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NAMESPACE
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NAMESPACE
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import(methods)
importFrom(utils, read.csv, read.table, write.csv, Sweave)
importFrom(grDevices, dev.off, pdf, png, rgb, rainbow)
importFrom(graphics, abline, axis, barplot, hist, legend, lines, mtext, par, plot, points,
polygon, rect, strheight, strwidth, text)
importFrom(stats, as.dist, cutree, filter, hclust)
importFrom(tools, texi2dvi)
importFrom(xtable, xtable)
importFrom(R2HTML, HTML, HTML.title, HTMLEndFile, HTMLInitFile)
importFrom(TeachingDemos, spread.labs)
import(BiocGenerics)
import(S4Vectors)
import(IRanges)
import(XVector)
import(GenomicRanges)
import(SummarizedExperiment)
importClassesFrom(Biobase, AnnotatedDataFrame, AssayData, MIAME, Versions, Versioned, VersionedBiobase, eSet)
importMethodsFrom(Biobase, assayData, "assayData<-", combine, fData, featureData, "featureData<-",
pData, phenoData, "phenoData<-", sampleNames, varMetadata)
importFrom(Biobase, assayDataElementNames, assayDataNew)
importFrom(biomaRt, getBM, getSequence, useMart)
importClassesFrom(Biostrings, DNAString, DNAStringSet, PhredQuality, QualityScaledDNAStringSet,
QualityScaledXStringSet, XStringQuality, XStringSet, BString, SolexaQuality)
importMethodsFrom(Biostrings, PDict, aligned, alphabetFrequency, append, complement,
deletion, endIndex, insertion, matchPDict, matchPattern, mismatchTable,
pairwiseAlignment, quality, reverseComplement, startIndex, translate, vmatchPattern)
importFrom(Biostrings, BStringSet, dinucleotideFrequency, DNAString, DNAStringSet, getSeq,
nucleotideSubstitutionMatrix, oligonucleotideFrequency, PhredQuality, QualityScaledDNAStringSet,
trinucleotideFrequency, writeXStringSet)
importClassesFrom(BSgenome, BSgenome)
importFrom(Rsamtools, scanBam)
importClassesFrom(ShortRead, AlignedRead)
importMethodsFrom(ShortRead, chromosome, id, name, position)
importFrom(ShortRead, AlignedDataFrame, AlignedRead, alignData, sread, alphabetByCycle)
importFrom(VariantAnnotation, VCF, VCFHeader)
importMethodsFrom(VariantAnnotation, writeVcf)
exportClasses(
AVASet,
MapperSet,
AnnotatedVariants,
Breakpoints,
SFFRead,
SFFContainer)
exportMethods(
alignShortReads,
readsOnTarget,
coverageOnTarget,
calculateTiTv,
genomeSequencerMIDs,
sequenceCaptureLinkers,
demultiplexReads,
removeLinker,
filterChimericReads,
detectBreakpoints,
mergeBreakpoints,
annotateVariants,
annotatedVariants,
htmlReport,
ava2vcf,
plotVariationFrequency,
plotAmpliconCoverage,
plotVariants,
plotChimericReads,
seqsC1, "seqsC1<-",
seqsC2, "seqsC2<-",
commonBpsC1, "commonBpsC1<-",
commonBpsC2, "commonBpsC2<-",
commonAlignC1, "commonAlignC1<-",
commonAlignC2, "commonAlignC2<-",
alignedReadsC1, "alignedReadsC1<-",
alignedReadsC2, "alignedReadsC2<-",
MapperSet,
AVASet,
fDataAmp,
featureDataAmp, "featureDataAmp<-",
assayDataAmp, "assayDataAmp<-",
getAlignedReads,
referenceSequences, "referenceSequences<-",
getReadStatus,
getVariantPercentages,
setVariantFilter,
name, "name<-",
flowgramFormat, "flowgramFormat<-",
flowChars, "flowChars<-",
keySequence, "keySequence<-",
clipQualityLeft, "clipQualityLeft<-",
clipQualityRight, "clipQualityRight<-",
clipAdapterLeft, "clipAdapterLeft<-",
clipAdapterRight, "clipAdapterRight<-",
flowgram, "flowgram<-",
flowgrams, "flowgrams<-",
flowIndexes, "flowIndexes<-",
read, "read<-",
quality, "quality<-",
reads, "reads<-",
addRead, getRead,
sff2fastq,
readLengthStats,
readLengthHist,
baseQualityStats,
baseQualityHist,
sequenceQualityHist,
positionQualityBoxplot,
baseFrequency,
nucleotideCharts,
gcContent,
gcPerPosition,
gcContentHist,
complexity.dust,
complexity.entropy,
dinucleotideOddsRatio,
flowgramBarplot,
homopolymerHist
)
export(
extendedCIGARToList,
listToExtendedCIGAR,
readSFF,
writeSFF,
qualityReportSFF
)
useDynLib(R453Plus1Toolbox)