View source: R/RNASEQ_Analysis_Duo_Trio_SVMerge_SE.r
SVexpression_duo_trio | R Documentation |
Extract Read counts for genes that are near or overalapping SVs.
SVexpression_duo_trio(
input_fmt_SV = c("Text", "dataFrame"),
smapdata,
smappath,
input_fmt_RNASeq = c("Text", "dataFrame"),
RNASeqData,
RNASeqPATH,
outputfmt = c("Text", "datFrame"),
pattern_Proband = NA,
pattern_Mother = NA,
pattern_Father = NA,
EnzymeType = c("SVMerge", "SE")
)
input_fmt_SV |
character. genes that are upstream and/or downstream of SV. input_fmt_RNASeq |
smapdata |
dataframe. smap data in dataframe format. |
smappath |
character. smap path. |
input_fmt_RNASeq |
character. input format of RNASEQ data. Text or dataframe. |
RNASeqData |
character. Expression of the genes. |
RNASeqPATH |
character. RNASEQ path. |
outputfmt |
character. Output format choice dataframe or text. |
pattern_Proband |
character. Pattern to identify the proband reads. |
pattern_Mother |
character. Pattern to identify the mother reads. |
pattern_Father |
character. Pattern to identify the father reads. |
EnzymeType |
character. Enzyme used. option "Dual" or "DLE". |
Text or Dataframe containing TPM read counts of genes in the family.
## Not run:
RNASeqDir = system.file("extdata", package="nanotatoR")
returnMethod="dataFrame"
datRNASeq <- RNAseqcombine(RNASeqDir = RNASeqDir,
returnMethod = returnMethod)
smapName="NA12878_DLE1_VAP_solo5.smap"
smap = system.file("extdata", smapName, package="nanotatoR")
datcomp<-overlapnearestgeneSearch(smap = smap,
bed=bedFile, inputfmtBed = "BED", outpath,
n = 3, returnMethod_bedcomp = c("dataFrame"),
input_fmt_SV = "Text",
EnzymeType = "SVMerge",
bperrorindel = 3000,
bperrorinvtrans = 50000)
datRNASeq1 <- SVexpression(
input_fmt_SV=c("dataFrame"),
input_fmt_RNASeq=c("dataFrame"),
RNASeqData = datRNASeq,
outputfmt=c("datFrame"),
pattern_Proband = "*_P_*", EnzymeType = c("SVMerge"))
## End(Not run)
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