it is an easy job to find them: <<>>= ids <- geneNames(planocdf) ids.pf <- ids[grep("^Pf", ids)] @ Subsetting the \Rclass{CdfEnvAffy} is also an easy task: <<>>= ## subset the object to only keep probe sets of interest plcdf <- planocdf[ids.pf] print(plcdf) @ However, this is not that simple:{\bf the environment created does not contain all the probe set ids from Plasmodium}. Unfortunately, one cannot rely on pattern matching on the probe set id to find all the probe set ids associated with Plasmodium. The list of plasmodium ids included in the package can let us build a Plasmodium-only CdfEnvAffy (contributed by Zhining Wang). <<>>= filename <- system.file("exampleData", "Plasmodium-Probeset-IDs.txt", package="altcdfenvs") ids.pf <- scan(file = filename, what = "") plcdf <- planocdf[ids.pf] print(plcdf) @ Before we eventually save our environment, we may want to give it an explicit name: <<>>= plcdf@envName <- "Plasmodium ids only" print(plcdf) @ \section*{Assign the new Cdf data to an AffyBatch} Handling of AffyCdfEnv directly in within an AffyBatch, or AffyBatch-like, structure is being completed\ldots in the meanwhile, the current mecanism for cdfenvs has to be used. If your CEL files were read into an AffyBatch named \Robject{abatch}. \begin{Scode} envplcdf <- as(plcdf, "environment") abatch@cdfName <- "plcdf" \end{Scode} From now on, \Robject{abatch} will only consider Cdf information from \Robject{plcdf}. 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Pf.9.89.0_CDS_at Pf.9.91.0_CDS_at Pf.9.93.0_CDS_at Pf.9.94.0_CDS_at Pf.9.95.0_CDS_at Pf.9.96.0_CDS_at Pf.9.98.1_a_at Pf.9.99.1_a_at Pf.UN_1.3.0_CDS_at Pf.UN_1.4.0_CDS_at Pf.UN_2.5.0_CDS_at Pf.UN_3.6.0_CDS_at Pf.UN_4.1.0_CDS_at Pf.UN_4.10.0_CDS_at Pf.UN_4.11.0_CDS_x_at Pf.UN_4.2.0_CDS_at Pf.UN_4.7.0_CDS_at Pf.UN_4.8.0_CDS_at Pf.UN_4.9.0_CDS_x_at Pfa3D7_hrpIII_at Pfa3D7_hrpIII_x_at Pfa3D7_hrpII_at Pfa3D7_hrpII_x_at U09839.1_s_at U27339.1_at U60602.1_at U60603.1_x_at U82507.1_RC_x_at U82507.1_x_at U82508.1_s_at U82509.1_x_at X00245.1_RC_x_at X00245.1_x_at X02406.1_RC_s_at X02406.1_s_at X03144.1_at X13014.1_RC_at X15063.1_RC_at X15063.1_RC_x_at X17483.1_s_at X17484.1_s_at X17486.1_RC_at X17486.1_s_at X71408.1_s_at X71409.1_at X87840.1_s_at Y09693.1_RC_at Y09693.1_s_at Y13404.1_at Y13404.1_RC_at Y13404.1_RC_x_at Y13404.1_x_at Y13405.1_at Y13405.1_RC_at Y13405.1_s_at Y13405.1_x_at Y13406.1_RC_at Y13406.1_s_at Y13406.1_x_at Y13407.1_at Y13407.1_RC_at Y13408.1_at altcdfenvs/inst/exampleData/sample.fasta0000644000175200017520000002441214710217111021426 0ustar00biocbuildbiocbuild>gnl|UG|Hs#S1730546 membrane-spanning 4-domains, subfamily A, member 2; Fc epsilon receptor I beta-chain; immunoglobulin E receptor, high affinity, beta polypeptide; Fc IgE receptor, beta chain [Homo sapiens], mRNA sequence /cds=(102,836) /gb=NM_000139 /gi=23397640 /ug=Hs.30 /len=3723 AACCCATTTCAACTGCCTATTCAGAGCATGCAGTAAGAGGAAATCCACCAAGTCTCAATATAATAATATTCTTTATTCCTGGACAGCTCGGTTAATGAAAAAATGGACACAGAAAGTAATAGGAGAGCAAATCTTGCTCTCCCACAGGAGCCTTCCAGTGTGCCTGCATTTGAAGTCTTGGAAATATCTCCCCAGGAAGTATCTTCAGGCAGACTATTGAAGTCGGCCTCATCCCCACCACTGCATACATGGCTGACAGTTTTGAAAAAAGAGCAGGAGTTCCTGGGGGTAACACAAATTCTGACTGCTATGATATGCCTTTGTTTTGGAACAGTTGTCTGCTCTGTACTTGATATTTCACACATTGAGGGAGACATTTTTTCATCATTTAAAGCAGGTTATCCATTCTGGGGAGCCATATTTTTTTCTATTTCTGGAATGTTGTCAATTATATCTGAAAGGAGAAATGCAACATATCTGGTGAGAGGAAGCCTGGGAGCAAACACTGCCAGCAGCATAGCTGGGGGAACGGGAATTACCATCCTGATCATCAACCTGAAGAAGAGCTTGGCCTATATCCACATCCACAGTTGCCAGAAATTTTTTGAGACCAAGTGCTTTATGGCTTCCTTTTCCACTGAAATTGTAGTGATGATGCTGTTTCTCACCATTCTGGGACTTGGTAGTGCTGTGTCACTCACAATCTGTGGAGCTGGGGAAGAACTCAAAGGAAACAAGGTTCCAGAGGATCGTGTTTATGAAGAATTAAACATATATTCAGCTACTTACAGTGAGTTGGAAGACCCAGGGGAAATGTCTCCTCCCATTGATTTATAAGAATCACGTGTCCAGAACACTCTGATTCACAGCCAAGGATCCAGAAGGCCAAGGTCTTGTTAAGGGGCTACTGGAAAAATTTCTATTCTCTCCACAGCCTGCTGGTTTTACATTAGATTTATTCGCCTGATAAGAATATTTTGTTTCTGCTGCTTCTGTCCACCTTAATATTCTCCTTCTATTTGTAGATATGATAGACTCCTATTTTTCTTGTTTTATATTATGACCACACACATCTCTGCTGGAAAGTCAACATGTAGTAAGCAAGATTTAACTGTTTGATTATAACTGTGCAAATACAGAAAAAAAGAAGGCTGGCTGAAAGTTGAGTTAAACTTTGACAGTTTGATAATATTTGGTTCTTAGGGTTTTTTTTTTTTTTAGCATTCTTAATAGTTACAGTTGGGCATGATTTGTACCATCCACCCATACCCACACAGTCACAGTCACACACACATATGTATTACTTACACTATATATAACTTCCTATGCAAATATTTTACCACCAGTCAATAATACATTTTTGCCAAGACATGAAGTTTTATAAAGATCTGTATAATTGCCTGAATCACCAGCACATTCACTGACATGATATTATTTGCAGATTGACAAGTAGGAAGTGGGGAATTTTATTAAGTTACTCGTTGTCTGGGGAGGTAAATAGGTTAAAAACAGGGAAATTATAAGTGCAGAGATTAACATTTCACAAATGTTTAGTGAAACATTTGTGAAAAAAGAAGACTAAATTAAGACCTGAGCTGAAATAAAGTGAGTGGAAATGGAAATAATGGTTATATCTAAAACATGTAGAAAAAGAGTAACTGGTAGATTTTGTTAACAAATTAAAGAATAAAGTTAGACAAGCAACTGGTTGACTAATACATTAAGCGTTTGAGTCTAAGATGAAAGGAGAACACTGGTTATGTTGATAGAATGATAAAAAGGGTcgggcgcggaggctcacgcctgtaatcccagccctttgggaggccgaggtgggcagatcacgaagtcagtagtttgagaccagcctggccaacatagtgaaaccccgtctctactaaaaatacaaaaaaaaaattagctgggtgtggtggcagtcacctgtagtcccagctacttgggaggatgaggcaggagaatcgcttgaacctgggaggcggaggttgcagtgagccgagatcgcaccagtgcactccagccttggtgacaatgggagactccatctcAAAAAAAAAAAAAAAAAAAAAAAGATAAAAAGTCAGAAATCTGAAAAGTGGAGGAAGAGTACAAATAGACCTAAATTAAGCTCATTTTTAGGCTTTGATTTTGGGGAGACAAAGGGAAATGCAGCCATAGAGGGCCTGATGACATCCAATACAGAGTTCTGGTAAAGATAAAATTTGATACAGGTTTGGTGTCATTATAAGAGAAATCATTATTAAATGAAGCAAGTTAACACTCTAAGAGAATTATTTTGAGATAGAAGTGAAGCTAAGCTAAACTTCACATGCCTATAATTGGAGGGAAAAACTAAGGATAAAATCTAGCCTAGAAGATACAATAATTAGTCATAAACATGCATTGTGAAACTGTAGAGAGCAGGTAGCCCAAAATAGAGAAAGATTAGATAAAGAGAAAATAAGTATCCATCAGAGACAGTATCTCTAGGCTTGGGCAAGAGAAAAGTCCACAGTGATAAGCAACTCCACCTAAGGCATGAATATGCGGCAGAGAAAACAGCAATAGTGAATGAATGCAAAAGGTGCTGAGAAATTCCACACATGAGTATTGTGATGAGTAAATGAATAAAACATTTGCAAAGACCTTTAGAGAAAGAGAATGGGAGCATATGTGAGAAATAAGATAGTTGATTATGAATAGAAGGTAGTGAAGAAAAGCAAGCTAAGAAAAAATTCTGTTTATAAAAGAAGGAAAAGATAGTTTATGTTTTTAGCCTAAGTATAAGAGTCCTACAGATGGACTGAAAAAAATCAGTCTGAGAGTATTAGTCACAATTAATGAAATAATTACATTTTATGTATTGAGGATGCCAAGATTAAAAGGTGACAGGTAGATGTTAATTTCCCTAGATTGTGAAAGTGATCACGACAATCACACAACAAATAATTAAGTGACTTGGTATGCTTTATTTAATTGTAGGGCCTGAGGTTTTCCATTCTCATTTTTCTAAAATACAATTTTGTTTCTCCAAATTTGACAGCAGAATAAAAACCCTACCCTTTCACTGTGTATCATGCTAAGCTGCATCTCTACTCTTGATCATCTGTAGGTATTAATCACATCACTTCCATGGCATGGATGTTCACATACAGACTCTTAACCCTGGTTTACCAGGACCTCTAGGAGTGGATCCAATCTATATCTTTACAGTTGTATAGTATATGATATCTCTTTTATTTCACTCAATTTATATTTTCATCATTGACTACATATTTCTTATACACAACACACAATTTATGAATTTTTTCTCAAGATCATTCTGAGAGTTGCCCCACCCTACCTGCCTTTTATAGTATGCCCACCTCAGGCAGACACAGAGCACAATGCTGGGGTTCTCTTCACACTATCACTGCCCCAAATTGTCTTTCTAAATTTCAACTTCAATGTCATCTTCTCCATGAAGACCACTGAATGAACACCTTTTCATCCAGCCTTAATTTCTTGCTCCATAACTACTCTATCCCACGATGCAGTATTGTATCATTAATTATTAGTGTGCTTGTGACCTCCTTATGTATTCTCAATTACCTGTATTTGTGCAATAAATTGGAATAATGTAACTTGATTTCTTATCTGTGTTTGTGTTGGCATGCAAGATTTAGGTACTTATCAAAGATAATGGGGAATTAAGGCATCAATAAA >gi|28626515|ref|NM_007257.3| Homo sapiens paraneoplastic antigen MA2 (PNMA2), mRNA GGTCATTTGTCCAGAAAACTTTGTGACTGTCTTTGAGTGACCTAGTCTGGGACCCATTCATTGGTGGGTTCTAAGGTTAG AAGCTCATCCAGGATATTTTCAATATTAAGTCAGTGCATAGCTGCACCACTAACAAATTGGTGCCTGTAGAGTCAGAGTG GGTCAATTCTTAGGACAATGGCGCTGGCACTGTTAGAGGACTGGTGCAGGATAATGAGTGTGGATGAGCAGAAGTCACTG ATGGTTACGGGGATACCGGCGGACTTTGAGGAGGCTGAGATTCAGGAGGTCCTTCAGGAGACTTTAAAGTCTCTGGGCAG GTATAGACTGCTTGGCAAGATATTCCGGAAGCAGGAGAATGCCAATGCTGTCTTACTAGAGCTTCTGGAAGATACTGATG TCTCGGCCATTCCCAGTGAGGTCCAGGGAAAGGGGGGTGTCTGGAAGGTGATCTTTAAGACCCCTAATCAGGACACTGAG TTTCTTGAAAGATTGAACCTGTTTCTAGAAAAAGAGGGGCAGACGGTCTCGGGTATGTTTCGAGCCCTGGGGCAGGAGGG CGTGTCTCCAGCCACAGTGCCCTGCATCTCACCAGAATTACTGGCCCATTTGTTGGGACAGGCAATGGCACATGCGCCTC AGCCCCTGCTACCCATGAGATACCGGAAACTGCGAGTATTCTCAGGGAGTGCTGTCCCAGCCCCAGAGGAAGAGTCCTTT GAGGTCTGGTTGGAACAGGCCACGGAGATAGTCAAAGAGTGGCCAGTAACAGAGGCAGAAAAGAAAAGGTGGCTGGCGGA AAGCCTGCGGGGCCCTGCCCTGGACCTCATGCACATAGTGCAGGCAGACAACCCGTCCATCAGTGTAGAAGAGTGTTTGG AGGCCTTTAAGCAAGTGTTTGGGAGCCTAGAGAGCCGCAGGACAGCCCAGGTGAGGTATCTGAAGACCTATCAGGAGGAA