Entering edit mode
mlrubio
•
0
@mlrubio-13065
Last seen 7.5 years ago
Hi to all,
When I use ensemblVEP with vep v88 (Running under: Ubuntu 16.04.2 LTS and bioconductor 3.5) to query rs67418256 and VEPParam():
suppressMessages(library(ensemblVEP)) write("rs67418256", file = "example.txt") param_vep <- VEPParam() basic(param_vep)$verbose = FALSE basic(param_vep)$everything=TRUE database(param_vep)$host = "ensembldb.ensembl.org" database(param_vep)$database = FALSE cache(param_vep)$cache = TRUE ensemblVEP(file = "example.txt", param = param_vep)
I obtain the following error:
2017-05-16 19:45:01 - INFO: Database will be accessed when using --hgvs Error: scanVcf: _DNAencode(): invalid DNAString input character: ')' (byte value 41) path: /tmp/RtmpvQCmLN/file621b81eef23
With traceback:
> traceback() 18: stop("scanVcf: ", conditionMessage(err), "\n path: ", file, call. = FALSE) 17: value[[3L]](cond) 16: tryCatchOne(tryCatchList(expr, names[-nh], parentenv, handlers[-nh]), names[nh], parentenv, handlers[[nh]]) 15: tryCatchList(expr, classes, parentenv, handlers) 14: tryCatch({ file <- normalizePath(path.expand(file)) if (!file.exists(file)) stop("file does not exist") maps <- .vcf_scan_header_maps(file, fixed, info, geno, samples, ...) result <- .Call(.scan_vcf_character, file, as.integer(yieldSize), maps$samples, maps$fmap, maps$imap, maps$gmap, row.names) setNames(result, "*:*-*") }, scanTabix_io = function(err) { stop("scanVcf: ", conditionMessage(err), call. = FALSE) }, error = function(err) { stop("scanVcf: ", conditionMessage(err), "\n path: ", file, call. = FALSE) }) 13: .vcf_scan_character(file, ..., fixed = vcfFixed(param), info = vcfInfo(param), geno = vcfGeno(param), samples = vcfSamples(param)) 12: scanVcf(file, param = param, row.names = row.names, ...) 11: scanVcf(file, param = param, row.names = row.names, ...) 10: .scanVcfToVCF(scanVcf(file, param = param, row.names = row.names, ...), file, genome, param) 9: .readVcf(file, genome, param, row.names = row.names, ...) 8: .local(file, genome, param, ...) 7: readVcf(x, "", param = param) 6: readVcf(x, "", param = param) 5: .local(x, VCFRowID, ...) 4: fun(dest, genome = "") 3: fun(dest, genome = "") 2: ensemblVEP(file = "example.txt", param = param_vep) 1: ensemblVEP(file = "example.txt", param = param_vep)
When I run vep
from the command line (in the same system) with the option --everything
I obtain the following result:
rs67418256 6:132376504-132376826 - ENSG00000079931 ENST00000336749 Transcript upstream_gene_variant - - - - - - IMPACT=MODIFIER;DISTANCE=1439;STRAND=-1;VARIANT_CLASS=deletion;SYMBOL=MOXD1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:21063;BIOTYPE=protein_coding;TSL=1;ENSP=ENSP00000336998;SWISSPROT=Q6UVY6;UNIPARC=UPI000013D392
rs67418256 6:132376504-132376826 - ENSG00000079931 ENST00000367963 Transcript intron_variant - - - - - - IMPACT=MODIFIER;STRAND=-1;VARIANT_CLASS=deletion;SYMBOL=MOXD1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:21063;BIOTYPE=protein_coding;CANONICAL=YES;TSL=1;APPRIS=P1;CCDS=CCDS5152.2;ENSP=ENSP00000356940;SWISSPROT=Q6UVY6;UNIPARC=UPI000003F04F;INTRON=1/11;HGVSc=ENST00000367963.7:c.265-2049_265-1727delAAGAAGCTGTAGTTGGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCGGGCGGATCACGAGGTCAGGAGATCGAGACCATCCTGGCTAAAACGGTGAAACCCCGTCTCTACTAAAAATACAAAAAATTAGCCGGGCGTAGTGGCGGGCGCCTGTAGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGAATGGCGTGAACCCGGGAGGCGGAGCTTGCAGTGAGCCGAGATCCCGCCACTGCACTCCAGCCTGGGCGACAGAGCGAGACTCCGTCTCAAAAAAAAAAAAAAAAAAAAAAAAAAAA
Best regards
Miguel Rubio
> sessionInfo() R version 3.4.0 (2017-04-21) Platform: i686-pc-linux-gnu (32-bit) Running under: Ubuntu 16.04.2 LTS Matrix products: default BLAS: /usr/lib/openblas-base/libblas.so.3 LAPACK: /usr/lib/libopenblasp-r0.2.18.so locale: [1] LC_CTYPE=es_ES.UTF-8 LC_NUMERIC=C [3] LC_TIME=es_ES.UTF-8 LC_COLLATE=es_ES.UTF-8 [5] LC_MONETARY=es_ES.UTF-8 LC_MESSAGES=es_ES.UTF-8 [7] LC_PAPER=es_ES.UTF-8 LC_NAME=C [9] LC_ADDRESS=C LC_TELEPHONE=C [11] LC_MEASUREMENT=es_ES.UTF-8 LC_IDENTIFICATION=C attached base packages: [1] stats4 parallel stats graphics grDevices utils datasets [8] methods base other attached packages: [1] ensemblVEP_1.16.0 VariantAnnotation_1.22.0 [3] Rsamtools_1.28.0 Biostrings_2.44.0 [5] XVector_0.16.0 SummarizedExperiment_1.6.1 [7] DelayedArray_0.2.2 matrixStats_0.52.2 [9] Biobase_2.36.2 GenomicRanges_1.28.1 [11] GenomeInfoDb_1.12.0 IRanges_2.10.1 [13] S4Vectors_0.14.1 BiocGenerics_0.22.0 loaded via a namespace (and not attached): [1] Rcpp_0.12.10 AnnotationDbi_1.38.0 GenomicAlignments_1.12.1 [4] zlibbioc_1.22.0 BiocParallel_1.10.1 BSgenome_1.44.0 [7] lattice_0.20-35 tools_3.4.0 grid_3.4.0 [10] DBI_0.6-1 digest_0.6.12 Matrix_1.2-10 [13] GenomeInfoDbData_0.99.0 rtracklayer_1.36.0 bitops_1.0-6 [16] biomaRt_2.32.0 RCurl_1.95-4.8 memoise_1.1.0 [19] RSQLite_1.1-2 compiler_3.4.0 GenomicFeatures_1.28.0 [22] XML_3.98-1.7 >