The VCF output produced by a command like vg deconstruct -e -a -H '#' ... includes information about the nesting of variants.
With -a, --all-snarls, we obtain not just the top level bubbles, but all nested ones.
This exposed snarl tree information can be used to filter the VCF to obtain a set of non-overlapping sites (n.b. “snarl” is a generic model of graph bubbles including tips and loops).
vcfbub lets us do two common operations on these VCFs:
We can filter sites by maximum level in the snarl tree. For instance, --max-level 0 would keep only sites with LV=0. In practice, vg’s snarl finder ensures that these are sites rooted on the main linear axis of the pangenome graph. Those at higher levels occur within larger variants.
We can filter sites by maximum allele size, either for the reference allele or any allele. In this case, --max-ref-length 10000 would keep only sites where the reference allele is less than 10kb long. Setting --max-ref-length or --max-allele-length additionally ensures that the output contains the bubbles nested inside of any popped bubble, even if they are at greater than --max-level.
vcfbub accomplishes a simple task: we keep sites that are the children of those which we “pop” due to their size.
These occur around complex large SVs, such as multi-Mbp inversions and segmental duplications.
We often need to remove these, as they provide little information for many downstream applications, such as haplotype panels or other imputation references.
usage
This removes all non-top-level variant sites (-l 0) unless they are inside of variants with reference length > 10kb (-r 10000):
vcfbub
popping bubbles in vg deconstruct VCFs
overview
The VCF output produced by a command like
vg deconstruct -e -a -H '#' ...includes information about the nesting of variants. With-a, --all-snarls, we obtain not just the top level bubbles, but all nested ones. This exposed snarl tree information can be used to filter the VCF to obtain a set of non-overlapping sites (n.b. “snarl” is a generic model of graph bubbles including tips and loops).vcfbublets us do two common operations on these VCFs:--max-level 0would keep only sites withLV=0. In practice, vg’s snarl finder ensures that these are sites rooted on the main linear axis of the pangenome graph. Those at higher levels occur within larger variants.--max-ref-length 10000would keep only sites where the reference allele is less than 10kb long. Setting--max-ref-lengthor--max-allele-lengthadditionally ensures that the output contains the bubbles nested inside of any popped bubble, even if they are at greater than--max-level.vcfbubaccomplishes a simple task: we keep sites that are the children of those which we “pop” due to their size. These occur around complex large SVs, such as multi-Mbp inversions and segmental duplications. We often need to remove these, as they provide little information for many downstream applications, such as haplotype panels or other imputation references.usage
This removes all non-top-level variant sites (
-l 0) unless they are inside of variants with reference length > 10kb (-r 10000):