Found 5896 results in 1726 files, showing top 50 files (show more).
Basic4Cseq:R/createVirtualFragmentLibrary.r: [ ] |
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49: .createVirtualFragmentLibrary_DNAString <- function(chosenGenome, firstCutter, secondCutter, readLength, onlyNonBlind = TRUE, useOnlyIndex ...(154 bytes skipped)...
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78: .splitChromosome_DNAString <- function(firstCutter, secondCutter, chromosomeToSplit, chromosomeName) {
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213: signature=signature(chosenGenome="DNAString", firstCutter="character", secondCutter="character", readLength="numeric"),
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214: .createVirtualFragmentLibrary_DNAString)
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217: signature=signature(firstCutter="character", secondCutter="character", chromosomeToSplit="DNAString", chromosomeName="character"),
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218: .splitChromosome_DNAString)
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15: if (class(chromosomeToSplit) == "MaskedDNAString") {
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bcSeq:R/bcSeq.R: [ ] |
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84: .bcSeq_hamming_DNAString <- function(sampleFile, libFile, outFile,
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120: .bcSeq_edit_DNAString <- function(sampleFile, libFile, outFile,
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105: res <- invisible(.Call("_bcSeq_CRISPR_matching_DNAString",
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145: res <- invisible(.Call("_bcSeq_CRISPR_user_matching_DNAString",
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151: res <- invisible(.Call("_bcSeq_CRISPR_matching_DNAString",
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176: .bcSeq_hamming_DNAString(sampleFile = sampleFile, libFile = libFile,
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192: .bcSeq_edit_DNAString(sampleFile, libFile, outFile,
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ShortRead:R/methods-Misc.R: [ ] |
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111: .srdistance_DNAStringSet_DNAString <- function(pattern, subject, ...)
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98: .srdistance_DNAStringSet_character <- function(pattern, subject, ...)
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121: .srdistance_DNAStringSet_DNAStringSet <- function(pattern, subject,
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100: strings <- lapply(subject, DNAString)
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118: setMethod(srdistance, c("DNAStringSet", "DNAString"),
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119: .srdistance_DNAStringSet_DNAString)
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7: setMethod(clean, "DNAStringSet", function(object, ...) {
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11: setMethod(dustyScore, "DNAStringSet",
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19: triplets <- DNAStringSet(mkAllStrings(c("A", "C", "G", "T"), 3))
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62: setMethod(writeFasta, "DNAStringSet",
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108: setMethod(srdistance, c("DNAStringSet", "character"),
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109: .srdistance_DNAStringSet_character)
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127: setMethod(srdistance, c("DNAStringSet", "DNAStringSet"),
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128: .srdistance_DNAStringSet_DNAStringSet)
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periodicDNA:R/periodicity.R: [ ] |
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293: getPeriodicity.DNAString <- function(
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109: getPeriodicity.DNAStringSet <- function(
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9: #' @param x a DNAString, DNAStringSet or GRanges object.
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291: #' @describeIn getPeriodicity S3 method for DNAString
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26: #' @param genome genome ID, BSgenome or DNAStringSet object
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107: #' @describeIn getPeriodicity S3 method for DNAStringSet
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299: seq <- Biostrings::DNAStringSet(x)
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Basic4Cseq:R/simulateDigestion.r: [ ] |
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38: .simulateDigestionChromosome_DNAString <- function(firstCutter, secondCutter, dnaSequence) {
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28: .simulateDigestionChromosome_MaskedDNAString <- function(firstCutter, secondCutter, dnaSequence) {
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68: signature=signature(firstCutter="character", secondCutter="character", dnaSequence="DNAString"),
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69: .simulateDigestionChromosome_DNAString)
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64: signature=signature(firstCutter="character", secondCutter="character", dnaSequence="MaskedDNAString"),
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65: .simulateDigestionChromosome_MaskedDNAString)
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bcSeq:src/CRISPR_matching.cpp: [ ] |
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365: SEXP CRISPR_matching_DNAString(
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472: SEXP CRISPR_user_matching_DNAString(
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triplex:src/search_interface.c: [ ] |
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352: seq_t decode_DNAString(SEXP dnaobject, int seq_type)
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346: * Decode DNAString object
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348: * @param dnaobject DNAString object
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511: * @param dnaobject DNAString object
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556: seq_t dna = decode_DNAString(dnaobject, st[0]);
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rtracklayer:src/twoBit.c: [ ] |
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9: SEXP DNAString_to_twoBit(SEXP r_dna, SEXP r_mask, SEXP r_seqname) {
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99: PROTECT(r_ans = alloc_XRawList("DNAStringSet", "DNAString", r_ans_width));
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crisprScore:R/getCasRxRFScores.R: [ ] |
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189: .extractSpacersFromDNAString <- function(dnaString,
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6: #' @param mrnaSequence A \code{DNAStringSet} represeting the mRNA sequence
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62: if (!is(mrnaSequence, "DNAStringSet")){
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63: stop("mrnaSequence must be a DNAStringSet")
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104: #' @importFrom Biostrings DNAStringSet
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113: spacers <- .extractSpacersFromDNAString(mrnaSequence[[1]],
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121: spacerSet <- DNAStringSet(spacers)
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139: protospacer <- reverseComplement(DNAStringSet(spacers$spacer))
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457: GuideSeq = DNAStringSet(dat[["spacer"]])
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752: #' @importFrom Biostrings DNAStringSet
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754: G <- DNAStringSet(x[["spacer"]])
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48: #' mrnaSequence <- Biostrings::readDNAStringSet(filepath=fasta,
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96: #mrnaSequence <- Biostrings::readDNAStringSet(filepath=fasta,
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GeneRegionScan:R/creationFunctions.R: [ ] |
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1682: DNAStringSet<-read.DNAStringSet(path)
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146: probe <- DNAStringSet(as.character(sequences)) #need to remove names or PDict will crash
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148: probe_directions <- DNAStringSet()
