Shuqi Cao

SVPG improves structural variant detection using pangenome references and accelerates pangenome graph construction from long-read data.

This paper introduces SomaSV, a hybrid sequencing framework that improves somatic structural variant detection accuracy while reducing costs by combining long- and short-read data.

The paper introduces cuteSV2, a long-read-based method for accurate structural variant regenotyping, outperforming existing methods in benchmarking.