Memory efficient string containers, string matching algorithms, and other utilities, for fast manipulation of large biological sequences or sets of sequences.
Author: H. Pagès, P. Aboyoun, R. Gentleman, and S. DebRoy
Maintainer: H. Pagès <hpages.on.github at gmail.com>
To view documentation for the version of this package installed
in your system, start R and enter:
biocViews |
Alignment, DataImport, DataRepresentation, Genetics, Infrastructure, SequenceMatching, Sequencing, Software |
Version |
2.67.0 |
In Bioconductor since |
BioC 1.6 (R-2.1) or earlier (> 17.5 years) |
License |
Artistic-2.0 |
Depends |
R (>= 4.0.0), methods, BiocGenerics(>= 0.37.0), S4Vectors(>= 0.27.12), IRanges(>= 2.31.2), XVector(>= 0.37.1), GenomeInfoDb |
Imports |
methods, utils, grDevices, graphics, stats, crayon |
LinkingTo |
S4Vectors, IRanges, XVector |
Suggests |
BSgenome(>= 1.13.14), BSgenome.Celegans.UCSC.ce2 (>= 1.3.11), BSgenome.Dmelanogaster.UCSC.dm3 (>= 1.3.11), BSgenome.Hsapiens.UCSC.hg18, drosophila2probe, hgu95av2probe, hgu133aprobe, GenomicFeatures(>= 1.3.14), hgu95av2cdf, affy(>= 1.41.3), affydata(>= 1.11.5), RUnit |
SystemRequirements |
|
Enhances |
Rmpi |
URL |
https://bioconductor.org/packages/Biostrings |
BugReports |
https://github.com/Bioconductor/Biostrings/issues |
Depends On Me |
altcdfenvs, amplican, Basic4Cseq, BRAIN, BSgenome, chimeraviz, ChIPanalyser, ChIPsim, cleaver, CODEX, CRISPRseek, DECIPHER, deepSNV, GeneRegionScan, generegulation, GenomicAlignments, GOTHiC, harbChIP, HelloRanges, hiReadsProcessor, iPAC, JASPAR2014, kebabs, MethTargetedNGS, minfi, Modstrings, MotifDb, msa, muscle, NestLink, oligo, ORFhunteR, periodicDNA, pqsfinder, PWMEnrich, qrqc, QSutils, R453Plus1Toolbox, R4RNA, REDseq, rGADEM, RiboProfiling, rRDP, Rsamtools, RSVSim, sangeranalyseR, sangerseqR, SCAN.UPC, SELEX, seqbias, sequencing, ShortRead, SICtools, SimFFPE, ssviz, Structstrings, svaNUMT, systemPipeR, topdownr, TreeSummarizedExperiment, triplex, VarCon |
Imports Me |
AllelicImbalance, alpine, AneuFinder, AnnotationHubData, appreci8R, ArrayExpressHTS, AssessORF, ATACseqQC, BBCAnalyzer, BCRANK, bcSeq, BEAT, BgeeCall, biovizBase, brainflowprobes, branchpointer, BSgenome, bsseq, BUMHMM, BUSpaRse, CellaRepertorium, CellBarcode, ChIPpeakAnno, ChIPseqR, ChIPsim, chromVAR, circRNAprofiler, CircSeqAlignTk, cleanUpdTSeq, cliProfiler, CNEr, CNVfilteR, cogeqc, compEpiTools, consensusDE, coRdon, crisprBase, crisprBowtie, crisprDesign, crisprScore, CrispRVariants, crisprViz, customProDB, dada2, dagLogo, DAMEfinder, decompTumor2Sig, diffHic, DNAshapeR, DominoEffect, easyRNASeq, EDASeq, enhancerHomologSearch, ensembldb, ensemblVEP, EpiTxDb, esATAC, eudysbiome, EventPointer, exomePeak2, factR, FastqCleaner, FLAMES, GA4GHclient, gcapc, gcrma, genbankr, GeneRegionScan, GeneStructureTools, genomation, GenomAutomorphism, GenomicAlignments, GenomicDistributions, GenomicFeatures, GenomicScores, GenVisR, ggbio, ggmsa, girafe, gmapR, gmoviz, GRaNIE, GUIDEseq, Gviz, gwascat, h5vc, heatmaps, HiCDCPlus, HiLDA, HiTC, HTSeqGenie, icetea, idpr, IMMAN, InPAS, IntEREst, InterMineR, IONiseR, ipdDb, IsoformSwitchAnalyzeR, KEGGREST, LinTInd, LowMACA, LymphoSeq, m6Aboost, MADSEQ, MatrixRider, MDTS, MEDIPS, MEDME, memes, MesKit, metaseqR2, methimpute, methylPipe, methylscaper, mia, microbiome, microbiomeDataSets, microbiomeMarker, MicrobiotaProcess, microRNA, MMDiff2, monaLisa, Motif2Site, motifbreakR, motifcounter, motifmatchr, motifStack, MSA2dist, MSnID, MSstatsLiP, MSstatsPTM, multicrispr, MungeSumstats, musicatk, MutationalPatterns, NanoStringNCTools, ngsReports, nucleR, NxtIRFcore, oligoClasses, OmaDB, openPrimeR, ORFik, OTUbase, packFinder, pd.atdschip.tiling, pdInfoBuilder, PhyloProfile, PhyloProfileData, phyloseq, pipeFrame, podkat, polyester, primirTSS, proBAMr, procoil, ProteoDisco, PureCN, Pviz, qPLEXanalyzer, qrqc, qsea, QuasR, r3Cseq, ramwas, RCAS, Rcpi, recoup, regioneR, regutools, REMP, Repitools, RESOLVE, rfaRm, rGADEM, RiboCrypt, ribosomeProfilingQC, RNAmodR, rprimer, Rqc, rtracklayer, sarks, scanMiR, scanMiRApp, scifer, scmeth, SCOPE, scoreInvHap, scPipe, scruff, seqArchR, SeqArray, seqPattern, SGSeq, signeR, SigsPack, single, SingleMoleculeFootprinting, sitadela, SNPhood, soGGi, SomaticSignatures, SparseSignatures, spiky, SpliceWiz, SPLINTER, sscu, StructuralVariantAnnotation, supersigs, surfaltr, svaRetro, synapter, SynExtend, SynMut, syntenet, systemPipeRdata, TAPseq, TarSeqQC, TFBSTools, transite, trena, tRNA, tRNAdbImport, tRNAscanImport, TVTB, txcutr, tximeta, Ularcirc, UMI4Cats, universalmotif, VariantAnnotation, VariantExperiment, VariantFiltering, VariantTools, wavClusteR, XNAString, YAPSA |
Suggests Me |
annotate, AnnotationForge, AnnotationHub, bambu, BANDITS, BeadArrayUseCases, BiocGenerics, BRGenomics, CINdex, CSAR, eisaR, exomeCopy, GenomicFiles, GenomicRanges, GWASTools, HPiP, maftools, methrix, methylumi, MiRaGE, mitoClone2, nuCpos, RNAmodR.AlkAnilineSeq, rpx, rSWeeP, rTRM, spatzie, splatter, systemPipeTools, treeio, tripr, XVector |
Links To Me |
DECIPHER, kebabs, MatrixRider, Rsamtools, ShortRead, triplex, VariantAnnotation, VariantFiltering |
Build Report |
|