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1684: for(i in 1:length(DNAStringSet)){
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1687: readFASTAformatList[[i]][["desc"]]<- names(as.character(DNAStringSet))[i]
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1688: readFASTAformatList[[i]][["seq"]]<- as.character(as.character(DNAStringSet)[i])
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motifcounter:R/simulate_wrapper.R: [ ] |
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24: generateDNAString = function(len, bg) {
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68: generateDNAStringSet = function(seqlen, bg) {
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1: #' Generate DNAString
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3: #' This function generates a random DNAString of a given length
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9: #' @return A DNAString object
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29: return(Biostrings::DNAString(""))
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40: return(Biostrings::DNAString(ret[[1]]))
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21: #' motifcounter:::generateDNAString(1000, bg)
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43: #' Generate DNAStringSet
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45: #' This function generates a DNAStringSet-object of the
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53: #' @return A DNAStringSet object
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73: seqs = c(seqs, generateDNAString(seqlen[i], bg))
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76: return(Biostrings::DNAStringSet(seqs))
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197: seq = generateDNAString(seqlen, bg)
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15: #' seqs = Biostrings::readDNAStringSet(seqfile)
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23: #' @seealso \code{\link{generateDNAStringSet}}
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59: #' seqs = Biostrings::readDNAStringSet(seqfile)
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65: #' motifcounter:::generateDNAStringSet(10:50, bg)
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67: #' @seealso \code{\link{generateDNAStringSet}}
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100: #' seqs = Biostrings::readDNAStringSet(seqfile)
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132: seqs = generateDNAStringSet(seqlen, bg)
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167: #' seqs = Biostrings::readDNAStringSet(seqfile)
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248: #' seqs = Biostrings::readDNAStringSet(seqfile)
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273: seqs = generateDNAStringSet(rep(seqlen, nsim), bg)
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PWMEnrich:R/misc.R: [ ] |
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28: DNAStringSetToList = function(x){
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22: #' Convert DNAStringSet to list of DNAString objects
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39: #' @param sequences either a list of DNAString objects, or a DNAStringSet
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24: #' as.list doesn't seem to always work for DNAStringSets, so
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27: #' @param x an object of class DNAStringSet
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periodicDNA:R/utils.R: [ ] |
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58: DNAStringSet2GRanges <- function(seqs) {
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27: if (is(dna, 'DNAString')) {
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39: Biostrings::DNAString( paste(shuffled_charvec, collapse="") )
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51: Biostrings::DNAString( as.character(seq) )
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28: dna <- Biostrings::DNAStringSet(dna)
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31: dna <- Biostrings::DNAStringSet(dna)
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35: shuffled <- Biostrings::DNAStringSet(
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48: shuffled <- Biostrings::DNAStringSet(
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h5vc:R/helpers.R: [ ] |
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14: encodeDNAString <- function( ds ){
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Biostrings:src/translate.c: [ ] |
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131: SEXP DNAStringSet_translate(SEXP x, SEXP skip_code, SEXP dna_codes,
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148: "DNAStringSet_translate(): length of 'lkup' "
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152: "DNAStringSet_translate(): 'lkup' and 'init_lkup' "
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167: "DNAStringSet_translate(): "
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176: "DNAStringSet_translate(): "
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MatrixRider:inst/unitTests/test_getSeqOccupancy.R: [ ] |
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257: test_getSeqOccupancy_badDNAString <- function() {
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12: sequence <- DNAString("CACGTG")
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34: sequence <- DNAString("CACGTG")
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55: sequence <- DNAString("CACGTGCTGAAATGTCATGCATGCTAGCGTTTTGCCATGTCGATCTGACTCGTAGTGCTGTCGTTTGCGGATCGTTCGAGCTGCTGCGTATCGTGC")...(0 bytes skipped)...
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247: sequence <- DNAString("CACGTG")
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268: sequence <- DNAString("CACSTG")
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rtracklayer:R/twobit.R: [ ] |
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91: .DNAString_to_twoBit <- function(object, seqname) {
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74: invisible(.TwoBits_export(mapply(.DNAString_to_twoBit, object,
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94: if (!is(object, "DNAString") && !is(object, "MaskedDNAString"))
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95: stop("'object' must be a DNAString")
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101: .Call(DNAString_to_twoBit, as.character(object), object_mask, seqname)
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53: object <- as(object, "DNAStringSet")
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57: setMethod("export", c("DNAStringSet", "TwoBitFile"),
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TreeSummarizedExperiment:R/internal_utils.R: [ ] |
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221: .all_have_DNAStringSet <- function(args){
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230: .all_have_DNAStringSetList <- function(args){
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219: #' test all TSEs have DNAStringSet in the referenceSeq slot
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223: is(x@referenceSeq, "DNAStringSet")
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228: #' test all TSEs have DNAStringSetList in the referenceSeq slot
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232: is(x@referenceSeq, "DNAStringSetList")
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247: isDNA <- .all_have_DNAStringSet(args)
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248: isDNAList <- .all_have_DNAStringSetList(args)
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251: # 1) all TSEs have DNAStringSet
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252: # 2) all TSEs have DNAStringSetList
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258: "NULL/DNAStringSet/DNAStringSetList ")
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crisprDesign:R/findSpacers.R: [ ] |
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209: .GRanges2DNAStringSet <- function(x,
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318: .string2DNAStringSet <- function(x,
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173: .asDNAStringSet <- function(x,
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346: .findSpacersFromDNAStringSet <- function(dna,
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5: #' \linkS4class{DNAString} or character vector of genomic sequences.
