Luca
04/03/2026, 3:04 PMMaxime Garcia
04/03/2026, 3:06 PMMaxime Garcia
04/03/2026, 3:06 PMLuca
04/03/2026, 3:57 PMIgor Trujnara
04/03/2026, 5:47 PMIgor Trujnara
04/07/2026, 8:14 AMtools: freebayes,strelka,tiddit,cnvkit
skip_tools: baserecalibrator
igenomes_ignore: true
fasta: /path/to/genome.fna
normalize_vcfs: true
snv_consensus_calling: true
consensus_min_count: 2
Some relevant considerations:
• Base recalibration is not available unless you have a known SNP file
• You probably need to download the reference genome, as igenomes has a very limited selection of plants
• All variant callers should work normally, assuming sufficient sequencing data quality
• I have not been able to set up either of the "nice" annotation tools, since databases are not well standardized for plants; you might have to annotate outside sarek
For the VCF, you will get the standard output of the tools, plus a consensus VCF if requested. It should work fine if your plants are diploid, or at least behave like they are. I am not sure what will happen if that is not the case.Luca
04/08/2026, 9:14 AM