GGAGAGAAGGTCTCAGCCTATGTGTTACGGCTAGAAACCCTGCTCCGGAGAGCGGTGGAGAAACGCGCCATCCCTCGGCG TATTGCGGACCAGGTCCGCCTGGAGCAGGTCATGGCTGGGGCCACTCTTAACCAGATGCTGTGGTGCCGGCTTAGGGAGC TGAAGGATCAGGGCCCGCCCCCCAGCTTCCTTGAGCTAATGAAGGTAATACGGGAAGAAGAGGAGGAAGAGGCCTCCTTT GAGAATGAGAGTATCGAAGAGCCAGAGGAACGAGATGGCTATGGCCGCTGGAATCATGAGGGAGACGACTGAAAACCACC TGGGGGCAGGACCCACAGCCAGTGGGCTAAGACCTTTAAAAAATTTTTTTCTTTAATGTATGGGACTGAAATCAAACCAT GAAAGCCAATTATTGACCTTCCTTCCTTCCTTCCTTCCCTCCCTTCCTCCTTCTCTCCTTCTCTCCTCCTCTCTCCTCTC CTCTCCTCTCTTTCCTTCCTTCCTTCCTTTTTTCTTTTTCTCTTTCTTCTTTATTTCTTGGGTCTCACTCTCATCACCCA GGCTAGAGTGCAGTGGCACAAAAATCTCGGCTCACTGCAGCCTTGACTTCCCAGGCTCAGGCTCAGGTGATCCTCACACC TTAGCCTCCCAAGTACCTGGGACTACAGGCACGCACCACCATGCCTAGCTATTCTTTTGTATTTTTGGTAGAGACAGGGT TTTGCTGTGTTGCTCAGGCTGGTCTGGAACCCCTAGGCTCAAATGATGTGCCCAACTCGGCCTCCCAAAGTGCTGGGATT ACAGGCATGAACCGCCATGCCTGGCCCTTGATTTTTCTTTTTAAGAAAAAAATATCTAGGAGTTTCTTAGACCCTATGTA GATTATTAATGAACAAAAGATTAAACTCCAAATATTAAATAGTAAGCCTGAAGGAATCTGAAACACTTGTACTTCCAATT TTCTTTAAATAATCCCAAATAGACCAGAATTGGCCCATACCATAGAAGAAAGAATTGGCAGTCAAAAAAAAAAATACCTT TTGTAATGTTTGAAAAATAAAGCTGTTTGACTTGTCAGGTGTTTTCCTTTCTCAAATCAGCAAATTCTCTCTGAGTGCCT GGCTTTGTGAGACACTGTACAAGGAGTTACAAGACTACAGCTATAACCTGCAGTTGAGCAGTTATAAACCTACAAAATGG GCCCTGCCCTCAGAGAGGTTCCAGTCTAGATGAGGAGCTGATCTAGACAGGTAAAAGGCTAACTAACCCTTTGTGTAAAT AAGTTCATCACCCCAGTAAAAGTGTCATCACCCAGTGAATAGGACCACCTCTGCCTGCAGATTTTTGTTGTTGTTGTTGT CATTGTTGTTGTTGTTTTAACCTGGGAAGTGTTCTTCCTGCCTTTCTGCTAGGTGTCAGATAGATGGTCCCAGAGCTAGG TGCTGTGTCAGGCCCTGAAGACACAGATGACTCAACCTAAGCTTTACTTTCCAGAGGTCCACAGCCTGAGAGGTGTCCCC AAAGAAAGGGGGACATGAGGGGACTGCATGCTTGAGAGCAGGGTTGTTTAGGGCAGGTTTGGATTTAGTGAGCAGGCTGG TTTGCTTAGAGAAGGCTTTTAGTGGCAACAAAGGATGAAGAGGAGAGAAAAGGAACTCACATTTATTGAGGGCCTACTGT GTGCAAAGTGTTTCATGTATATCTCATTGAATGTATACAGCCACCCTGTTGTGGTATAATTTTGCTCTTTATAAAGAGAA AGACCGAAGCTCAGATGAGTTAAGTGGTCTCCTCAACACCAAAATGCCAAGAAGTGATGGAGCCTAGACAGAAGCCCAGA ACTTTCTGACTCACACTAGTCCATCCTCTACCATCACGATGACTTTCAAATTGTGCTCTGCAGTTCTGCAGATTTTCTAG CAGTGCCATCTCCAAAATGTGTTTTAAACTCTTTATTTTTTTAATTATTATTAGTATTATTTTGAGACTGAGTCTTGCTC TATCACCCAGGCTGGAGTGCAGTGGTGCAATCTCAGCTCACTGCAACCTCTGCCTCCCAGGTTCAAGCGATTTCGTGCCT CAGCCTCCCGAGTAGCTGGGATTACAGGCACCCACCACCACGCCCAGCTAATTTTTGTATTTTTAGTAGAAATGGGGTTT CACCATGTTGGCCAGGCTGGTCTCGAACTCCTGACCTCAAGTGATCCACTCACCTCGGCCTCCCAAAGTGCTGGGATTAC AGGTGTGAGCCACCATGCCTGGGCTAAACTCTTTAAGTCTCTAGTAAATGCAGCTAGATTCAAATGGGCTGATAACCAAA TTTTAACACATCAGCATTCACCACCAGGTTTACTTTTATTTTCAGATTGGCTCATTTTGTGCAGACCTTAGAGCAAAGTT TCCTTTATGGTATCTGTGTACGTATCCAAACTTCTTTTAATTGTTCACAGATTTTAAAAGCGGTAGCACCACATGGTTGT GTAGATCAGACCTGTGTATTTAGATCAGACCTGTGTATCACGTAAGTGTGTGAGTGCAGTGCAGATGAGCACCATTTAGT TATATGTGCTAGGCAAATCTCCAACACAGTTGATGTGTAGTCTTGTGGTAGATTTGTGCATACTGTAAGCAAATTGCTTA GCTTCTCTAGACATCAGTTTCCACATCTGAAAAATAAGAAGATGAGAGTACACGGTTGTTATGAACAAATGACTTAATGC TTTTTAAGCACGTTGCATGACATCTGGAACACAGAAAGCCCTCAATACATTGAAGCTCTTAGGATTTTCACGATGTTCCT GTCTGCTCAATGCATGCTTTCTTTATTGTTCTGACAGTTGTGTGGTAACAAGCTAATATGCTTCCAGTTGACTTCCAGTC TACCCTGGTGTTAGAAACCGTTTCATCTCTTATTGTAAATTTGAGTGCTTGTTGTTTTTTATATTTGTGATGACTCTTCC AGCAGTTGTTGACAATTGTTAGAGGTTTGACTTTTAAATAATTACTTATTTTTTCTGATTGTGGTTCAGTTTAACTGAAG AATATCCTGAGATTGTAAGAAAAGCATTTTTTAAAAGGTATCACTTGTGATCATTTATCTTTCTAAATTCTATTTTTAAT ACTGTTCCACCAAAGTGATGCAGTGGTTACCATGACACCCTAATTTCATGTGTTTTTGTATTTATGAAAATAGTTTCATT GTCATTTATTGGCGGTATACAAAGTAAAATGTTATAAATGTGAAGTTATAAAATAAATATATGCTAATAAAATCCTGAGT TTTTCTGATTCCT >gi|31377729|ref|NM_020143.2| Homo sapiens putatative 28 kDa protein (LOC56902), mRNA TGGCTTCTGCGTGGTGCAGCTGCGCACGTGTTTCAGCCGGCAGCGCTTTAAGATTTCCGGGGATGGAATCCGAAATGGAA ACGCAGAGCGCCAGGGCAGAGGAGGGCTTTACCCAGGTCACCCGCAAGGGTGGCCGACGGGCGAAGAAACGACAGGCTGA ACAGCTGTCCGCAGCAGGAGAGGGCGGGGATGCGGGCCGCATGGACACAGAGGAGGCCAGGCCGGCGAAGAGGCCCGTCT TCCCACCCCTCTGTGGGGACGGGCTCCTGAGTGGGAAAGAAGAAACAAGGAAAATTCCAGTCCCAGCTAACAGATACACA CCATTGAAAGAAAACTGGATGAAGATATTTACTCCTATTGTGGAACATTTGGGACTTCAGATACGCTTTAACTTGAAATC AAGGAATGTAGAAATCAGGACTTGTAAAGAAACCAAGGATGTTAGTGCTCTGACAAAAGCAGCTGATTTTGTGAAAGCTT TTATTCTCGGCTTTCAGGTGGAGGATGCACTTGCCCTCATCAGGTTGGATGACCTCTTCCTAGAGTCTTTTGAAATTACA GATGTTAAACCCCTAAAGGGAGACCATCTATCCAGGGCAATAGGAAGAATCGCTGGCAAAGGAGGAAAAACCAAATTCAC CATAGAGAATGTGACACGGACAAGGATAGTTTTGGCTGATGTGAAAGTTCACATCCTTGGCTCCTTCCAAAATATCAAGA TGGCAAGAACTGCCATTTGCAACCTAATCTTGGGAAATCCTCCTTCCAAGGTTTATGGCAATATTCGAGCTGTGGCTAGC AGATCAGCAGATCGATTCTGATTTCAAGTCAGAGACTTTTTATCTTGCCTTTGGACTCTGGTGAAAAATACTTTACAGTG GTCGGTCACAAGAAACCAGCTGAACAATTTCAGTCATTTGAAGCCTCCGTCCCTTCTTCCATTCTCAGCCAGAAGCATAA ACAGAAAAGAAAGATTTAAGAGGATTCACACTCAACAGGTTTTAGGATAATTTAAATATCAAAAATTGATTGTTATACTT AACACATTAGGTATAATTTATCATTTATCTGAAATCACATGTAGCAGATTGCATAGTCTGTAATCCTCTCAGAGGGAAAC TTCTTGTTTAAACAGCTCTATATGGATTTATACTTTTATATTTATAAATTTATAACTTCATACAAATTTATAAACATTTC TTTATAAATTGTAATTTAATAGATTATCTCAGAAAAACCTCTCTGAATGATGACCCTTCCTTAATACTGGGTGATGTGTG AATATTTGTTTGTTGGCAGACAGGGTCTCACTTTGTCACCCAGGCTAGAGTGCAGTGGTGCAATCTCAGCTCACTGCAGC CTCTGCCTCCTGAGTTCAAGTGATCCTCCTGCTTCAGCCTCCCTAGTAGCTGGGACTACAGGTATGCACCACCATGCCTG GCTAATTTTTTGTATTTTTTGTAGAGATGGGGTTTCGCCATGTTGACCAGGCTGGTCTTGAACTCCTGGCCTCAAGGGAT CCGTCCGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGCATAAGCCACTGCGCCTGGCCTTGATGTGTGAATATTTGAGA GGTCATAAGCAGTGGTTTTGGCCATACCGTATTATACCATATACATCAGTAAGAGCTCATCTTGGAACCTGTTTTGCAGT TTCTTGCAGTTTCAAAAATTAAAGACCTACATCACAGGGTTAATGTGAAGAAAGCTTTATTTTTCAAATGAGTATTTAAT GAAAGTATACATAACCAATGTTGGGTATACAGATGCTTCTCAACTTATGATGGGTTTAGGTCCAGATAAGCCCACTGTGA GTTGAAAATACCAAAAGTCAAACATCATAGCTTAGCCTACCTTAAAAGGGCTCCGAACACTACATTAGCCTACAGTTGGG CAAAATCGTCTAATACAAAGCCTATTTTATAATAAAGTATGTTGAATATCTCATGTAAAAAAAAAAAAAAAAAA altcdfenvs/inst/exampleData/slamf_targets.RData0000644000175200017520000000765314710217111022705 0ustar00biocbuildbiocbuild흻%D/{D LGr,PW껆 "z#"vxryzo//Oo?v}﷪̮-:XOy49~]jz<:k5X=x{}ztݫ>&ZonS'^רkcBkGa2^y`բt5\XK-R3^&Xm0R_s[?֏腘.t߲Pcjˌ.kikIVCGwizxXDFrzXAHTa 6S^k[\;fZZ:/| LO8eGVkUf ])%1xGYfQbȵJj8W+JD)58X¾2j-uQq%>1fӃPc,^$#Ԇ!J)}\"^pp}8P:1Y}"+jUղTCKY' 4 `BhLoQi9Q ƑB0*$ Y4 496̀`_-m_)B+X&Zy&Ӷ2+< ,gRF5^16tʜd# Nȅ/IVb kh86k,D! ؐM 2H 4V6h $W?ʉH'Y 0J 2L ~h ^duEV6Y}^\媟G?)UޤhV 33Zd_WTA9ޛ ^##@)gc@J-]Rc Oo#3)ؓk G-Rh>iBC]*ĆmmNem OgZ{Tf,Sj"J":7MUۆbՆ,=Yg-ˑ6'!5i;EIyt|4RrMʔYGbJQHBg(ٵtmNeWI`ذɍi烸p,Q`BkdKES v]w1{ؾiq46ٸ~j2i#y54 ST*3E3)\7':laK C| 4. є?{l,~F̠o *YP2 &(HQY5lp}3O;HIQ#x{sLXgg%`T,wV?I {j_%^/z׫_/zK^F>?NOq>scQ+ aPW͓iQ$T0X~HH$& SΑr 0k0MZѵiaE*Z{ozՎ3)1ń&%5me Bdjӫe`[heCq.lQ` 'ЩD?ܧay©}`͜h󪡰4吶iLnuh-Gn$J'jB4ė8:<,՚5ҰGQ H*h"LtGK,cuHKv Ѳs}kK 4z˕BQ  k59ЗQDt!V{jLe]0R8כQ\ ],Ӭ5ZDQ̈j*0>zWx>V8a u?Hꢃ5 |]GƂٌ_¸%(ܞhm%Na.$M~S"e u9"WÑ1TFA!"bE%: eC̥ G%^_~!T#gr/E'˜2$u`-5ũzM Lt_7{Q\s/ˁjJl{t(3Rf>U͚fk)gs1*FGy{ҙߎμߥ.wK]﷭^.wK]μt3/yKg:, b&J#Nj7)c7kC0"48$$*yj;iDii8odߟ)SQ0ab݇#vV^-yCҬm%8Jck!nfl=O$/DFX(JsDf!HԫsӜe f{.:9!d|Y mBCMar9 t;\!RAiiN O½cʍ2<cdAT{aHI{m( 40ک47anQ, یmBO끟MȮ? }0ŲJ#t &&PAt^Vی2(L >VN@|X=dAާ`i9Z `ފiJQ(" <)c❘Zre8q"NwoY%r9 δGi;<1;VS#^MQ0LJ2^=aQSV3`3Ce$cۨl g͡F3̫gf*՘iځ޶O3#$^wu\!&=Ӻo@HIE*@]1Z VqU=,Ez_Fhfc/rpa¾8HĬ&(m;63YS).4%k.p6iDþw[MfL`T^dkGB,NN3%/}K~_ߗ%IDv9(($,}FlP$`>aaq*}L(42 56t:d\V+n4"s5;ʍ[ҀH 51R"euiVkǠEL {&r&} ;.%a?Kn@ոz7tfgR"܊5-(Ȯ|RT> `dL117p'_"Lل''{0N{ԅ#j'O/q,ialtcdfenvs/inst/internalData/0000755000175200017520000000000014710217111017303 5ustar00biocbuildbiocbuildaltcdfenvs/inst/internalData/chipspecs.tab0000644000175200017520000000021314710217111021750 0ustar00biocbuildbiocbuild## A tab separated file to store chip characteristics Name nrow ncol HG-U95A 640 640 HG-U95Av2 640 640 MG-U74A 640 640 MG-U74Av2 640 640 altcdfenvs/man/0000755000175200017520000000000014710217111014473 5ustar00biocbuildbiocbuildaltcdfenvs/man/AffyProbesMatch-class.Rd0000644000175200017520000000353114710217111021104 0ustar00biocbuildbiocbuild\name{AffyProbesMatch-class} \docType{class} \alias{AffyProbesMatch-class} \alias{combine,AffyProbesMatch,AffyProbesMatch-method} \alias{show,AffyProbesMatch-method} \alias{toHypergraph,AffyProbesMatch-method} \title{Class "AffyProbesMatch"} \description{ Store the results of a call to \code{matchAffyProbes}. } \section{Objects from the Class}{ Objects can be created by calls of the form \code{new("AffyProbesMatch", ...)