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8: #' \linkS4class{DNAString} object, or a character vector of genomic
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189: } else if (methods::is(x, "DNAString") ||
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4: #' sequence(s) contained in either a \linkS4class{DNAStringSet},
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7: #' @param x Either a \linkS4class{GRanges}, a \linkS4class{DNAStringSet}, or a
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171: # Extract a DNAStringSet object from a (bsgenome,granges) pair
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185: x <- .GRanges2DNAStringSet(x,
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190: methods::is(x, "DNAStringSet") ||
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192: x <- .string2DNAStringSet(x,
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314: # Convenience function to transform a string into a DNAStringSet
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315: #' @importFrom Biostrings DNAStringSet reverseComplement
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321: dna <- Biostrings::DNAStringSet(x)
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340: # Find spacer sequences from a DNAStringSet object
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103: dna <- .asDNAStringSet(x,
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107: gs <- .findSpacersFromDNAStringSet(dna=dna,
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203: # Helper function for .asDNAStringSet
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Rsamtools:src/io_sam.c: [ ] |
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66: static SEXP _tmpl_DNAStringSet()
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69: SEXP lkup = PROTECT(_get_lkup("DNAString"));
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70: SEXP ans = new_XRawList_from_CharAEAE("DNAStringSet", "DNAString",
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112: SET_VECTOR_ELT(tmpl, SEQ_IDX, _tmpl_DNAStringSet());
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memes:R/input_methods.R: [ ] |
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11: sequence_input.DNAStringSet <- function(input){
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BSgenome:R/BSgenomeViews-class.R: [ ] |
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212: .from_BSgenomeViews_to_DNAStringSet <- function(from)
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29: elementType="DNAString"
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168: dna="DNAStringSet"
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215: setAs("BSgenomeViews", "DNAStringSet", .from_BSgenomeViews_to_DNAStringSet)
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216: setAs("BSgenomeViews", "XStringSet", .from_BSgenomeViews_to_DNAStringSet)
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272: ### DNAStringSet methods
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286: ### exact same formal args than in the method for DNAStringSet objects. This
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422: ### TODO: Add more DNAStringSet methods...
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R453Plus1Toolbox:R/alignShortReads.R: [ ] |
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1: .alignShortReads_DNAStringSet <- function(object, bsGenome, seqNames, ensemblNotation) {
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75: signature=signature(object="DNAStringSet", bsGenome="BSgenome",
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77: .alignShortReads_DNAStringSet)
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85: signature=signature(object="DNAStringSet", bsGenome="BSgenome",
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88: return(.alignShortReads_DNAStringSet(object, bsGenome, seqNames, FALSE))
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99: signature=signature(object="DNAStringSet", bsGenome="BSgenome",
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102: return(.alignShortReads_DNAStringSet(object, bsGenome, names(bsGenome)[1:24], ensemblNotation))
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113: signature=signature(object="DNAStringSet", bsGenome="BSgenome",
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116: return(.alignShortReads_DNAStringSet(object, bsGenome, names(bsGenome)[1:24], FALSE))
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141: # gSeqs = DNAStringSet(geneSeqs$gene_exon_intron)
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VariantFiltering:src/methods-WeightMatrix.c: [ ] |
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124: scoss_wm_score_DNAStringSet(SEXP wmR, SEXP dnaStringSet, SEXP nscoR) {
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122: /* entry point to wm_score_DNAStringSet */
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VariantAnnotation:src/dna_hash.c: [ ] |
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65: SEXP dna_hash_as_DNAStringSet(struct dna_hash_t *dna)
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117: "DNAStringSet", "DNAString", tag, ranges));
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3: /* DNAStringSet -- hash */
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115: /* DNAStringSet */
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triplex:R/triplex.align.R: [ ] |
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53: alignment.DNAStringSet <- function(alignment, type)
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51: ## Convert triplex alignment into DNAStringSet
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65: a <- DNAStringSet(c(
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78: a <- DNAStringSet(c(
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91: a <- DNAStringSet(c(
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104: a <- DNAStringSet(c(
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117: a <- DNAStringSet(c(
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130: a <- DNAStringSet(c(
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143: a <- DNAStringSet(c(
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156: a <- DNAStringSet(c(
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178: alignment.DNAStringSet(alignment, type)
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Biostrings:R/seqinfo-methods.R: [ ] |
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11: .get_DNAStringSet_seqinfo <- function(x)
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8: ### seqinfo() getter and setter for DNAStringSet objects
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30: setMethod("seqinfo", "DNAStringSet", .get_DNAStringSet_seqinfo)
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32: ### We implement a restricted seqinfo() setter for DNAStringSet object 'x'
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39: ### is all we need to make the seqlevelsStyle() setter work on a DNAStringSet
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58: .set_DNAStringSet_seqinfo <-
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91: setReplaceMethod("seqinfo", "DNAStringSet", .set_DNAStringSet_seqinfo)
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ShortRead:inst/unitTests/test_ShortReadQ.R: [ ] |
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197: test_ShortReadQ_coerce_DNAStringSet <- function()
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210: test_ShortReadQ_coerce_QualityScaledDNAStringSet <- function()
