Parsoa Khorsand

SVDSS improves structural variant discovery in hard-to-call regions using long-read sequencing by combining multiple methodologies, outperforming existing methods in repetitive genomic regions.

Nebula efficiently genotypes structural variants without requiring alignment, outperforming mapping-based methods in speed while maintaining accuracy.

The paper introduces a method to identify sample-specific strings in long-read sequencing data for comparative genome analysis without read mapping.