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Seqinfo

A simple S4 class for storing basic information about a collection of genomic sequences

Bioconductor version: 3.23 · Package version: 1.2.0

The Seqinfo class stores the names, lengths, circularity flags, and genomes for a particular collection of sequences. These sequences are typically the chromosomes and/or scaffolds of a specific genome assembly of a given organism. Seqinfo objects are rarely used as standalone objects. Instead, they are used as part of higher-level objects to represent their seqinfo() component. Examples of such higher-level objects are GRanges, RangedSummarizedExperiment, VCF, GAlignments, etc... defined in other Bioconductor infrastructure packages.

Installation

if (!require("BiocManager", quietly = TRUE))
    install.packages("BiocManager")

BiocManager::install("Seqinfo")

Details

MaintainerHervé Pagès <hpages.on.github@gmail.com>
AuthorHervé Pagès [aut, cre] (ORCID: <https://orcid.org/0009-0002-8272-4522>)
LicenseArtistic-2.0
URLhttps://bioconductor.org/packages/Seqinfo
Bug Reportshttps://github.com/Bioconductor/Seqinfo/issues
Downloads rank36567
Source branchRELEASE_3_23
biocViewsAnnotation, DataRepresentation, GenomeAnnotation, GenomeAssembly, Infrastructure, Software

Documentation

Download

Dependencies

Depends: methods, BiocGenerics

Imports: stats, S4Vectors (>= 0.47.6), IRanges

Suggests: GenomeInfoDb, GenomicRanges, BSgenome, GenomicFeatures, TxDb.Hsapiens.UCSC.hg38.knownGene, TxDb.Dmelanogaster.UCSC.dm3.ensGene, BSgenome.Hsapiens.UCSC.hg38, BSgenome.Celegans.UCSC.ce2, RUnit, knitr, rmarkdown, BiocStyle

Reverse dependencies

Depends On Me (19): Biostrings, BSgenome, BSgenomeForge, bumphunter, ChIPComp, CSAR, extraChIPs, GenomeInfoDb, GenomicAlignments, GenomicFeatures, GenomicRanges, GenomicTuples, gmapR, groHMM, HelloRanges, OrganismDbi, Rsamtools, txdbmaker, VariantAnnotation

Imports Me (206): alabaster.ranges, amplican, annoLinker, AnnotationHubData, annotatr, ATACseqTFEA, atena, ballgown, BasicSTARRseq, Bioc.gff, biovizBase, BiSeq, bnbc, branchpointer, bsseq, CAGEfightR, CAGEr, casper, cBioPortalData, CexoR, chipenrich, ChIPexoQual, chromVAR, cleanUpdTSeq, CleanUpRNAseq, cn.mops, CNEr, Cogito, compEpiTools, consensusSeekeR, conumee, crisprBowtie, crisprBwa, crisprDesign, CRISPRseek, crisprShiny, crisprViz, crupR, csaw, DAMEfinder, DaMiRseq, decompTumor2Sig, DegCre, demuxSNP, derfinder, derfinderPlot, DEScan2, DEWSeq, dmGsea, DMRcaller, DMRcate, DMRScan, dmrseq, DominoEffect, easyRNASeq, ELMER, enhancerHomologSearch, ensembldb, EpiCompare, epigraHMM, EpiMix, EpiTxDb, epivizrData, epivizrStandalone, esATAC, FindIT2, FLAMES, G4SNVHunter, GA4GHclient, GA4GHshiny, gcapc, gDNAx, geneAttribution, genomation, GenomAutomorphism, genomeIntervals, GenomicCoordinates, GenomicFiles, GenomicInteractionNodes, GenomicInteractions, GenomicOZone, GenomicPlot, GenomicScores, GenomicState, GenVisR, geomeTriD, ggbio, gmoviz, goseq, GOTHiC, grasp2db, GreyListChIP, Gviz, gwascat, heatmaps, HicAggR, HiCBricks, HiCDOC, HiCExperiment, HiCParser, hicVennDiagram, HiTC, IMAS, InPAS, INSPEcT, InteractionSet, IsoformSwitchAnalyzeR, IVAS, karyoploteR, ldblock, maser, metaseqR2, methInheritSim, methylKit, methylPipe, methylSig, minfi, MinimumDistance, monaLisa, mosaics, motifmatchr, MotifPeeker, motifTestR, MouseFM, msgbsR, multicrispr, MutationalPatterns, MutSeqR, myvariant, NoRCE, nucleR, nullranges, OGRE, OMICsPCA, Organism.dplyr, panelcn.mops, peakCombiner, periodicDNA, PICB, pipeFrame, plyinteractions, plyranges, podkat, pram, prebs, ProteoDisco, PureCN, QDNAseq, qpgraph, qsea, QuasR, r3Cseq, raer, RaggedExperiment, ramr, rCGH, recoup, regioneR, regionReport, REMP, rfPred, RgnTX, RiboCrypt, RiboProfiling, riboSeqR, ribosomeProfilingQC, rigvf, RJMCMCNucleosomes, rnaEditr, RNAmodR, RTCGAToolbox, rtracklayer, scanMiR, scmeth, segmentSeq, SeqArray, seqsetvis, sesame, sesameData, sevenC, SGSeq, ShortRead, sitadela, soGGi, SomaticSignatures, spatzie, SplicingGraphs, SPLINTER, srnadiff, strandCheckR, SummarizedExperiment, svaNUMT, svaRetro, tadar, TCGAutils, TENxIO, TEQC, TFBSTools, trackViewer, transmogR, tRNAscanImport, TVTB, tximeta, VariantFiltering, VplotR, YAPSA

Suggests Me (8): AlphaMissenseR, AnnotationHub, RAIDS, RNAmodR.AlkAnilineSeq, RNAmodR.RiboMethSeq, splicelogic, TFEA.ChIP, TFutils