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Hi.
I'm genotyping SVs in the HG002 sample. The command I used is
for i in {1..22}
do
$graphtyper genotype_sv $ref_file_folder/GCA_chr${i}.fa $vcf_folder/chr${i}_sv/chr${i}.vcf.gz --sam=$bam_file_folder/chr${i}_surject_chr_sort.bam --region=chr${i} --output="graphtyper_chr${i}" &
done
wait
The fasta file I used is : GCA_000001405.15_GRCh38_no_alt_analysis_set.fna.gz.
The vcf file is from : T2TQ100_draftBenchmark.
And I split them up at the chromosomal level.
But the result VCF has some error.
In some records, the REF filed is N, and the ALT filed is not a sequence:
Why does this happen?The fasta file is not N in the corresponding position.
The text was updated successfully, but these errors were encountered:
Hi.
I'm genotyping SVs in the HG002 sample. The command I used is
The fasta file I used is :
GCA_000001405.15_GRCh38_no_alt_analysis_set.fna.gz
.The vcf file is from : T2TQ100_draftBenchmark.
And I split them up at the chromosomal level.
But the result VCF has some error.
In some records, the
REF
filed is N, and theALT
filed is not a sequence:Why does this happen?The
fasta
file is not N in the corresponding position.The text was updated successfully, but these errors were encountered: