View source: R/OverlappingGenes.r
| overlapnearestgeneSearch | R Documentation | 
Extracts gene information from bed files
overlapnearestgeneSearch(
  smap,
  bed,
  inputfmtBed = c("bed", "BNBED"),
  EnzymeType = c("SVMerge", "SE"),
  outpath,
  n = 3,
  returnMethod_bedcomp = c("Text", "dataFrame"),
  input_fmt_SV = c("Text", "dataFrame"),
  bperrorindel = 3000,
  bperrorinvtrans = 50000
)
| smap | character or dataFrame depending on the input_fmt_SV argument. If input_fmt_SV= 'Text", it is path to SMAP file. If input_fmt_SV= 'dataFrame", it is a dataframe. | 
| bed | Text. Normal Bed files or Bionano Bed file. | 
| inputfmtBed | character Whether the bed input is UCSC bed or Bionano bed. Note: extract in bed format to be read by bedsv: awk ' if($3 == "gene" && $13 == "gene_status") print $1,$4,$5,$16,$7 else if ($3 == "gene" && $13 == "gene_name") print $1,$4,$5,$14,$7 ' gencode.v33.annotation.gtf >HomoSapienGRCH19.bed | 
| EnzymeType | Character. Type of enzyme. Options SVMerge and SE. | 
| outpath | character Path for the output files. | 
| n | numeric Number of genes to report which are nearest to the breakpoint. Default is 3. | 
| returnMethod_bedcomp | Character. Type of output Dataframe or in Text format. | 
| input_fmt_SV | Character. Type of output Dataframe or in Text format. | 
| bperrorindel | Numeric. base pair error indel. | 
| bperrorinvtrans | Numeric. base pair error invtranslocation. | 
Data Frame and Text file. Contains the smap with additional Gene Information.
smapName="GM24385_Ason_DLE1_VAP_trio5.smap"
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)
datcomp[1,]
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