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11: checkStringSet(sread(obj), "DNAStringSet", len, wd[[2]])
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200: as(ShortReadQ(), "DNAStringSet"),
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201: DNAStringSet(setNames(nm = character()))
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206: checkIdentical(sread(obj), unname(as(obj, "DNAStringSet")))
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207: checkIdentical(as.character(id(obj)), names(as(obj, "DNAStringSet")))
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216: checkIdentical(sread(obj), unname(as(res, "DNAStringSet")))
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224: checkIdentical(sread(obj), unname(as(res, "DNAStringSet")))
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236: checkIdentical(sread(obj), unname(as(res, "DNAStringSet")))
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215: res <- as(obj, "QualityScaledDNAStringSet")
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223: res <- as(obj, "QualityScaledDNAStringSet")
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232: checkException(as(obj, "QualityScaledDNAStringSet"), silent=TRUE)
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235: res <- as(obj, "QualityScaledDNAStringSet")
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genomation:inst/unitTests/test_PatternMatrix.R: [ ] |
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4: test_PatternMatrix_matrix_DNAStringSet = function()
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29: test_PatternMatrix_character_DNAStringSet = function()
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9: windows = as(list(DNAString("AAAGCTAAAGGTAAAGCAAAA"),
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10: DNAString("AAAGCTAAAGGTAAAGCAAAA"),
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11: DNAString("AAAGCTAAAGGTAAAGCAAAA")), "DNAStringSet")
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19: windows = as(list(DNAString("AAAGCTAAAGGTAAAGCAAAA"),
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20: DNAString("AAAGCTAAAGGTAAAGCAAAA"),
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21: DNAString("AAAGCTAAAGGTAAAGCAAAA")), "DNAStringSet")
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33: windows = as(list(DNAString("AAAGCTAAAGGTAAAGCAAAA"),
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34: DNAString("AAAGCTAAAGGTAAAGCAAAA"),
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35: DNAString("AAAGCTAAAGGTAAAGCAAAA")), "DNAStringSet")
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42: windows = as(list(DNAString("NNNNNNNNNNNNNN"),
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43: DNAString("NNNNNNNNNNNNNN")), "DNAStringSet")
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51: windows = as(list(DNAString("AAAGCTAAAGGTAAAGCAAAA"),
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52: DNAString("AAAGCTAAAGGTAAAGCAAAA"),
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53: DNAString("AAAGCTAAAGGTAAAGCAAAA")), "DNAStringSet")
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7: patterns <- DNAStringSet(c("AAA", "AAA", "AAA"))
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17: patterns <- DNAStringSet(c("AAA", "AAA", "AAA"))
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gmapR:inst/unitTests/test_GmapGenome.R: [ ] |
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1: test_GmapGenome_constructor_DNAStringSet_noCreate <- function() {
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8: test_GmapGenome_constructor_DNAStringSet_create <- function() {
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2: dna <- Biostrings::DNAStringSet("ACTGTGTCAG")
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12: dna <- Biostrings::DNAStringSet(seq)
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46: dna <- Biostrings::DNAStringSet("ACTGTGTCAG")
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47: names(dna) <- "testDNAString"
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100: dna <- Biostrings::DNAStringSet(c(testA = "ACTGTGTCAGTTCATGGGACCGTTGC",
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19: names(dna) <- "sampleDNAStringSet"
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ChIPanalyser:R/GenomicProfileGenericFunctions.R: [ ] |
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203: .scoreDNAStringSet <- function(PWM,DNASequenceSet, strand="+",
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292: if(class(object) == "DNAStringSet"){
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173: sequences <- readDNAStringSet(fileame)
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hiReadsProcessor:R/hiReadsProcessor.R: [ ] |
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4098: write.listedDNAStringSet <- function(dnaSet, filePath = ".",
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902: #' @param patternSeq DNAString object or a sequence containing the query sequence to search. This is generally smaller than subjec...(7 bytes skipped)...
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1082: #' @param patternSeq DNAString object or a sequence containing the query sequence to search with the primerID.
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1151: pattern1 <- as.character(subseq(DNAString(patternSeq), 1, primerIDpos[1] - 1))
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1152: pattern2 <- as.character(subseq(DNAString(patternSeq),
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1282: #' @param patternSeq DNAString object or a sequence containing the query sequence to search. This is generally smaller than subjec...(7 bytes skipped)...
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1433: #' @param patternSeq DNAString object or a sequence containing the query sequence to search.
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1458: patternSeq.rc <- as.character(reverseComplement(DNAString(patternSeq)))
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3055: #' @param patternSeq DNAString object or a sequence containing the query sequence to search.
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3108: #' @param Vector DNAString object containing vector sequence to be searched in reads.
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3262: stopifnot(class(dnaSet) %in% c("DNAStringSet", "DNAString"))
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4194: if(!grepl("DNAString", class(Vector))) {
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4195: stop("Vector paramter is not of DNAString class")
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414: #' Removes duplicate sequences from DNAStringSet object.
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416: #' Given a DNAStringSet object, the function dereplicates reads and
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419: #' @param dnaSet DNAStringSet object to dereplicate.
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421: #' @return DNAStringSet object with names describing frequency of repeat.
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437: if(!is(dnaSet,"DNAStringSet")) {
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438: dnaSet <- DNAStringSet(dnaSet)
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456: #' Replicate sequences from DNAStringSet object using counts identifier or vector
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458: #' Given a DNAStringSet object, the function replicates reads using counts=X
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461: #' @param dnaSet DNAStringSet object to replicate.
