SimonaSecomandi
SimonaSecomandi
**1. What were you trying to do?** Call variants from read support. **2. What did you want to happen?** Generate a VCF file. **3. What actually happened?** The command have...
**1. What were you trying to do?** I was trying to performe the augmentation step before variant calling to call variants from a set of illumina WGS reads that I've...
**1. What were you trying to do?** Call variants with vg. I'm trying to align of paired-end illumina reads from different bird individuals to a vg graph generated with the...
Dear all, In the image I’ve attached, there are some SNPs which are confusing to me (the “convoluted” ones). The paths seems to indicate that those are inversions. Indeed, some...
## Issue Description I run the following command which finished successfully but the log says it merged 53 out of 73 files (73%). `pod5 merge -t 32 pod5/*.pod5 -o pod5merged/PAQ83015_bd9104da_d74a1b29.pod5...
**1. What were you trying to do?** I am trying to align short aDNA reads against a Minigraph-Cactus pangenome made of multiple chr-level haplotype-resolved genomes using vg safari. I didn't...
Hi all, I am trying to visualize a small pangenome chunk (368 KB). I have a .vg file and .xg file generated as follows: `vg chunk -t 8 -c 1...