This package is for version 3.7 of Bioconductor;
for the stable, up-to-date release version, see
SummarizedExperiment.
The SummarizedExperiment container contains one or more assays, each represented by a matrix-like object of numeric or other mode. The rows typically represent genomic ranges of interest and the columns represent samples.
To view documentation for the version of this package installed
in your system, start R and enter:
biocViews |
Annotation, Coverage, Genetics, GenomeAnnotation, Infrastructure, Sequencing, Software |
Version |
1.10.1 |
In Bioconductor since |
BioC 3.2 (R-3.2) (3 years) |
License |
Artistic-2.0 |
Depends |
R (>= 3.2), methods, GenomicRanges(>= 1.31.17), Biobase, DelayedArray(>= 0.3.20) |
Imports |
utils, stats, tools, Matrix, BiocGenerics(>= 0.15.3), S4Vectors(>= 0.17.25), IRanges(>= 2.13.16), GenomeInfoDb(>= 1.13.1) |
LinkingTo |
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Suggests |
annotate, AnnotationDbi, hgu95av2.db, GenomicFeatures, TxDb.Hsapiens.UCSC.hg19.knownGene, BiocStyle, knitr, rmarkdown, digest, jsonlite, rhdf5, HDF5Array(>= 1.7.5), airway, RUnit |
SystemRequirements |
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Enhances |
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URL |
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Depends On Me |
airway, AllelicImbalance, anamiR, BiocSklearn, BiSeq, bnbc, bsseq, CAGEfightR, clusterExperiment, coseq, csaw, cydar, DaMiRseq, deepSNV, DESeq2, DEXSeq, DiffBind, diffcoexp, diffHic, DMCHMM, DREAM4, dsQTL, ENmix, EnrichmentBrowser, epigenomix, EventPointer, ExpressionAtlas, fission, GenoGAM, GenomicAlignments, GenomicFiles, genoset, geuvPack, GRmetrics, GSEABenchmarkeR, HDCytoData, HelloRanges, hipathia, HMP16SData, InTAD, InteractionSet, IntEREst, iSEE, isomiRs, ivygapSE, JunctionSeq, MBASED, methylPipe, microRNAome, minfi, miRmine, mpra, NADfinder, parathyroidSE, PowerExplorer, recount, REMP, restfulSE, restfulSEData, RIPSeeker, rqt, runibic, sampleClassifierData, Scale4C, scater, scone, scRNAseq, SDAMS, SGSeq, simulatorZ, SingleCellExperiment, singleCellTK, soGGi, stageR, SummarizedBenchmark, TissueEnrich, VanillaICE, VariantAnnotation, yamss, zinbwave |
Imports Me |
adaptest, ALDEx2, alpine, anamiR, anota2seq, apeglm, ASICS, AUCell, BASiCS, BBCAnalyzer, biotmle, biovizBase, BiSeq, BloodCancerMultiOmics2017, brgedata, BUMHMM, CAGEr, CATALYST, ccfindR, CHARGE, ChIPpeakAnno, chromVAR, CLLmethylation, CNPBayes, coexnet, COSMIC.67, DChIPRep, debrowser, DEComplexDisease, DEFormats, DEGreport, DEP, DEScan2, destiny, diffcyt, DominoEffect, easyRNASeq, ELMER, ensemblVEP, epivizrData, erma, FourCSeq, GARS, GenomicDataCommons, GGBase, ggbio, gQTLBase, gQTLstats, GreyListChIP, gwascat, HTSeqGenie, ideal, IHWpaper, ImpulseDE2, InterMineR, iteremoval, LineagePulse, M3D, MADSEQ, MAST, mCSEA, MEAL, MetaNeighbor, methyAnalysis, MethylAid, methylumi, methyvim, MinimumDistance, MLSeq, MoonlightR, motifmatchr, msgbsR, MultiAssayExperiment, MultiDataSet, multiOmicsViz, MutationalPatterns, MWASTools, netSmooth, oligoClasses, omicRexposome, omicsPrint, oncomix, pcaExplorer, phenopath, psichomics, PureCN, R453Plus1Toolbox, RaggedExperiment, RareVariantVis, RcisTarget, readat, regionReport, regsplice, rgsepd, roar, RTCGAToolbox, SC3, scDD, scfind, scmap, scmeth, SCnorm, scoreInvHap, scPipe, scran, semisup, seqCAT, singscore, slalom, SNPchip, SNPhood, splatter, srnadiff, SVAPLSseq, switchde, systemPipeR, TCGAbiolinks, TCGAbiolinksGUI, TCGAutils, TCGAWorkflow, TCGAWorkflowData, TCseq, tenXplore, Trendy, TSRchitect, TTMap, TVTB, TxRegInfra, VariantFiltering, vidger, yriMulti, zFPKM |
Suggests Me |
AnnotationHub, biobroom, biotmleData, DelayedArray, epivizr, epivizrChart, esetVis, GENIE3, GenomicRanges, Glimma, globalSeq, HDF5Array, interactiveDisplay, methyvimData, MSnbase, pathprint, pathprintGEOData, podkat, RforProteomics, RiboProfiling, S4Vectors, scFeatureFilter, TFutils, tissueTreg |
Links To Me |
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Build Report |
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