Performance of copy number variants detection based on whole-genome sequencing by DNBSEQ platforms. - Junhua Rao; Lihua Peng; Xinming Liang; Hui Jiang; Chunyu Geng; Xia Zhao; Xin Liu 007; Guangyi Fan; Fang Chen; Feng Mu (BMC Bioinform., 2020)

Accurate haplotype-resolved assembly reveals the origin of structural variants for human trios. - Mengyang Xu; Lidong Guo; Xiao Du; Lei Li; Brock A. Peters; Li Deng; Ou Wang; Fang Chen; Jun Wang 004; Zhesheng Jiang; Jinglin Han; Ming Ni; et al. (Bioinform., 2021)

SLR-superscaffolder: a de novo scaffolding tool for synthetic long reads using a top-to-bottom scheme. - Lidong Guo; Mengyang Xu; Wenchao Wang; Shengqiang Gu; Xia Zhao; Fang Chen; Ou Wang; Xun Xu; Inge Seim; Guangyi Fan; Li Deng; Xin Liu 007 (BMC Bioinform., 2021)

Robust Benchmark Structural Variant Calls of An Asian Using State-of-the-art Long-read Sequencing Technologies. - Xiao Du; Lili Li; Fan Liang; Sanyang Liu; Wenxin Zhang; Shuai Sun; Yuhui Sun; Fei Fan; Linying Wang; Xinming Liang; Weijin Qiu; Guangyi Fan; et al. (Genom. Proteom. Bioinform., 2022)