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different reference genome #13
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If the vcf & BSgenome chromosome names match, try running |
@khb7840 [1] "INFO [2023-04-26 10:38:42] Step 02-4. Filter VCF based on optmized filter parameters." |
Strand bias analysis requires strand specific allele supporting read count in the input. |
Thank you very much for your reply. I run FIREVAT again after setting the strand.bias.analysis = FALSE, but a new error occurred in drawing plot section [1] "INFO [2023-04-27 01:04:36] Step 05. Generate FIREVAT report" Thank you so much for your quick reply!!! |
I'm not sure but it can be a font-related problem (stack-overflow link) |
hello
my reference genome is Ensemble v41 hg38.
but your reference genome is ucsc hg38.
so i changed chromosome annotation according to ucsc chromosome version in my vcf file
<style> </style>(ex) GL383518.1 -> chr1_GL383518v1_alt
but i dont know what to do to solve this error
my code:
results <- RunFIREVAT(vcf.file = sample.vcf.file,
vcf.file.genome = 'hg38', # for mouse variants: 'mm10'
config.file = mutect2.config.file,
df.ref.mut.sigs = GetPCAWGMutSigs(),
target.mut.sigs = GetPCAWGMutSigsNames(),
sequencing.artifact.mut.sigs = PCAWG.All.Sequencing.Artifact.Signatures,
output.dir = output.dir,
objective.fn = Default.Obj.Fn,
num.cores = 2,
ga.pop.size = 100,
ga.max.iter = 5,
ga.run = 5,
perform.strand.bias.analysis = TRUE,
ref.forward.strand.var = "TumorDPRefForward",
ref.reverse.strand.var = "TumorDPRefReverse",
alt.forward.strand.var = "TumorDPAltForward",
alt.reverse.strand.var = "TumorDPAltReverse",
annotate = FALSE)
error:
Error in .getOneSeqFromBSgenomeMultipleSequences(x, names[i], start[i], :
sequence chr not found
In addition: Warning messages:
1: In file.remove(paste0(output.dir, existing.firevat.optimization.log.tsv.file)) :
cannot remove file 'C:/Users/User/Desktop/', reason 'Permission denied'
2: In scan(text = x, what = "character", quiet = TRUE, sep = split.char) :
EOF within quoted string
3: In scan(text = x, what = "character", quiet = TRUE, sep = split.char) :
EOF within quoted string
4: In rbind(c(ID = "FAIL", Description = "Fail the site if all alleles fail but for different reasons." :
number of columns of result is not a multiple of vector length (arg 1)
5: In rbind(c(ID = "AD", Number = "R", Type = "Integer", Description = "Allelic depths for the ref and alt alleles in the order listed" :
number of columns of result is not a multiple of vector length (arg 1)
6: In rbind(c(ID = "AS_FilterStatus", Number = "A", Type = "String", :
number of columns of result is not a multiple of vector length (arg 2)
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