Murong Zhou

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.

CTDP identifies disease-associated cell types using scRNA-seq by integrating Lasso-regularized logistic regression and permutation testing, outperforming existing methods in accuracy and robustness.

HiFiCCL improves ultra-low-coverage genome assembly using high-fidelity long-reads, enhancing structural variant detection and pangenome construction in human and plant datasets.