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467: #' @return DNAStringSet object.
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485: stopifnot(is(dnaSet,"DNAStringSet"))
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512: #' Given a DNAStringSet object, the function removes any reads that has either repeating or total Ns which is greater th...(21 bytes skipped)...
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514: #' @param dnaSet DNAStringSet object to evaluate.
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519: #' @return DNAStringSet object.
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533: if(!is(dnaSet,"DNAStringSet")) {
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534: dnaSet <- DNAStringSet(dnaSet)
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568: #' chunkize(DNAStringSet(x), 5)
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580: #' Split DNAStringSet object using first X number of bases defined by a vector.
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582: #' Given a character vector of barcodes/MID to sample association and a DNAStringSet object, the function splits/demultiplexes the DNAStringSet object by first few bases dictated by length of barcodes/MID supplied. This is an accessory func...(39 bytes skipped)...
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586: #' @param dnaSet DNAStringSet object to evaluate.
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594: #' @return DNAStringSet object split by sample name found in barcodesSample.
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602: #' dnaSet <- DNAStringSet(c("read1" = "ACATCCATAGAGCTACGACGACATCGACATA",
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645: unmatched <- DNAStringSet(dnaSet[!good.row])
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646: dnaSet <- DNAStringSet(dnaSet[good.row], start = trimFrom)
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678: #' @param dnaSet DNAStringSet object containing sequences to be decoded or
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697: #' appeneded to respective sample slots, else a named list of DNAStringSet
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709: #' dnaSet <- DNAStringSet(c("read1" = "ACATCCATAGAGCTACGACGACATCGACATA",
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901: #' @param subjectSeqs DNAStringSet object containing sequences to be searched for the pattern. This is generally bigger than patter...(94 bytes skipped)...
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952: #' subjectSeqs <- DNAStringSet(xscat("AAAAAAAAAA", subjectSeqs))
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989: badSeqs <- DNAStringSet()
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1081: #' @param subjectSeqs DNAStringSet object containing sequences to be searched for the pattern.
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1121: #' primerIDAlignSeqs(DNAStringSet(subjectSeqs), patternSeq, doAnchored = TRUE)
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1281: #' @param subjectSeqs DNAStringSet object containing sequences to be searched for the pattern. This is generally bigger than patter...(94 bytes skipped)...
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1316: #' subjectSeqs <- DNAStringSet(xscat("AAAAAAAAAA", subjectSeqs))
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1334: badSeqs <- DNAStringSet()
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1432: #' @param subjectSeqs DNAStringSet object containing sequences to be searched for the pattern.
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3056: #' @param subjectSeqs DNAStringSet object containing sequences to be searched for the pattern.
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3062: #' @return DNAStringSet object with pattern sequence removed from the subject sequences.
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3074: #' subjectSeqs=DNAStringSet(c("AGACCCTTTTGAGCAGCAT","AGACCCTTGGTCGACTCA",
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3107: #' @param reads DNAStringSet object containing sequences to be trimmed for vector.
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3115: #' @return DNAString...(202 bytes skipped)... region and whether it was considered valid denoted by 'good.row'. The second element, "reads" is a DNAStringSet object with Vector sequence removed from the reads.
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3238: #' This function trims a DNAStringSet object using the ranges from left, right, or middle of the sequence. This is a helper function u...(202 bytes skipped)...
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3240: #' @param dnaSet DNAStringSet object containing sequences to be trimmed.
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3245: #' @return a DNAStringSet object with trimmed sequences.
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3254: #' dnaSet <- DNAStringSet(c("AAAAAAAAAACCTGAATCCTGGCAATGTCATCATC",
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3358: #' @return a listed DNAStringSet object structed by sector then sample.
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3917: #' Given a sequence reads file path, the function returns a DNAStringSet object.
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3925: #' @return if isPaired is FALSE, then a DNAStringSet object, else a list of
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3926: #' DNAStringSet objects of three elements corresponding to reads from
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4054: #' Given a listed DNAStringSet object return from \code{\link{extractSeqs}}, the
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4057: #' @param dnaSet listed DNAStringSet object containing sequences to be written.
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4583: #' Align a listed DNAStringSet to a reference using gfClient or standalone BLAT.
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4585: #' Align sequences from a listed DNAStringSet object returned from
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4591: #' @param dnaSetList DNAStringSet object containing sequences to be aligned against the reference.
|
4605: stop("dnaSetList is empty. Please supply a listed DNAStringSet ",
|
4666: #' Given a vector of sequences or DNAStringSet or a FASTA filename, the function
|
4669: #' @param x a DNAStringSet object, or a FASTA filename.
|
4672: #' @param filename name of the file if x is a DNAStringSet object.
