Description Usage Arguments Details Value Author(s) Examples
Output the non-synonymous SNVs into FASTA file.
1 2 | OutputVarproseq(vartable, proteinseq, outfile, ids, lablersid = FALSE,
RPKM = NULL, ...)
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vartable |
A data frame which is the output of aaVariation(). |
proteinseq |
A dataframe containing protein ids and the protein sequence. |
outfile |
Output file name. |
ids |
A dataframe containing gene/transcript/protein id mapping information. |
lablersid |
If includes the dbSNP rsid in the header of each sequence, default is FALSE. Must provide dbSNP information in function Positionincoding() if put TRUE here. |
RPKM |
If includes the RPKM value in the header of each sequence, default is NULL. |
... |
Additional arguments |
This function uses the output of aaVariation() as input, introduces the nonsynonymous variation into the protein database.
a FASTA file and a data frame containing proteins with single nucleotide variation.
Xiaojing Wang
1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 | vcffile <- system.file("extdata/vcfs", "test1.vcf", package="customProDB")
vcf <- InputVcf(vcffile)
table(GenomicRanges::values(vcf[[1]])[['INDEL']])
index <- which(GenomicRanges::values(vcf[[1]])[['INDEL']] == FALSE)
SNVvcf <- vcf[[1]][index]
load(system.file("extdata/refseq", "exon_anno.RData", package="customProDB"))
load(system.file("extdata/refseq", "dbsnpinCoding.RData", package="customProDB"))
load(system.file("extdata/refseq", "procodingseq.RData", package="customProDB"))
load(system.file("extdata/refseq", "ids.RData", package="customProDB"))
load(system.file("extdata/refseq", "proseq.RData", package="customProDB"))
postable_snv <- Positionincoding(SNVvcf, exon, dbsnpinCoding)
txlist <- unique(postable_snv$txid)
codingseq <- procodingseq[procodingseq$tx_id %in% txlist, ]
mtab <- aaVariation (postable_snv, codingseq)
outfile <- paste(tempdir(), '/test_snv.fasta',sep='')
snvproseq <- OutputVarproseq(mtab, proteinseq, outfile, ids, lablersid=TRUE, RPKM=NULL)
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