Thanks so much Bastien! I added the fasta file and made sure I used tabs. It works now!
Hi there,
I'm trying to manually make a valid vcf file for some indels. I've managed to do so for single nucleotide variations, but indels have failed so far. I check the validity with vcf-validator (https://github.com/EBIvariation/vcf-validator). My output error file is the following for the vcf file I've included as an image here:
According to the VCF specification, the input file is not valid
Error: The header line does not start with the mandatory columns: CHROM, POS, ID, REF, ALT, QUAL, FILTER and INFO. This occurs 1 time(s), first time in line 6.
Warning: A valid 'reference' entry is not listed in the meta section. This occurs 1 time(s), first time in line 6.
Error: Chromosome is not a string without whitespaces, optionally wrapped with angle brackets (<>). This occurs 1 time(s), first time in line 7.
VCF file:
Any guidance would be greatly appreciated!
1 answer
Can we have an example of what is working, to compare too ?
If you do it manually, don't use whitespace between entities, use tabulation.
As you did not include any fasta reference, maybe vcf-validator does not allow chromosome written chr10 but only 10
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