| runTandem | R Documentation | 
run X!Tandem
runTandem(spectra = "", fasta = "", outdir = ".", cpu = 1, enzyme = "[KR]|[X]", tol = 10, tolu = "ppm", itol = 0.6, itolu = "Daltons", varmod = NULL, fixmod = NULL, miss = 2, maxCharge = 8, ti = FALSE)
spectra | 
 MS/MS peak list file  | 
fasta | 
 Protein database file for searching.  | 
outdir | 
 The output directory.  | 
cpu | 
 The number of CPU used for X!Tandem search. Default is 1.  | 
enzyme | 
 Specification of specific protein cleavage sites. Default is "[KR]|[X]".  | 
tol | 
 Parent ion mass tolerance (monoisotopic mass).  | 
tolu | 
 Parent ion M+H mass tolerance window units.  | 
itol | 
 Fragment ion mass tolerance (monoisotopic mass).  | 
itolu | 
 Unit for fragment ion mass tolerance (monoisotopic mass).  | 
varmod | 
 Specificiation of potential modifications of residues.  | 
fixmod | 
 Specification of modifications of residues.  | 
miss | 
 The number of missed cleavage sites. Default is 2.  | 
maxCharge | 
 The Maximum parent charge, default is 8  | 
ti | 
 anticipate carbon isotope parent ion assignment errors. Default is false.  | 
The search result file path
vcffile <- system.file("extdata/input", "PGA.vcf",package="PGA")
bedfile <- system.file("extdata/input", "junctions.bed",package="PGA")
gtffile <- system.file("extdata/input", "transcripts.gtf",package="PGA")
annotation <- system.file("extdata", "annotation",package="PGA")
outfile_path<-"db/"
outfile_name<-"test"
library(BSgenome.Hsapiens.UCSC.hg19)
dbfile <- dbCreator(gtfFile=gtffile,vcfFile=vcffile,bedFile=bedfile,
                    annotation_path=annotation,outfile_name=outfile_name,
                    genome=Hsapiens,outdir=outfile_path)
msfile <- system.file("extdata/input", "pga.mgf",package="PGA")
runTandem(spectra = msfile, fasta = dbfile, outdir = "./", cpu = 6,
          enzyme = "[KR]|[X]", varmod = "15.994915@M",
          fixmod = "57.021464@C", tol = 10, tolu = "ppm", itol = 0.05,
          itolu = "Daltons", miss = 2, maxCharge = 8, ti = FALSE)
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