|
4683: #' seqs <- DNAStringSet(sapply(sample(c(100:1000), 500),
|
4706: } else if (class(x) == "DNAStringSet") {
|
4737: #' @param query an object of DNAStringSet, a character vector of filename(s),
|
4739: #' @param subject an object of DNAStringSet, a character vector, or a path to
|
4845: subject <- DNAStringSet(subject)
|
4850: ## subjectFile is still null so it means that subject is a DNAStringSet
|
4889: query <- DNAStringSet(query)
|
4894: ## queryFiles is still null so it means that query is a DNAStringSet
|
6334: } else if(is(x, "DNAStringSet")) {
|
6533: #' Prepend name attribute of a list to DNAStringSet
|
6535: #' Given a named listed DNAStringSet object returned from \code{\link{extractSeqs}},
|
6541: #' @return listed DNAStringSet with the names attribute prepended with the
|
6542: #' name of the list. If flatten is TRUE, then a DNAStringSet object
|
6560: if(all(sapply(dnaSet, class)=="DNAStringSet")) {
|
6561: ## this would be list of DNAStringSets ##
|
2396: Vector <- readDNAStringSet(vectorFile)
|
2633: write.listedDNAStringSet(seqs, filePrefix = paste0("processed", f))
|
2644: write.listedDNAStringSet(seqs, filePrefix = paste0("processed", f))
|
2650: write.listedDNAStringSet(seqs, filePrefix = paste0("processed", f))
|
4001: dnaSet <- readDNAStringSet(x, format = 'fastq')
|
4034: dnaSet <- readDNAStringSet(seqFilePath)
|
4096: #' write.listedDNAStringSet(seqs)
|
6545: #' \code{\link{getSectorsForSamples}}, \code{\link{write.listedDNAStringSet}}
|
sangeranalyseR:R/UtilitiesFunc.R: [ ] |
---|
191: fRDNAStringSet <- lapply(forwardReadList, function(forwardRead) {
|
200: rRDNAStringSet <- lapply(reverseReadList, function(reverseRead) {
|
440: primarySeq <- DNAString(paste(primary, collapse=""))
|
441: secondarySeq <- DNAString(paste(secondary, collapse=""))
|
444: primarySeq <- DNAString(paste(primary, collapse=""))
|
445: secondarySeq <- DNAString(paste(secondary, collapse=""))
|
550: DNASeqshift0 <- DNAString(substr(as.character(primarySeq),
|
558: DNASeqshift1 <- DNAString(substr(as.character(primarySeq),
|
566: DNASeqshift2 <- DNAString(substr(as.character(primarySeq),
|
49: ### Creating SangerContigList DNAStringSet
|
55: SangerContigDNASet <- DNAStringSet(SangerContigDNAList)
|
213: ### DNAStringSet storing forward & reverse reads ! (Origin)
|
215: frReadSet <- DNAStringSet(c(unlist(fRDNAStringSet),
|
342: aln2 = c(aln, DNAStringSet(consensus))
|
345: consensusGapfree = RemoveGaps(DNAStringSet(consensus))[[1]]
|
216: unlist(rRDNAStringSet)))
|
217: frReadFeatureList <- c(rep("Forward Reads", length(fRDNAStringSet)),
|
218: rep("Reverse Reads", length(rRDNAStringSet)))
|
crisprDesign:R/utils.R: [ ] |
---|
96: .isDNAStringSet <- function(x){
|
336: if (methods::is(seq, "DNAString") && (is.null(len) || len == 1)){
|
97: methods::is(x, "DNAStringSet")
|
340: if (is(seq, "DNAStringSet") && (is.null(len) || length(seq) == len)){
|
391: #' @importFrom Biostrings DNAStringSet reverseComplement
|
393: x <- Biostrings::DNAStringSet(x)
|
BSgenome:R/getSeq-methods.R: [ ] |
---|
229: .listOfDNAStringToDNAStringSet <- function(x)
|
225: ### Assumes 'x' is a list of DNAString objects and turns it into a
|
351: return(ans[[1L]]) # turn 1st and unique element into DNAString
|
152: return(DNAStringSet())
|
187: unsplit_list_of_XVectorList("DNAStringSet", dnaset_list,
|
226: ### DNAStringSet object.
|
228: ### efficient). Also maybe make this a "DNAStringSet" method for list objects.
|
232: return(DNAStringSet())
|
234: DNAStringSet(successiveViews(subject, elementNROWS(x)))
|
331: ans <- rep.int(DNAStringSet(""), length(sseq_idx))
|
265: .listOfDNAStringToDNAStringSet(ans)
|
VariantAnnotation:R/AllUtilities.R: [ ] |
---|
93: .toDNAStringSetList <- function(x)
|
91: ## DNAStringSetList. Used in predictCoding(), genotypeToSnpMatrix()
|
99: relist(DNAStringSet(xx), pbw)
|
103: ## a DNAStringSetList. Used in .scanVcfToVCF().
|
114: relist(DNAStringSet(flat), x)
|
285: mcols(res) <- DataFrame(REF=DNAStringSet(), ALT=DNAStringSetList(),
|
286: varAllele=DNAStringSet(), CDSLOC=IRanges(),
|
genomation:R/patternMatrix.R: [ ] |
---|
73: .patternPWM_windowsDNAStringSet2matrix = function(pattern, windows,
|
122: .patterncharacter_windowsDNAStringSet2matrix = function(pattern, windows, cores){
|
121: # pattern: character, windows: DNAStringSet
|
127: # regionsSeq <- DNAStringSet(gsub("N", "+", regionsSeq)),
|
199: #' @param windows \code{\link{GRanges}} object or \code{\link{DNAStringSet}} object
|
214: #' a list of sequences (a DNAStringSet object)
|
216: #' in sequences (a DNAStringSet object).