}. An object will store the result of matching probe sequences against target sequences. } \section{Slots}{ \describe{ \item{\code{pm}:}{Object of class \code{"list"}: each element is vector of index values} \item{\code{mm}:}{Object of class \code{"list"}: each element is vector of index values} \item{\code{labels}:}{Object of class \code{"character"}} \item{\code{chip_type}:}{Object of class \code{"character"} and of length 1.} \item{\code{probes}:}{Object of class \code{"ANY"}: the \code{probetable} object used to perform the matches. } } } \section{Methods}{ \describe{ \item{combine}{\code{signature(x = "AffyProbesMatch", y = "AffyProbesMatch")}: combine two instances. This is can be useful when splitting the list of target sequences to parallelized the job.} \item{show}{\code{signature(x = "AffyProbesMatch")}:Show the instance.} \item{toHypergraph}{\code{signature(object = "AffyProbesMatch")}: build an \code{\link[hypergraph]{Hypergraph}} from the matches.} } } %\references{ ~put references to the literature/web site here ~ } %\author{ ~~who you are~~ } %\note{ ~~further notes~~ } % % ~Make other sections like Warning with \section{Warning }{....} ~ % %\seealso{ % ~~objects to See Also as \code{\link{~~fun~~}}, ~~~ % or \code{\linkS4class{CLASSNAME}} for links to other classes %} \examples{ showClass("AffyProbesMatch") } \keyword{classes} altcdfenvs/man/CdfEnvAffy-class.Rd0000644000175200017520000001172214710217111020043 0ustar00biocbuildbiocbuild\name{CdfEnvAffy-class} \docType{class} \alias{CdfEnvAffy-class} \alias{geneNames,CdfEnvAffy-method} \alias{index2xy,CdfEnvAffy-method} \alias{indexProbes,CdfEnvAffy,character-method} \alias{plot,CdfEnvAffy,missing-method} \alias{show,CdfEnvAffy-method} \alias{xy2index,CdfEnvAffy-method} \alias{coerce,CdfEnvAffy,environment-method} \alias{coerce,CdfEnvAffy,Cdf-method} \alias{toHypergraph,CdfEnvAffy-method} \alias{[,CdfEnvAffy,character,missing,missing-method} \title{Class "CdfEnvAffy"} \description{A class to hold the information necessary to handle the grouping of probes in set of probes, and to find XY coordinates of probes on a chip} \section{Objects from the Class}{ Objects can be created by calls of the form \code{new("CdfEnvAffy", ...)}. Typically, there is an instance of the class for each type of chip (e.g. Hu6800, HG-U95A, etc\ldots). } \section{Slots}{ \describe{ \item{\code{envir}:}{Object of class \code{"environment"}. It has to be thought of as a hashtable: the keys are probe set identifiers, or gene names, and the values are indexes.} \item{\code{envName}:}{Object of class \code{"character"}. A name for the environment.} \item{\code{index2xy}:}{Object of class \code{"function"}. The function used to resolve index into xy coordinates. Unless you are an advanced user, you probably want to ignore this (and rely on the default provided with the package).} \item{\code{xy2index}:}{Object of class \code{"function"}. The function used to resolve xy coordinates into index. Unless you are an advanced user, you probably want to ignore this (and rely on the default provided with the package).} \item{\code{nrow}:}{Object of class \code{"integer"}. The number of rows of probes for the chip type.} \item{\code{ncol}:}{Object of class \code{"integer"}. The number of columns of probes for the chip type.} \item{\code{probeTypes}:}{Object of class \code{"character"}. The different types of probes stored for each probe set. In the case of Affymetrix chips, the probes are typically perfect match (pm) probes or mismatch probes (mm).} \item{\code{chipType}:}{Object of class \code{"character"}. The name of the chip type the instance is associated with. This is useful when one starts to create alternative mappings of the probes on a chip (see associated vignette).} } } \section{Methods}{ \describe{ \item{[}{\code{signature(object = "CdfEnvAffy", i = "character", j = "missing", drop = "boolean")}: subset a cdf, that is return a new cdf containing only a subset of the probe sets. The subset of probe sets to take is identified as a vector of identifiers (mode "character").} \item{coerce}{\code{signature(object = "CdfEnvAffy", "environment")}: coerce an instance of the class to an \code{environment}.} \item{coerce}{\code{signature(object = "CdfEnvAffy", "Cdf")}: coerce an instance of the class to a \code{Cdf}.} \item{geneNames}{\code{signature(object="CdfEnvAffy")}: Return the names of the known probe sets (of course, it depends on the associated CDF).} \item{index2xy}{\code{signature(object = "CdfEnvAffy", i="integer")}: convert index values into XY coordinates.} \item{indexProbes}{\code{signature(object = "CdfEnvAffy", which = "character", probeSetNames = NULL)}: obtain the indexes for the probes associated wit the probe set name \code{probeSetNames}. When \code{probeSetNames} is set to \code{NULL} (default), the indexes are returned for the probe sets defined on the chip. See \code{indexProbes.CdfEnvAffy}} \item{plot}{\code{signature(x = "CdfEnvAffy", y = "missing")}: Plot the chip. It mainly sets coordinates for further plotting (see examples). See \code{plot.CdfEnvAffy}} \item{show}{\code{signature(object = "CdfEnvAffy")}: Print method.} \item{xy2index}{\code{signature(object = "CdfEnvAffy", x="integer", y="integer")}: convert XY coordinates into index values.} \item{toHypergraph}{\code{signature(object = "CdfEnvAffy")}: convert XY coordinates into index values.} } } %\references{ ~put references to the literature/web site here ~ } \author{Laurent Gautier} %\note{ ~~further notes~~ } % ~Make other sections like Warning with \section{Warning }{....} ~ \seealso{ \code{\link{indexProbes.CdfEnvAffy}}, \code{\link{plot.CdfEnvAffy}} % ~~objects to See Also as \code{\link{~~fun~~}}, ~~~ % or \code{\link{CLASSNAME-class}} for links to other classes } \examples{ ## build an instance library(hgu95acdf) cdfenv.hgu95a <- wrapCdfEnvAffy(hgu95acdf, 640, 640, "HG-U95A") show(cdfenv.hgu95a) ## find the indexes for a probe set (pm only) ip <- indexProbes(cdfenv.hgu95a, "pm", "1000_at")[[1]] ## get the XY coordinates for the probe set xy <- index2xy(cdfenv.hgu95a, ip) ## plot the chip plot(cdfenv.hgu95a) ## plot the coordinates plotLocation(xy) ## subset the environment cdfenv.hgu95a.mini <- cdfenv.hgu95a["1000_at"] } \keyword{classes} altcdfenvs/man/appendCdfEnvAffy.Rd0000644000175200017520000000236314710217111020131 0ustar00biocbuildbiocbuild\name{appendCdfEnvAffy} \alias{appendCdfEnvAffy} \title{ append probe sets to a CdfEnvAffy} \description{ append probe sets to a CdfEnvAffy } \usage{ appendCdfEnvAffy(acdfenv, id, i, nocopy = TRUE) } \arguments{ \item{acdfenv}{ instance of class \code{CdfEnvAffy}} \item{id}{ identifier for the probe set to add } \item{i}{ a \code{matrix} of indexes (see details)} \item{nocopy}{whether to make a copy of the environment or not (see details)} } \details{ The \code{matrix} \code{i} must have one column per probe type. For typical Affymetrix chip types, there are two probe types: \code{"pm"} and \code{"mm"}. \code{nocopy} set to \code{TRUE} means that the environment is added the probe set 'in-situ' (this can boost execution speed if you add a lot of probe sets). } \value{ An \code{CdfEnvAffy} is returned } \examples{ data(cdfenvEx) ## pm and mm probe set m <- matrix(1:10, ncol = 2) colnames(m) <- c("pm", "mm") appendCdfEnvAffy(cdfenvEx, "blabla", m) indexProbes(cdfenvEx, c("pm", "mm"), "blabla") ## pm