Description Usage Arguments Value Examples
An integrated function to generate variation-associated database based on sample-specific NGS data or public SNV data.
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vcf |
Input VCF file name. This file contains the information of gene sequence variations. |
annotation |
Input annotation file name. It contains the gene annotation information and can be downloaded from UCSC Genome Browser.Currently it supports RefSeq genes and ENSEMBL genes annotation file. |
refseq |
Input mRNA sequences file with FASTA format. It can be downloaded from UCSC Genome Browser. |
outdir |
Output directory. |
prefix |
The prefix of output file. |
xmx |
The maximum Java heap size. The unit is "G". |
xref |
Optional external cross-reference file,generally it's downloaded through BioMart.If this file is provided,the final html report will present some relevant protein id or description. |
A vector containing two file names. One is a FASTA format file contains the mutated peptides, the normal protein sequences and their reverse versions, and the other is a tab-delimited file contains detailed variation information.
1 2 3 4 5 6 7 8 9 10 11 12 13 | vcf <- system.file("extdata/sapFinder_test.vcf",
package="sapFinder")
annotation <- system.file("extdata/sapFinder_test_ensGene.txt",
package="sapFinder")
refseq <- system.file("extdata/sapFinder_test_ensGeneMrna.fa",
package="sapFinder")
xref <- system.file("extdata/sapFinder_test_BioMart.Xref.txt",
package="sapFinder")
outdir <- "db_dir"
prefix <- "sapFinder_test"
db.files <- dbCreator(vcf=vcf, annotation=annotation,
refseq=refseq, outdir=outdir,
prefix=prefix,xref=xref)
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