Description Usage Arguments Value Examples
run X!Tandem
1 2 3 4 |
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
1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 | 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)
|
Add the following code to your website.
For more information on customizing the embed code, read Embedding Snippets.