only probe set m <- matrix(6:9, ncol = 1) colnames(m) <- c("pm") appendCdfEnvAffy(cdfenvEx, "blabla2", m) ## note that the unspecified "mm" were set to NA indexProbes(cdfenvEx, c("pm", "mm"), "blabla2") } \keyword{ manip } altcdfenvs/man/buildCdfEnv.biostrings.Rd0000644000175200017520000000320514710217111021331 0ustar00biocbuildbiocbuild\name{buildCdfEnv.biostrings} \alias{buildCdfEnv.biostrings} \title{ Build CDF environments} \description{ Build CDF environment from Biostrings matchPDict results } \usage{ buildCdfEnv.biostrings(apm, abatch = NULL, nrow.chip = NULL, ncol.chip = NULL, simplify = TRUE, x.colname = "x", y.colname = "y", verbose = FALSE) } %- maybe also 'usage' for other objects documented here. \arguments{ \item{apm}{ \code{AffyProbesMatch}} \item{abatch}{ \code{AffyBatch} } \item{nrow.chip}{number of rows for the chip type (see details)} \item{ncol.chip}{number of columns for the chip type (see details)} \item{simplify}{simplify the environment built (removing target names when there is no matching probe)} \item{x.colname}{ column name } \item{y.colname}{ column name} \item{verbose}{ verbose \code{TRUE}/\code{FALSE}} } \details{ % ~~ If necessary, more details than the description above ~~ Whenever an \code{abatch} is specified, \code{nrow.chip} and \code{ncol.chip} are not needed. Specifying the an \code{AffyBatch} in \code{abatch} is the easiest way to specify information about the geometry of a chip type. } \value{ An instance of class \code{CdfEnvAffy}. } %\references{ ~put references to the literature/web site here ~ } %\author{ ~~who you are~~ } %\note{ ~~further notes~~ % % ~Make other sections like Warning with \section{Warning }{....} ~ %} %\seealso{ ~~objects to See Also as \code{\link{help}}, ~~~ } %\examples{ %} % Add one or more standard keywords, see file 'KEYWORDS' in the % R documentation directory. \keyword{ manip } altcdfenvs/man/cdfenv.Rd0000644000175200017520000000265614710217111016240 0ustar00biocbuildbiocbuild\name{cdfenvs} \alias{wrapCdfEnvAffy} \alias{getCdfEnvAffy} \alias{buildCdfEnv.matchprobes} \alias{CdfEnv} \title{ functions related to cdfenvs } \description{ A set of functions to handle cdfenvs } \usage{ wrapCdfEnvAffy(cdfenv, nrow.chip, ncol.chip, chiptype, check = TRUE, verbose = FALSE) getCdfEnvAffy(abatch) buildCdfEnv.matchprobes(matches, ids, probes.pack, abatch=NULL, nrow.chip=NULL, ncol.chip=NULL, chiptype=NULL, mm=NA, simplify = TRUE, x.colname = "x", y.colname = "y", verbose=FALSE) } \arguments{ \item{abatch}{an \code{AffyBatch}} \item{cdfenv}{A cdfenv environment} \item{check}{perform consistency check or not} \item{chiptype}{A name for the chip type} \item{ids}{a vector of probe set identifiers for the matches} \item{matches}{a list as returned by the function \code{combineAffyBatch}} \item{mm}{The value to store for MMs} \item{ncol.chip}{The number of columns for the chip type} \item{nrow.chip}{The number of rows for the chip type} \item{probes.pack}{The name of the probe package} \item{simplify}{Simplify the environment created by removing the ids without any matching probe} \item{x.colname, y.colname}{see the \code{getxy.probeseq}} \item{verbose}{verbosity (\code{TRUE} or \code{FALSE})} } \value{ An instance of class \code{CdfEnvAffy}. } \examples{ ## See the main vignette } \keyword{manip} altcdfenvs/man/cdfenvEx.Rd0000644000175200017520000000107214710217111016524 0ustar00biocbuildbiocbuild\name{cdfenvEx} \alias{cdfenvEx} \docType{data} \title{ CdfEnvAffy} \description{ An example of \code{CdfEnvAffy} } \usage{data(cdfenvEx)} \format{ The format is: Formal class 'CdfEnvAffy' [package "altcdfenvs"] with 8 slots ..@ index2xy :function (object, i) ..@ xy2index :function (object, x, y) ..@ envir :length 2 ..@ envName : chr "ZG-DU33" ..@ nrow : int 100 ..@ ncol : int 100 ..@ probeTypes: chr [1:2] "pm" "mm" ..@ chipType : chr "ZG-DU33" } \examples{ data(cdfenvEx) print(cdfenvEx) } \keyword{datasets} altcdfenvs/man/copyCdfEnvAffy.Rd0000644000175200017520000000074614710217111017637 0ustar00biocbuildbiocbuild\name{copyCdfEnvAffy} \alias{copyCdfEnvAffy} \title{ make a copy of a CdfEnvAffy } \description{ make a copy of a CdfEnvAffy } \usage{ copyCdfEnvAffy(acdfenv) } \arguments{ \item{acdfenv}{ instance of class \code{CdfEnvAffy} } } \details{ Make a copy can be needed since a \code{CdfEnvAffy} contains an \code{environment} } \value{ A \code{CdfEnvAffy} } \seealso{\code{\link{CdfEnvAffy-class}}, \code{\link[Biobase]{copyEnv}}} \keyword{ manip }% at least one, from doc/KEYWORDS altcdfenvs/man/countduplicated.Rd0000644000175200017520000000167514710217111020162 0ustar00biocbuildbiocbuild\name{countduplicated} \alias{countduplicated} %- Also NEED an '\alias' for EACH other topic documented here. \title{ Count the number of times probes are used } \description{ This function counts the number of times the probes in a CdfEnvAffy are found in this object. } \usage{ countduplicated(x, incomparables = FALSE, verbose = FALSE) } %- maybe also 'usage' for other objects documented here. \arguments{ \item{x}{An instance of \code{CdfEnvAffy-class} } \item{incomparables}{ (not implemented yet, keep away) } \item{verbose}{ verbose or not } } \value{ An \code{environment} is returned. Each element in this \code{environment} has the same identifier than its corresponding probe set in the \code{CdfEnvAffy-class} and contains the number of times a probe is in use in the environment (instead of an index number in the \code{CdfEnvAffy-class}). } \author{ Laurent } \seealso{ \code{\link{CdfEnvAffy-class}}} \keyword{ manip } altcdfenvs/man/geneNames.Rd0000644000175200017520000000074514710217111016672 0ustar00biocbuildbiocbuild\name{geneNames.CdfEnvAffy} %\alias{geneNames.AltAffyBatch} \alias{geneNames.CdfEnvAffy} \title{ get the names of the known probe sets } \description{ get the names of the probe sets known to the CdfEnv } \usage{ %geneNames.AltAffyBatch(object) geneNames.CdfEnvAffy(object) } %- maybe also 'usage' for other objects documented here. \arguments{ \item{object}{ \code{CdfEnvAffy-class}} %\code{AltAffyBatch-class} or } \value{ a vector of mode \code{character} } \keyword{ manip} altcdfenvs/man/getxy.probeseq.Rd0000644000175200017520000000422614710217111017745 0ustar00biocbuildbiocbuild\name{getxy.probeseq} \alias{getxy.probeseq} %- Also NEED an '\alias' for EACH other topic documented here. \title{ A function to get the XY coordinates from a probes sequences data frame} \description{ A function to get the XY coordinates from a probes sequences \code{data.frame} } \usage{ getxy.probeseq(ppset.id = NULL, probeseq = NULL, i.row = NULL, xy.offset = NULL, x.colname = "x", y.colname = "y") } %- maybe also 'usage' for other objects documented here. \arguments{ \item{ppset.id}{ The probe sets of interest (a vector of mode \code{character}. } \item{probeseq}{ The probe sequence \code{data.frame} (see details). } \item{i.row}{ Row indexes in the \code{data.frame} (see details). } \item{xy.offset}{ Offset for the xy coordinates. if \code{NULL}, uses the default offset stored as an option for the affy package. } \item{x.colname, y.colname}{ The probe sequence packages have seen the names for the columns in their \code{data.frame}. This parameters exists to let us follow these changes.