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Hi,
Thanks for developing this nice tool.
I'd like to use my own fasta and gff to annotate the VCF file, according to the mannual:
grep -v "#" data.gff | sort -k1,1 -k4,4n -k5,5n -t$'\t' | bgzip -c > data.gff.gz tabix -p gff data.gff.gz ./vep -i input.vcf --gff data.gff.gz --fasta genome.fa.gz
Howerver, the output is variant_effect_output.txt, is not VCF file, how can I get the annotated VCF file?
Versions: ensembl : 112.7104005 ensembl-funcgen : 112.be19ffa ensembl-io : 112.2851b6f ensembl-variation : 112.4113356 ensembl-vep : 112.0
Best regards.
The text was updated successfully, but these errors were encountered:
Hi @DayTimeMouse
You can use the --vcf option to output in VCF format. Please see here for more details.
Sorry, something went wrong.
jamie-m-a
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Hi,
Thanks for developing this nice tool.
I'd like to use my own fasta and gff to annotate the VCF file, according to the mannual:
Howerver, the output is variant_effect_output.txt, is not VCF file, how can I get the annotated VCF file?
Best regards.
The text was updated successfully, but these errors were encountered: