View source: R/DGV_extraction.r
| DGVfrequency | R Documentation | 
Frequency calculation of variants compared to DGV.
DGVfrequency(
  hgpath,
  smap,
  smap_data,
  win_indel_DGV = 10000,
  win_inv_trans_DGV = 50000,
  perc_similarity_DGV = 0.5,
  input_fmt_SV = c("Text", "dataframe"),
  returnMethod = c("Text", "dataFrame"),
  outpath,
  EnzymeType = c("SVMerge", "SE")
)
| hgpath | character. Path to Database of Genomic Variants (DGV) Text file. | 
| smap | character. File name for smap textfile. | 
| smap_data | dataframe. Dataset containing smap data. | 
| win_indel_DGV | Numeric. Insertion and deletion error window.Default 10000 bases. | 
| win_inv_trans_DGV | Numeric. Inversion and translocation error window. Default 50000 bases. | 
| perc_similarity_DGV | Numeric . ThresholdPercentage similarity of the query SV and reference SV. Default 0.5. | 
| input_fmt_SV | boolean . Options Text and dataframe. | 
| returnMethod | character. Choice between text or data frame as the output. | 
| outpath | character. Path where gene lists are saved. | 
| EnzymeType | boolean . Options SE and SVMerge. | 
Text and character vector containg gene list and terms associated with them are stored as text files.
hgpath=system.file("extdata", "GRCh37_hg19_variants_2016-05-15.txt", package="nanotatoR")
smappath=system.file("extdata", "GM24385_Ason_DLE1_VAP_trio5.smap", package="nanotatoR")
datDGV <- DGVfrequency (hgpath = hgpath, 
smap = smappath,
win_indel_DGV = 10000,
EnzymeType = "SE", 
input_fmt_SV = "Text",
perc_similarity_DGV = 0.5,returnMethod="dataFrame")
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