Closed idolawoye closed 5 years ago
Hi!
This is probably an upstream problem in the htsjdk library as it can't parse the chromosome name appropriately:
NC_000919.1Treponemapallidumsubsp.pallidumstr.Nicholscompletegenome_pos_[134890,151090]_length_1845
is a bit long for a single chromosome name. Can you please use a FastA reference with shortened chromosome names?
Hello, Sorry to bother once again. I encountered this error whilst using EAGERCLI to process a config file.
#Exception in thread "main" java.io.IOException: Error: Base calls in the vcf file are not sorted! (Note that we currently don't support multiple chromosomes, too!
at VCF2Genome.runUGAnalysis(VCF2Genome.java:209)
at VCF2Genome.<init>(VCF2Genome.java:148)
at VCF2Genome.main(VCF2Genome.java:129)
# The Module VCF2Genome failed in execution at 2019-03-04T14:24:06.613. Check what happened in the logfile.
Kindly assist me with this error. Thanks
Error: Base calls in the vcf file are not sorted! (Note that we currently don't support multiple chromosomes, too!
Do you have more than a single FastA entry in your input reference?
Yes I have two plasmids with the complete genome in the reference file
Well, this isn't supported and since I don't really develop this tool anymore, I won't add that now anymore.
Thanks a lot.
Both sorry and you're welcome 👍
I am trying to run vcf2genome on a vcf file that was produced by GATK using the eager pipeline and it produced this error:
However, my VCF file looks okay and has the #CHROM header as you can see in the attachment. Kindly help out. Thanks :pensive:
SRR3584843_R1.fastq.merged.fq.mappedonly.sorted.cleaned_rmdup.sorted.real.unifiedgenotyper.filtered.vcf.gz](https://github.com/apeltzer/VCF2Genome/files/2888739/SRR3584843_R1.fastq.merged.fq.mappedonly.sorted.cleaned_rmdup.sorted.real.unifiedgenotyper.filtered.vcf.gz)