View source: R/RNASEQ_Analysis_solo_SVMerge_SE.r
SVexpression_solo | R Documentation |
Annotating the Overlapping and Non-Overlapping genes with RNAseq expression
SVexpression_solo(
input_fmt_SV = c("Text", "dataFrame"),
smapdata,
smappath,
input_fmt_RNASeq = c("Text", "dataFrame"),
RNASeqData,
RNASeqPATH,
outputfmt = c("Text", "datFrame"),
pattern_Proband = NA,
EnzymeType = c("SVMerge", "SE")
)
input_fmt_SV |
character. Input format of the SV data.Options "Text" or "DataFrame". |
smapdata |
dataframe. SV data dataframe. |
smappath |
character. smap path. |
input_fmt_RNASeq |
character. Input format of the RNASeq data. Options "Text" or "DataFrame".. |
RNASeqData |
dataFrame. RNAseq data with gene names. |
RNASeqPATH |
character. RNAseq dataset path . |
outputfmt |
character. Output format of the result. Options "Text" or "DataFrame".. |
pattern_Proband |
character. Pattern for proband. |
EnzymeType |
character. Enzyme used. option "SVMerge" or "SE". |
Dataframe Annotated datafreme with RNASeq data.
RNASeqDir = system.file("extdata", package="nanotatoR")
returnMethod="dataFrame"
datRNASeq <- RNAseqcombine_solo(RNASeqDir = RNASeqDir,
returnMethod = returnMethod)
smapName="NA12878_DLE1_VAP_solo5.smap"
smap = system.file("extdata", smapName, package="nanotatoR")
smap = system.file("extdata", smapName, package="nanotatoR")
bedFile <- system.file("extdata", "HomoSapienGRCH19_lift37.bed", package="nanotatoR")
outpath <- system.file("extdata", package="nanotatoR")
datcomp<-overlapnearestgeneSearch(smap = smap,
bed=bedFile, inputfmtBed = "bed", outpath,
n = 3, returnMethod_bedcomp = c("dataFrame"),
input_fmt_SV = "Text",
EnzymeType = "SE",
bperrorindel = 3000,
bperrorinvtrans = 50000)
datRNASeq1 <- SVexpression_solo (input_fmt_SV=c("dataFrame"),
smapdata = datcomp,
input_fmt_RNASeq=c("dataFrame"),
RNASeqData = datRNASeq,
outputfmt=c("datFrame"),
pattern_Proband = "*_P_*", EnzymeType = c("SE"))
datRNASeq1[1,]
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