Morning! Let's start the day! SVDSS: structural variation discovery in hard-to-call genomic regions using sample-specific strings from accurate long reads by Luca Denti. #RECOMB2023
For now SVDSS can be used to discover insertions and deletions. We have plans to extend its functionalities to other SVs, such as inversions and translocations. Other extensions include somatic SVs discovery and SVs genotyping.
First steps in #pangenomics? Check out our new tutorial!
https://t.co/VlOzRfuZzl
Thanks @jasmijnbaaijens Paola Bonizzoni Christina Boucher @giandellavedova Raffaella Rizzi @jltsiren @PangaiaProject
We have a new preprint out showing that k-mers can be replaced by variable-length strings for the analysis of long and accurate reads (e.g. HiFi)
https://t.co/uUJ1UtVCFC
Joint work with @KhorsandParsoa @BonizzoniPaola@RayanChikhi@DavisCompGen
SFS strings are more expensive to compute than k-mers. In the paper we introduce an heuristic algorithm that finds non-overlapping SFS strings efficiently.