} } \details{ The \code{data.frame} passed as argument \code{probeseq} is expected to have (at least) the following columns: \code{Probe.X}, \code{Probe.Y} and \code{Probe.Set.Name}. When the argument \code{ppset.id} is not null, the probe sets } \value{ A \code{matrix} of two columns. The first column contains x coordinates, while the second column contains y coordinates. } \author{ Laurent } \section{Warning }{ The parameter \code{xy.offset.one} is here for historical reasons. This should not be touched, the option in the affy package should be modified if one wishes to modify this. This function should not be confused with the methods \code{index2xy} and similar. Here the the XY coordinate come from a \code{data.frame} that stores information about an arbitrary number probes on the chip. (See the `probe sequence' data packages on Bioconductor, and the package \code{Biostrings}). The methods \code{index2xy} are meant to interact with instances of class \code{AffyBatch}. } %\seealso{ ~~objects to See Also as \code{\link{~~fun~~}}, ~~~ } \examples{ ##---- Should be DIRECTLY executable !! ---- } \keyword{ manip } altcdfenvs/man/index2xy.Rd0000644000175200017520000000160714710217111016540 0ustar00biocbuildbiocbuild\name{index2xy} \alias{index2xy} \alias{index2xy.CdfEnvAffy} %\alias{index2xy.AltAffyBatch} \alias{xy2index} \alias{xy2index.CdfEnvAffy} %\alias{xy2index.AltAffyBatch} \title{ Functions to shuttle from indexes to XY coordinates } \description{ Functions to shuttle from indexes to XY coordinates. } \usage{ index2xy(object, ...) xy2index(object, ...) index2xy.CdfEnvAffy(object, i) %index2xy.AltAffyBatch(object, i) xy2index.CdfEnvAffy(object, x, y) %xy2index.AltAffyBatch(object, x, y) } \arguments{ \item{object}{An object of class \code{CdfEnvAffy}.} \item{i}{A vector of indexes.} \item{x, y}{Vectors of X and Y coordinates.} \item{\dots}{Optional parameters (not used).} } \value{ A vector of integers (for \code{xy2index} methods), or a matrix of two columns (for \code{index2xy} methods). } \seealso{ \code{\link{CdfEnvAffy-class}}} \examples{ ## To be done... } \keyword{ manip } altcdfenvs/man/indexProbes.CdfEnvAffy.Rd0000644000175200017520000000244214710217111021220 0ustar00biocbuildbiocbuild\name{indexProbes.CdfEnvAffy} \alias{indexProbes.CdfEnvAffy} %\alias{indexProbes.AltAffyBatch} \title{ indexes for probes } \description{ A function to get the index for probes } \usage{ indexProbes.CdfEnvAffy(object, which, probeSetNames = NULL) %indexProbes.AltAffyBatch(object, which, probeSetNames = NULL) } %- maybe also 'usage' for other objects documented here. \arguments{ \item{object}{ \code{CdfEnvAffy}}% or \code{AltAffyBatch}} \item{which}{ which kind of probe are of interest (see details). } \item{probeSetNames}{ names of the probe sets of interest. If \code{NULL}, all the probe sets are considered. } } \details{ The parameter \code{which} let one specify which category of probes are of interest. In the case of Affymetrix chips, probes can be \code{"pm"} probes or \code{"mm"} probes. It the parameter is set to \code{c("pm", "mm")}, both are returned. Should other categories be defined, they can be handled as well. % One can note that the method \code{indexProbes} defined for the % class \code{AltAffyBatch} in only a convenience % accessor function (since logically the indexes are computed from the cdfenv % information). } \value{ A \code{list} of indexes. } \seealso{\code{\link{CdfEnvAffy-class}}, \code{\link[affy]{AffyBatch-class} }} \keyword{ manip } altcdfenvs/man/matchAffyProbes.Rd0000644000175200017520000000460014710217111020037 0ustar00biocbuildbiocbuild\name{matchAffyProbes} \alias{matchAffyProbes} \alias{mmProbes} \title{ Match the probes on an Affymetrix array } \description{ Match the individual probes on an Affymetrix array to arbitrary targets. } \usage{ mmProbes(probes) matchAffyProbes(probes, targets, chip_type, matchmm = TRUE, selectMatches = function(x) which(elementNROWS(x) > 0), ...) } %- maybe also 'usage' for other objects documented here. \arguments{ \item{probes}{ a \code{probetable} object } \item{targets}{ a vector of references } \item{chip_type}{a name for the chip type.} \item{matchmm}{whether to match MM probes or not} \item{selectMatches}{a function to select matches (see Details).} \item{...}{further arguments to be passed to \code{matchPDict}.} } \details{ The matching is performed by the function \code{\link[Biostrings:matchPDict-exact]{matchPDict}}. The man page for that function will indicate what are the options it accepts. In the case where a large number targets are given, like when each target represents a possible mRNA, is it expected to have a largely sparse incidence matrix, that is a low number of probes matching every target. For that reason, only the index of matching probes are associated with each given target, with the function \code{selectMatches} giving the definition of what are matching probes. The default function just count anything matching, but the user can specify a more stringent definition if wanted. } \value{ \code{mmProbes} returns a vector of MM probe sequences. \code{matchAffyProbes} returns an instance of \code{AffyProbesMatch-class}. } \author{ Laurent Gautier } \seealso{ \code{\link[Biostrings:matchPDict-exact]{matchPDict}} for details on how the matching is performed, \code{\link{AffyProbesMatch-class}} and \code{\link{buildCdfEnv.biostrings}}} \examples{ library(hgu133aprobe) filename <- system.file("exampleData", "sample.fasta", package="altcdfenvs") fasta.seq <- readDNAStringSet(filename) targets <- as.character(fasta.seq) names(targets) <- sub("^>.+\\\\|(NM[^ \\\\|]+|Hs[^ \\\\|]+)\\\\| ? .+$", "", names(targets)) m <- matchAffyProbes(hgu133aprobe, targets, "HG-U133A") } % Add one or more standard keywords, see file 'KEYWORDS' in the % R documentation directory. \keyword{ manip } altcdfenvs/man/plot.CdfEnvAffy.Rd0000644000175200017520000000150014710217111017706 0ustar00biocbuildbiocbuild\name{plot.CdfEnvAffy} \alias{plot.CdfEnvAffy} \title{ A function to `plot' a CdfEnvAffy } \description{ A function to set the axis and plot the outline for a CdfEnvAffy } \usage{ \method{plot}{CdfEnvAffy}(x, xlab = "", ylab = "", main = x@chipType, ...) } %- maybe also 'usage' for other objects documented here. \arguments{ \item{x}{ a \code{CdfEnvAffy} } \item{xlab}{ label for the rows } \item{ylab}{ label for the columns } \item{main}{ label for the plot. The chip-type by default. } \item{\dots}{ optional parameters to be passed to the underlying function \code{plot}} } \details{ This function does not `plot' much, but sets the coordinates for further plotting (see the examples). } \author{ Laurent } \seealso{\code{\link{CdfEnvAffy-class}} } \examples{ ## See "CdfEnvAffy-class" } \keyword{ hplot } altcdfenvs/man/removeIndex.Rd0000644000175200017520000000334414710217111017253 0ustar00biocbuildbiocbuild\name{removeIndex} \alias{removeIndex} \title{ A function to remove probes in an environment } \description{ A function to remove probes in an environment, given their index. } \usage{ removeIndex(x, i, simplify = TRUE, verbose = FALSE) } %- maybe also 'usage' for other objects documented here. \arguments{ \item{x}{ An instance of \code{CdfEnvAffy-class} } \item{i}{ A vector of indexes (integers !). } \item{simplify}{ Simply the resulting \code{CdfEnvAffy} (see details). } \item{verbose}{ verbose output or not. } } \details{ The probes to be removed are set to \code{NA} in the CdfEnvAffy. When \code{simplify} is set to \code{TRUE} the probe sets are simplified whenever possible. For example, if both pm and mm for the same probe pair are set to \code{NA}, then the probe pair is removed from the probe set. } \value{ An instance of \code{CdfEnvAffy-class} is returned. } \author{ Laurent Gautier } \seealso{ \code{\link{CdfEnvAffy-class}} } \examples{ ## use plasmodiumanopheles chip as an example if (require(plasmodiumanophelescdf)) { ## wrap in a (convenient) CdfEnvAffy object planocdf <- wrapCdfEnvAffy(plasmodiumanophelescdf, 712, 712, "plasmodiumanophelescdf") print(planocdf) ## ask for the probe indexed '10759' to be removed ## (note: if one wishes to remove from X/Y coordinates, ## the function xy2index can be of help). planocdfCustom <- removeIndex(planocdf, as.integer(10759)) ## let see what happened (we made this example knowing in which ## probe set the probe indexed '10759' is found). indexProbes(planocdf, "pm", "200000_s_at") indexProbes(planocdfCustom, "pm", "200000_s_at") ## The 'second' pm probe (indexed '10579') in the probe set is now set ## to NA. } } \keyword{ manip } altcdfenvs/man/toHypergraph.Rd0000644000175200017520000000053014710217111017434 0ustar00biocbuildbiocbuild\name{toHypergraph} \alias{toHypergraph} \title{Transform to an hypergraph} \description{ Transform to an hypergraph } \usage{ toHypergraph(object, ...) } \arguments{ \item{object}{Object derived from class \code{AffyProbesMatch}.