|
228: #' windows = DNAStringSet(seqs)
|
247: #' @aliases patternMatrix,character,DNAStringSet-method
|
249: #' @usage \\S4method{patternMatrix}{character,DNAStringSet}(pattern, windows,
|
252: signature(pattern = "character", windows = "DNAStringSet"),
|
287: stop("All sequences in the input DNAStringSet must have the same
|
300: # pattern: character, windows: DNAStringSet
|
305: #' @aliases patternMatrix,matrix,DNAStringSet-method
|
307: #' @usage \\S4method{patternMatrix}{matrix,DNAStringSet}(pattern, windows,
|
311: signature(pattern = "matrix", windows = "DNAStringSet"),
|
315: stop("All sequences in the input DNAStringSet must have the same
|
336: stop("All sequences in the input DNAStringSet must have the same
|
355: # pattern: matrix, windows: DNAStringSet
|
361: #' @aliases patternMatrix,list,DNAStringSet-method
|
363: #' @usage \\S4method{patternMatrix}{list,DNAStringSet}(pattern, windows,
|
367: signature(pattern = "list", windows = "DNAStringSet"),
|
266: mat <- .patterncharacter_windowsDNAStringSet2matrix(pattern, windows, cores=cores)
|
271: function(i) .patterncharacter_windowsDNAStringSet2matrix(pattern[i],
|
319: mat <- .patternPWM_windowsDNAStringSet2matrix(pattern, windows,
|
sangeranalyseR:R/MethodSangerContig.R: [ ] |
---|
211: fRDNAStringSet <- lapply(object@forwardReadList, function(forwardRead) {
|
225: rRDNAStringSet <- lapply(object@reverseReadList, function(reverseRead) {
|
240: frReadSet <- DNAStringSet(c(unlist(fRDNAStringSet),
|
256: writeTarget <- DNAStringSet(object@contigSeq)
|
224: names(fRDNAStringSet) <- basename(names(fRDNAStringSet))
|
239: names(rRDNAStringSet) <- basename(names(rRDNAStringSet))
|
241: unlist(rRDNAStringSet)))
|
rprimer:R/AllClasses.R: [ ] |
---|
307: .toDNAStringSetOligo <- function(x) {
|
314: .toDNAStringSetAssay <- function(x) {
|
34: #' \code{Biostrings::DNAStringSet}
|
51: #' @importClassesFrom Biostrings DNAStringSet
|
89: #' ## Convert an RprimerOligo object to a DNAStringSet
|
94: #' as(x, "DNAStringSet")
|
96: #' ## Convert an RprimerAssay object to a DNAStringSet
|
101: #' as(x, "DNAStringSet")
|
289: setAs("RprimerOligo", "DNAStringSet", \(from) .toDNAStringSetOligo(from))
|
294: setAs("RprimerAssay", "DNAStringSet", \(from) .toDNAStringSetAssay(from))
|
310: Biostrings::DNAStringSet()
|
317: Biostrings::DNAStringSet()
|
320: Biostrings::DNAStringSet() |>
|
325: Biostrings::DNAStringSet()
|
DECIPHER:R/TrimDNA.R: [ ] |
---|
173: myDNAStringSet <- reverse(myDNAStringSet)
|
29: if (is(leftPatterns, "DNAString") ||
|
37: if (is(rightPatterns, "DNAString") ||
|
17: if (!is(myDNAStringSet, "DNAStringSet"))
|
18: stop("myDNAStringSet must be a DNAStringSet.")
|
30: is(leftPatterns, "DNAStringSet")) {
|
33: stop("leftPatterns must be a DNAStringSet or character vector.")
|
38: is(rightPatterns, "DNAStringSet")) {
|
41: stop("rightPatterns must be a DNAStringSet or character vector.")
|
258: myDNAStringSet <- DNAStringSet()
|
1: TrimDNA <- function(myDNAStringSet,
|
25: any(width(myDNAStringSet) != width(quality)))
|
26: stop("The widths of myDNAStringSet must match the widths of quality.")
|
88: left <- numeric(length(myDNAStringSet))
|
94: myDNAStringSet,
|
120: x <- seq_len(length(myDNAStringSet))
|
130: .subset(myDNAStringSet, x),
|
153: lefts <- integer(length(myDNAStringSet))
|
172: dna <- myDNAStringSet
|
182: rights <- width(myDNAStringSet)
|
193: right <- width(myDNAStringSet) - .findPatternEnd(rightPatterns[k])
|
240: ns <- names(myDNAStringSet)
|
243: myDNAStringSet <- dna[w]
|
244: myDNAStringSet <- subseq(myDNAStringSet,
|
248: a <- alphabetFrequency(myDNAStringSet, as.prob=TRUE, baseOnly=TRUE)
|
251: myDNAStringSet <- myDNAStringSet[-x]
|
279: return(myDNAStringSet)
|
282: myDNAStringSet))
|
CNEr:R/utils.R: [ ] |
---|
4: compDNAStringSet <- function(DNAStringSet1, DNAStringSet2){
|
2: ### Compare two DNAStringSet. Match is TRUE, Mismatch is FALSE.
|
5: tmp <- cbind(strsplit(as.character(DNAStringSet1), ""),
|
6: strsplit(as.character(DNAStringSet2), ""))
|
33: seqToAlignment <- function(DNAStringSet){
|
34: foo <- strsplit(as.character(DNAStringSet), "")
|
9: #system.time(foo<-compDNAStringSet(targetSeqs(myAxt), querySeqs(myAxt)))
|
PWMEnrich:man/DNAStringSetToList.Rd: [ ] |
---|
5: \title{Convert DNAStringSet to list of DNAString objects}
|
3: \name{DNAStringSetToList}
|
4: \alias{DNAStringSetToList}
|
7: DNAStringSetToList(x)
|
10: \item{x}{an object of class DNAStringSet}
|
13: as.list doesn't seem to always work for DNAStringSets, so
|
Modstrings:man/ModDNAString.Rd: [ ] |
---|
41: \code{\link{modifyNucleotides}} and modify and existing DNAString or
|
44: A \code{ModDNAString} object can be converted into a \code{DNAString} object
|
63: # convert to DNAString
|
64: d1 <- DNAString(md1)
|
3: \name{ModDNAString}
|
4: \alias{ModDNAString}
|
5: \title{ModDNAString class}
|
7: ModDNAString(x = "", start = 1, nchar = NA)
|
13: the \code{ModDNAString} object (default \code{start = 1}).}
|
16: \code{ModDNAString} object (default \code{nchar = NA}). The end position is
|
20: a \code{ModDNAString} object
|
23: A \code{ModDNAString} object allows DNA sequences with modified nucleotides
|
27: The ModDNAString class contains the virtual \code{\link{ModString}} class,
|
32: The \code{\link{alphabet}} of the ModDNAString class consist of the
|
35: modifications: \code{alphabet(ModDNAString())}.
