Closed tanger-code closed 11 months ago
Hey, can you check if the contig names match in the FASTA and BAM are chr21? Also were there any log messages?
This is the first 100 lines of the BAM file: chr21_bam_head100.txt And this is the first 100 lines of the ref.fa file: GRCh38_chr21_head100_fa.txt The contig name is both chr21. And there is no error log for GraphTyper.
Is there a problem with my bam file or fasta file?
Sorry, graphtyper won't work with long read data.
Hi, I want to genotyping the chr21 using command:
graphtyper genotype GRCh38#chr21.fa --sam=chr21.sorted.bam --region=chr21
. But there seems to be something wrong with it. The result only contains header.Why does this happen?The ref GRCh38#chr21.fa file that I used contains 2 lines.