} \item{...}{Unused.} } \value{ An \code{\link[hypergraph]{Hypergraph-class}} object. } \keyword{manip} altcdfenvs/man/unique.CdfEnvAffy.Rd0000644000175200017520000000206114710217111020241 0ustar00biocbuildbiocbuild\name{unique.CdfEnvAffy} \alias{unique.CdfEnvAffy} \title{ Remove duplicated elements from a CdfEnvAffy } \description{ Remove duplicated elements from a CdfEnvAffy } \usage{ \method{unique}{CdfEnvAffy}(x, incomparables = FALSE, simplify = TRUE, verbose = FALSE, ...) } %- maybe also 'usage' for other objects documented here. \arguments{ \item{x}{ An instance of \code{CdfEnvAffy-class} } \item{incomparables}{ (not yet implemented) } \item{simplify}{ simplify the result } \item{verbose}{ verbose or not } \item{\dots}{ (here for compatibility with the generic \code{unique}) } } \details{ The parameter \code{simplify} has the same function as the one with the same name in \code{countduplicated}. } \value{ An instance of \code{CdfEnvAffy-class} in which probes used several times are removed. } \author{ Laurent } \section{Warning }{The function differs slightly from the generic \code{unique}. Here the elements found in several place a merely removed.} \seealso{\code{\link{countduplicated}} } \examples{ ##not yet here... } \keyword{ manip } altcdfenvs/man/utils.FASTA.Rd0000644000175200017520000000541714710217111016766 0ustar00biocbuildbiocbuild\name{read.FASTA.entry} \alias{read.FASTA.entry} \alias{print.FASTA} \alias{write.FASTA} \alias{skip.FASTA.entry} \alias{read.n.FASTA.entries} \alias{read.n.FASTA.headers} \alias{read.n.FASTA.sequences} \alias{read.n.FASTA.entries.split} \alias{countskip.FASTA.entries} \alias{read.FASTA.entry} \alias{grep.FASTA.entry} \title{Functions to work with FASTA files / connections} \description{ Set of function to work with biological sequences stored in FASTA format. } \usage{ countskip.FASTA.entries(con, linebreaks = 3000) grep.FASTA.entry(pattern, con, ...) \method{print}{FASTA}(x, ...) read.FASTA.entry(con, linebreaks = 3000) read.n.FASTA.entries(con, n, linebreaks = 3000) read.n.FASTA.entries.split(con, n, linebreaks = 3000) read.n.FASTA.headers(con, n, linebreaks = 3000) read.n.FASTA.sequences(con, n, linebreaks = 3000) skip.FASTA.entry(con, skip, linebreaks = 3000) write.FASTA(x, file="data.fasta", append = FALSE) } %- maybe also 'usage' for other objects documented here. \arguments{ \item{append}{append to the file (or not)} \item{con}{a \link{connection}} \item{file}{a file name} \item{linebreaks}{(to optimize the parsing, probably safe to leave it as it is)} \item{n}{number of entries to read} \item{pattern}{a pattern (to be passed to the function \code{grep})} \item{skip}{number of entries to skip} \item{x}{a FASTA sequence object} \item{...}{optional arguments to be forwarded to the function \code{print} or to the function \code{grep}} } \details{ \code{countskip.FASTA.entries} skips the remaining FASTA entries currently remaining in the connection and return the count. \code{grep.FASTA.entry} returns the next FASTA entry in the connection that matches a given regular expression. \code{print.FASTA} prints a FASTA object. \code{read.FASTA.entry} reads the next FASTA entry in the connection. \code{read.n.FASTA.entries} reads the \code{n} next FASTA entries and returns a \code{list} of FASTA objects. \code{read.n.FASTA.entries.split} reads the \code{n} next FASTA entries and returns a list of two elements: headers and sequences. \code{read.n.FASTA.headers} reads the \code{n} next FASTA headers. \code{read.n.FASTA.sequences} reads the \code{n} next FASTA sequences. \code{skip.FASTA.entry} skips a given number of FASTA entries. \code{write.FASTA} write a FASTA object into a connection. % ~~ If necessary, more details than the __description__ above ~~ } \value{ The value returned depends on the function. See above. } \author{ Laurent Gautier } \examples{ filename <- system.file("exampleData", "sample.fasta", package="altcdfenvs") con <- file(filename, open="r") fasta.seq <- grep.FASTA.entry("NM_001544\\\.2", con) close(con) print(fasta.seq) } \keyword{ manip } \keyword{ IO } \keyword{ connection } altcdfenvs/man/validAffyBatch.Rd0000644000175200017520000000142014710217111017626 0ustar00biocbuildbiocbuild\name{validAffyBatch} \alias{validAffyBatch} \alias{validCdfEnvAffy} \alias{printValidCdfEnvAffy} \title{Check validity of a CdfEnvAffy.} \description{ Tries to see if a CdfEnvAffy, or a pair of AffyBatch / CdfEnvAffy is valid. } \usage{ validAffyBatch(abatch, cdfenv) validCdfEnvAffy(cdfenv, verbose=TRUE) printValidCdfEnvAffy(x) } \arguments{ \item{abatch}{ instance of \code{\link[affy]{AffyBatch-class}} } \item{cdfenv}{ instance of \code{\link{CdfEnvAffy-class}} } \item{verbose}{ verbose or not} \item{x}{object returned by \code{validCdfEnvAffy}} } \details{ The function \code{validAffyBatch} calls in turn \code{validCdfEnvAffy}. } \seealso{ \code{\link[affy]{AffyBatch-class}}, \code{\link{CdfEnvAffy-class}} } \examples{ ## To be done... } \keyword{ manip } altcdfenvs/vignettes/0000755000175200017520000000000014710267404015742 5ustar00biocbuildbiocbuildaltcdfenvs/vignettes/altcdfenvs.Rnw0000644000175200017520000002546014710217111020560 0ustar00biocbuildbiocbuild% -*- mode: noweb; noweb-default-code-mode: R-mode; -*- %\VignetteIndexEntry{altcdfenvs} %\VignetteKeywords{Preprocessing, Affymetrix} %\VignetteDepends{altcdfenvs} %\VignettePackage{altcdfenvs} \documentclass[12pt]{article} %\usepackage{amsmath} %\usepackage{hyperref} \usepackage[authoryear,round]{natbib} \textwidth=6.2in \textheight=8.5in %\parskip=.3cm \oddsidemargin=.1in \evensidemargin=.1in \headheight=-.3in \newcommand{\scscst}{\scriptscriptstyle} \newcommand{\scst}{\scriptstyle} \newcommand{\Rfunction}[1]{{\texttt{#1}}} \newcommand{\Robject}[1]{{\texttt{#1}}} \newcommand{\Rclass}[1]{{\texttt{#1}}} \newcommand{\Rpackage}[1]{{\textit{#1}}} \author{Laurent Gautier} \title{Alternative CDF environments} \begin{document} \maketitle \tableofcontents \section{Introduction} On short oligonuleotide arrays, several probes are designed to match a target transcript, and probes matching the same target transcript can be grouped in a probe set. Between the time the probes for a given short oligonucleotide chip were designed, and the time an analysis is made, the knowledge of expected transcripts for a given organism might have changed. Unless one includes the latest development in transcripts into an analysis, the analysis could suffer from what we like to call a {\it Dorian Gray}\footnote{From the novel `The Picture of Dorian Gray' by Oscar Wilde.