|
42: ModDNAString object.
|
52: # Constructing ModDNAString containing an m6A
|
53: md1 <- ModDNAString("AGCT`")
|
56: # the alphabet of the ModDNAString class
|
motifcounter:man/generateDNAString.Rd: [ ] |
---|
5: \title{Generate DNAString}
|
15: A DNAString object
|
18: This function generates a random DNAString of a given length
|
3: \name{generateDNAString}
|
4: \alias{generateDNAString}
|
7: generateDNAString(len, bg)
|
31: motifcounter:::generateDNAString(1000, bg)
|
25: seqs = Biostrings::readDNAStringSet(seqfile)
|
35: \code{\link{generateDNAStringSet}}
|
ProteoDisco:R/method_incorporateGenomicMutations.R: [ ] |
---|
217: ...(2 bytes skipped)... Biostrings::substr(CDS.SequenceWT, mut$relativeCDSStart, mut$relativeCDSEnd) == Biostrings::DNAString(mut$refCDS)
|
185: mutsPerCDS$refCDS <- as.character(Biostrings::reverseComplement(Biostrings::DNAStringSet(mutsPerCDS$ref)))
|
186: mutsPerCDS$refAlt <- as.character(Biostrings::reverseComplement(Biostrings::DNAStringSet(mutsPerCDS$alt)))
|
226: CDS.SequenceMut <- Biostrings::DNAStringSet(Biostrings::replaceAt(CDS.SequenceWT, at = IRanges::IRanges(mutsPerCDS$relativeCDSStart, mutsPer...(48 bytes skipped)...
|
241: CDS.SequenceMut <- Biostrings::DNAStringSet(Biostrings::replaceAt(CDS.SequenceWT, at = IRanges::IRanges(mut$relativeCDSStart, mut$relativeCD...(27 bytes skipped)...
|
301: # Add the CDS as names which the DNAStringset inherits.
|
332: mutTx <- Biostrings::DNAStringSet(Biostrings::xscat(base::unlist(Tx.CDS.Current.SequenceWT.tmp)))
|
369: mutTx <- Biostrings::DNAStringSet(Biostrings::xscat(base::unlist(Tx.CDS.Current.SequenceWT.tmp)))
|
412: mutTx <- Biostrings::DNAStringSet(Biostrings::xscat(base::unlist(Tx.CDS.Current.SequenceWT.tmp)))
|
ShortRead:R/methods-QA.R: [ ] |
---|
96: tryCatch(DNAString(Lpattern), error = function(e) {
|
101: tryCatch(DNAString(Rpattern), error = function(e) {
|
Biostrings:src/match_pdict_ACtree2.c: [ ] |
---|
643: subject <- DNAString("TAGTACCAGTTTCGGG")
|
641: dict0 <- DNAStringSet(c("TACCNG", "TAGT", "CGGNT", "AGTAG", "TAGT"))
|
786: * rectangular DNAStringSet object;
|
Motif2Site:R/Motif2Site.R: [ ] |
---|
501: IRanges::ranges(Biostrings::matchPattern(Biostrings::DNAString(motif),
|
509: Biostrings::reverseComplement(Biostrings::DNAString(motif)),
|
538: IRanges::ranges(Biostrings::matchPattern(Biostrings::DNAString(motif),
|
544: Biostrings::reverseComplement(Biostrings::DNAString(motif)),
|
CrispRVariants:R/CrisprSet.R: [ ] |
---|
37: #'@field ref The reference sequence for the target region, as a Biostrings::DNAString object
|
52: #'reference <- Biostrings::DNAString("GGTCTCTCGCAGGATGTTGCTGG")
|
62: ref = "DNAString",
|
968: ins.sites$seq <- as.character(reverseComplement(DNAStringSet(ins.sites$seq)))
|
1092: A DNAStringSet of the consensus sequences for the specified alleles,
|
1168: seqs <- Biostrings::DNAStringSet(seqs)
|
Ularcirc:inst/shiny-app/circRNA/Server.R: [ ] |
---|
1839: circRNA_Sequence <- DNAString(paste(circRNA_Sequence,tmp,sep="",collapse = ""))
|
1842: circRNA_Sequence <- DNAString(circRNA_Sequence)
|
3484: amino_acid_seq <- Biostrings::translate(Biostrings::DNAString(tmp_seq))
|
3895: concat_circRNA <- DNAString(paste(substr(tmp,i,nchar(tmp)),tmp,sep=""))
|
3952: Sequence_to_examine <- DNAString(as.character(to_display[i,1]))
|
3623: Read_One <- DNAStringSet(x=Read_One)
|
3624: Read_Two <- reverseComplement(DNAStringSet(x=Read_Two))
|