Comments (7)
Could you check the ALT field? ? do you have a * in there?
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Thanks for your comment.
I have solved the aforementioned issues.
However, I had another issue in using EPO file.
The command line was as followed:
glactools/glactools vcfm2acf --onlyGT --epo all.epo.gz --fai human_g1k_v37.fasta.fai test > test.acf.gz
Then the error message was as followed:
Error, missing data in the EPO file
I wonder if you have any clue what this error message means?
Thanks for your help in advance.
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Is it possible that there is a different encoding of chromosomes? "1" vs "chr1"
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Great!
Removing 'chr' from my VCF file helps and ACF file seems to be made partially.
(Previously, ACF file was not made at all.)
However, the error message pops out after a while.
Could you suggest any other reason for this message?
Thanks in advance.
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just to be sure, are you sure your variants were mapped to hg19/v37? Are there chromosomes that are not 1,2,3..22? did you remove any _random chr? can you do a cut -f 1 |uniq -c on column 1?
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Hello I got an issue
I run vcfm2acf with a merged of multiple vcf files generated by haplotype caller in GATK. and my reference genome was at the scaffold level.
my command:
./glactools vcfm2acf --onlyGT --fai ReferenceGenome.fasta.fai my.vcf > my.acf
but I got this error:
the PL does not have 3,6, or 10 fields, has 1 fields
Does anyone know how to fix this problem?
Best,
BAGUS
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Can you please post a few of the lines that are causing the problem?
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