} effect. The chip itself does not change, which means that the probes and their respective sequences remain the same, while the knowledge of the transcripts, and eventually their sequence, might evolve, and in time the immobility of the probe and probe sets give an uglier picture of the biological phenomena to study. Being able to easily modify or replace the grouping of probes in probe sets gives the opportunity to minimize this effect. The package is directly usable with {\it Affymetrix} {\it GeneChip} short oligonucleotide arrays, and can be adapted or extended to other platforms. The bibliographic reference associated with the package is given by the command: \begin{Scode} citation(package="altcdfenvs") \end{Scode} \begin{quote} Alternative mapping of probes to genes for Affymetrix chips Laurent Gautier, Morten Mooller, Lennart Friis-Hansen, Steen Knudsen BMC Bioinformatics 2004, 5:111 \end{quote} If you use it, consider citing it, and if you cite it consider citing as well other packages it depends on. To start we will first load the package: <<>>= library(altcdfenvs) @ \section{The class \Rclass{CdfEnvAffy}} Each instance of this class contains a way to group probes in probe sets. Different instances, describing different ways to group probes in probe sets, can co-exist for a given chip type. When experimenting, it is highly recommended to use the functions \Rfunction{validCdfEnvAffy} and \Rfunction{validAffyBatch} to make sure that a given instance is a valid one. \section{Reading sequence information in FASTA connections} The package contains simple functions to read {\bf R} connections in the FASTA format. Typically, collections of sequences are stored in FASTA files, which can be significantly large, one can wish to read and process sequences one after the other. This can be done by opening the file in `r' mode: <<>>= fasta.filename <- system.file("exampleData", "sample.fasta", package="altcdfenvs") con <- file(fasta.filename, open="r") @ Reading the sequences one after another, and printing information about them in turn goes like: <<>>= fasta.seq <- read.FASTA.entry(con) while(! is.null(fasta.seq$header)) { print(fasta.seq) fasta.seq <- read.FASTA.entry(con) } close(con) @ One can foresee that the matching of a set of reference sequences against all the probes can be parallelized easily: the reference sequences can simply be distributed across different processors/machines. When working with all the reference sequences in a single large FASTA file, the option \Robject{skip} can let one implement a poor man's parallel sequence matching very easily. \section{Creating an alternative mapping from sequences in a FASTA file} \subsection{Select the constituting elements} \begin{itemize} \item Chip type: For this tutorial we decide to work with the Affymetrix chip HG-U133A. \item Target sequences: The set of target sequences we use for this tutorial is in the exemplar FASTA file: <<>>= ## first, count the number of FASTA entries in our file con <- file(fasta.filename, open="r") n <- countskip.FASTA.entries(con) close(con) ## read all the entries con <- file(fasta.filename, open="r") my.entries <- read.n.FASTA.entries.split(con, n) close(con) @ \end{itemize} \subsection*{matching the probes} The package \Rpackage{Biostrings} and the probe data package for HG-U133A are required to perform the matching. The first step is to load them: <<>>= library(hgu133aprobe) @ The matching is done simply (one can refer to the documentation for the package \Rpackage{Biostrings} for further details): <<>>= targets <- my.entries$sequences names(targets) <- sub(">.+\\|(Hs\\#|NM_)([^[:blank:]\\|]+).+", "\\1\\2", my.entries$headers) m <- matchAffyProbes(hgu133aprobe, targets, "HG-U133A") @ \subsection{analyzing the matches} When the position of the match between probes and target sequences does not matter, the association can be represented as a bipartite graph. The method \Rfunction{toHypergraph} will transform an instance of \Rclass{AffyProbesMatch} into an \Rclass{Hypergraph}. <<>>= hg <- toHypergraph(m) @ Currently, there are not many functions implemented around hypergraphs, so we convert it to a more common graph. <<>>= gn <- toGraphNEL(hg) @ Since this is now a regular graph, all of probes and targets are regular nodes on that graph. Node name-based rules can be applied to identify whether a node is a target sequence or a probe. <<>>= targetNodes <- new.env(hash=TRUE, parent=emptyenv()) for (i in seq(along=targets)) { targetNodes[[names(targets)[i]]] <- i } @ Since the graph is relatively small, we can plot it, and see that one probe is common to both probe sets: <>= library(Rgraphviz) tShapes <- rep("ellipse", length=length(targets)) names(tShapes) <- names(targets) tColors <- rep("ivory", length=length(targets)) names(tColors) <- names(targets) nAttrs <- list(shape = tShapes, fillcolor = tColors) gAttrs <- list(node = list(shape = "rectangle", fixedsize = FALSE)) plot(gn, "neato", nodeAttrs = nAttrs, attrs = gAttrs) @ Whenever a large number oftarget sequences are involved, counting the degrees will be more efficient than plotting. The package contains a function to create a \Rclass{CdfEnv} from the matches: <>= alt.cdf <- buildCdfEnv.biostrings(m, nrow.chip = 712, ncol.chip = 712) @ Note that the size for chip must be specified. This is currently a problem with cdfenvs as they are created by the package \Rpackage{makecdfenv}. The class \Rclass{CdfEnv} suggests a way to solve this (hopefully this will be integrated in \Rpackage{makecdfenv} in the near future). When this happens, the section below will be replaced by something more intuitive. But in the meanwhile, here is the current way to use our shiny brand new class \Rclass{CdfEnv}: \begin{Scode} ## say we have an AffyBatch of HG-U133A chips called 'abatch' ## summary checks to avoid silly mistakes validAffyBatch(abatch, alt.cdf) ## it is ok, so we proceed... ## get the environment out of it class alt.cdfenv <- alt.cdf@envir abatch@cdfName <- "alt.cdfenv" \end{Scode} From now on, the object \Robject{abatch} will use our `alternative mapping' rather than the one provided by the manufacturer of the chip: \begin{Scode} print(abatch) \end{Scode} %\section*{Creating an alternative environment to store only perfect matches} \section{Always up-to-date} Even if alternative mapping is not used upstream of the analysis, it can still be interesting to verify probesets highlighted during data analysis. The \Rpackage{biomaRt} package makes withdrawing up-to-date sequences very easy, and those sequences can be matched against the probes. First, we create a \emph{mart}: \begin{Scode} library(biomaRt) mart <- useMart("ensembl",dataset="hsapiens_gene_ensembl") \end{Scode} (refer to the documentation for the \Rpackage{biomaRt} for further information). \subsection{Casual checking of genes} In this example, we assume that for one reason or an other a researcher would like to know more about the probes matching the SLAMF genes. <>= geneSymbols <- c("SLAMF1", "SLAMF3", "SLAMF6", "SLAMF7", "SLAMF8", "SLAMF9") @ The vector \Robject{geneSymbols} defined can easily be replaced by your favorite genes; the example below should still work. We then write a convenience function \Robject{getSeq} to extract the sequences. This function appenda a \verb+-+ to the HUGO symbol (as there might be several sequences matching). <>= getSeq <- function(name) { seq <- getSequence(id=name, type="hgnc_symbol", seqType="cdna", mart = mart) targets <- seq$cdna if (is.null(targets)) return(character(0)) names(targets) <- paste(seq$hgnc_symbol, 1:nrow(seq), sep="-") return(targets) } @ % load saved data (instead of connecting to the mart) <>= load(system.file("exampleData", "slamf_targets.RData", package="altcdfenvs")) @ The function let us obtain the target sequences very easily: \begin{Scode} targets <- unlist(lapply(geneSymbols, getSeq)) \end{Scode} The targets are matched as seen previously: <<>>= m <- matchAffyProbes(hgu133aprobe, targets, "HG-U133A") @ A colorful graph can be made in order to visualize how matching probes are distributed: <>= hg <- toHypergraph(m) gn <- toGraphNEL(hg) library(RColorBrewer) col <- brewer.pal(length(geneSymbols)+1, "Set1") tColors <- rep(col[length(col)], length=numNodes(gn)) names(tColors) <- nodes(gn) for (col_i in 1:(length(col)-1)) { node_i <- grep(paste("^", geneSymbols[col_i], "-", sep=""), names(tColors)) tColors[node_i] <- col[col_i] } nAttrs <- list(fillcolor = tColors) plot(gn, "twopi", nodeAttrs=nAttrs) @ \begin{itemize} \item Watch for \emph{SLAMF6} and \emph{SLAMF7} \item The second sequence in SLAMF8 can potentially has specific probes (the rest of the probes are matching both SLAMF8 sequences) \end{itemize} Comparison with the official mapping can be made (not so simply, a future version should address this) <<>>= library("hgu133a.db") affyTab <- toTable(hgu133aSYMBOL) slamf_i <- grep("^SLAMF", affyTab$symbol) pset_id <- affyTab$probe_id[slamf_i] library("hgu133acdf") countProbes <- lapply(pset_id, function(x) nrow(hgu133acdf[[x]])) names(countProbes) <- affyTab$symbol[slamf_i] countProbes @ The results do not appear in complete agreement with the matching just performed. \end{document} altcdfenvs/vignettes/modify.Rnw0000644000175200017520000000516014710217111017711 0ustar00biocbuildbiocbuild% -*- mode: noweb; noweb-default-code-mode: R-mode; -*- %\VignetteIndexEntry{Modifying existing CDF environments to make alternative CDF environments} %\VignetteKeywords{Preprocessing, Affymetrix} %\VignetteDepends{altcdfenvs} %\VignettePackage{altcdfenvs} %documentclass[12pt, a4paper]{article} \documentclass[12pt]{article} \usepackage{amsmath} \usepackage{hyperref} \usepackage[authoryear,round]{natbib} \textwidth=6.2in \textheight=8.5in %\parskip=.3cm \oddsidemargin=.1in \evensidemargin=.1in \headheight=-.3in \newcommand{\scscst}{\scriptscriptstyle} \newcommand{\scst}{\scriptstyle} \newcommand{\Rfunction}[1]{{\texttt{#1}}} \newcommand{\Robject}[1]{{\texttt{#1}}} \newcommand{\Rclass}[1]{{\texttt{#1}}} \newcommand{\Rpackage}[1]{{\textit{#1}}} \author{Laurent Gautier} \title{Modifying existing CDF environments to make alternative CDF environments} \begin{document} \maketitle \section*{Introduction} First we need to load the package: <<>>= library(altcdfenvs) @ The {\it Plasmodium} / {\it Anopheles} is taken as an example: <<>>= library(plasmodiumanophelescdf) @ One will adapt easily the code below for other chips. \section*{How to build a CdfEnvAffy object from the cdfenv package} The first step is to wrap the naked enviroment in the package \Rpackage{plasmodiumanophelescdf} in an object: <<>>= planocdf <- wrapCdfEnvAffy(plasmodiumanophelescdf, 712, 712, "plasmodiumanophelescdf") print(planocdf) @ The numbers $712$ and $712$ correspond to the dimension of the array. If you do not know these numbers for your chip, the easiest (for the moment) is to read CEL data in an \Rclass{AffyBatch} and call the function \Rfunction{print} on this object. Hopefully, the cdf packages offered on the bioconductor website will be modified, which will make this step (and the complication to know the dimension of the chip) unncessary. \section*{How to subset an environment using probe set ids} (see the vignette `n-genomes chips') \section*{How to work with given index / XY coordinates} \subsection*{Getting index} The method \Rfunction{indexProbes} is implemeted for objects of class \Rclass{AltCdfEnvs} <<>>= #indexProbes(planocdf, "pm", "") @ One can directly work on the CDF data, without having to load CEL data. \subsection*{Removing probe sets} The function \Rfunction{removeIndex} let one remove probe sets given their index. \subsection*{Multiple use of index} When crafting an AltCdfEnv, it can happen that probe indexes are used by several probe sets. The \Rfunction{unique.CdfEnvAffy} is designed to help one to deal with the issue. \section*{How to use this environment} (see the vignette `n-genomes chips') \end{document} altcdfenvs/vignettes/ngenomeschips.Rnw0000644000175200017520000000654214710217111021271 0ustar00biocbuildbiocbuild% -*- mode: noweb; noweb-default-code-mode: R-mode; -*- %\VignetteIndexEntry{Alternative CDF environments for 2(or more)-genomes chips} %\VignetteKeywords{Preprocessing, Affymetrix} %\VignetteDepends{altcdfenvs} %\VignettePackage{altcdfenvs} %documentclass[12pt, a4paper]{article} \documentclass[12pt]{article} \usepackage{amsmath} \usepackage{hyperref} \usepackage[authoryear,round]{natbib} \textwidth=6.2in \textheight=8.5in %\parskip=.3cm \oddsidemargin=.1in \evensidemargin=.1in \headheight=-.3in \newcommand{\scscst}{\scriptscriptstyle} \newcommand{\scst}{\scriptstyle} \newcommand{\Rfunction}[1]{{\texttt{#1}}} \newcommand{\Robject}[1]{{\texttt{#1}}} \newcommand{\Rclass}[1]{{\texttt{#1}}} \newcommand{\Rpackage}[1]{{\textit{#1}}} \author{Laurent Gautier} \title{Alternative CDF environments for 2(or more)-genomes chips} \begin{document} \maketitle \section*{Introduction} Let's start by loading the package: <<>>= library(altcdfenvs) @ The {\it Plasmodium} / {\it Anopheles} is taken as an example: <<>>= library(plasmodiumanophelescdf) @ One will adapt easily the code below for other chips. \section*{How to build a CdfEnvAffy object from the cdfenv package} The first step is to wrap the naked enviroment in the package \Rpackage{plasmodiumanophelescdf} in an object: <<>>= planocdf <- wrapCdfEnvAffy(plasmodiumanophelescdf, 712, 712, "plasmodiumanophelescdf") print(planocdf) @ The numbers $712$ and $712$ correspond to the dimension of the array. If you do not know these numbers for your chip, the easiest (for the moment) is to read CEL data in an \Rclass{AffyBatch} and call the function \Rfunction{print} on this object. \section*{How to create a CdfEnvAffy that is a subset of the 2-genomes one} If the identifiers starting with `Pf' correspond to plasmodium, it is an easy job to find them: <<>>= ids <- geneNames(planocdf) ids.pf <- ids[grep("^Pf", ids)] @ Subsetting the \Rclass{CdfEnvAffy} is also an easy task: <<>>= ## subset the object to only keep probe sets of interest plcdf <- planocdf[ids.pf] print(plcdf) @ However, this is not that simple:{\bf the environment created does not contain all the probe set ids from Plasmodium}. Unfortunately, one cannot rely on pattern matching on the probe set id to find all the probe set ids associated with Plasmodium. The list of plasmodium ids included in the package can let us build a Plasmodium-only CdfEnvAffy (contributed by Zhining Wang). <<>>= filename <- system.file("exampleData", "Plasmodium-Probeset-IDs.txt", package="altcdfenvs") ids.pf <- scan(file = filename, what = "") plcdf <- planocdf[ids.pf] print(plcdf) @ Before we eventually save our environment, we may want to give it an explicit name: <<>>= plcdf@envName <- "Plasmodium ids only" print(plcdf) @ \section*{Assign the new Cdf data to an AffyBatch} Handling of AffyCdfEnv directly in within an AffyBatch, or AffyBatch-like, structure is being completed\ldots in the meanwhile, the current mecanism for cdfenvs has to be used. If your CEL files were read into an AffyBatch named \Robject{abatch}. \begin{Scode} envplcdf <- as(plcdf, "environment") abatch@cdfName <- "plcdf" \end{Scode} From now on, \Robject{abatch} will only consider Cdf information from \Robject{plcdf}. If you want to save this further use, I would recommend to do: \begin{Scode} save(abatch, plcdf, envplcdf, file="where/to/save.rda") \end{Scode} \end{document}