Xia Zhao

发表

The first chromosome‐level genome for a marine mammal as a resource to study ecology and evolution

Huanming Yang, Jian Wang, K. Kristiansen, 2019, Molecular ecology resources.

Detection and characterization of copy number variants based on whole-genome sequencing by MGI platforms

Hui Jiang, Junhua Rao, F. Mu, 2019 .

AsmMix: A pipeline for high quality diploid de novo assembly

Hongmei Zhu, Ou Wang, Xia Zhao, 2021, bioRxiv.

Performance assessment of DNA sequencing platforms in the ABRF Next-Generation Sequencing Study

Michael M. Khayat, Wayne E. Clarke, Wenwei Zhang, 2021, Nature Biotechnology.

Development of coupling controlled polymerizations by adapter-ligation in mate-pair sequencing for detection of various genomic variants in one single assay

B. Kermani, Oleg Alferov, A. Alexeev, 2019, DNA research : an international journal for rapid publication of reports on genes and genomes.

Mate-pair Library Construction with Controlled Polymerization Enables Comprehensive Structural Rearrangement Detection

Xun Xu, Kong Xiangdong, Dai Peng, 2018, bioRxiv.

Genome Sequencing Explores Complexity of Chromosomal Abnormalities in Recurrent Miscarriage.

S. Cheung, Yuan Jiang, Huanming Yang, 2019, American journal of human genetics.

Performance of copy number variants detection based on whole-genome sequencing by DNBSEQ platforms

Xin Liu, Hui Jiang, Fang Chen, 2020, BMC Bioinform..

3′ Branch ligation: a novel method to ligate non-complementary DNA to recessed or internal 3′OH ends in DNA or RNA

B. Peters, A. Alexeev, Yuan Jiang, 2018, bioRxiv.

3’ Branch Ligation: A Novel Method to Ligate Non-Complementary DNA to Recessed or Internal 3’OH Ends in DNA or RNA

Ou Wang, Ao Chen, Wenwei Zhang, 2018, bioRxiv.

Advanced Whole Genome Sequencing Using an Entirely PCR-free Massively Parallel Sequencing Workflow

Zhe Lin, Jing Zhao, Yinlong Xie, 2019, bioRxiv.

Influence of sequencing depth on the fidelity and sensitivity of 1%-5% low-frequency mutation detection and recommendation for standardization of sequencing depth

Hui Jiang, Jun Xia, Xia Zhao, 2021, bioRxiv.

Reliable multiplex sequencing with rare index mis-assignment on DNB-based NGS platform

Yuan Jiang, J. Liu, R. Drmanac, 2018, bioRxiv.

Reliable multiplex sequencing with rare index mis-assignment on DNB-based NGS platform

Jian Wang, Xun Xu, Hui Jiang, 2018, BMC Genomics.

Novel target capture DNA library preparation method using CircLigase-mediated hook ligation.

Xiuqing Zhang, Jiang Yuan, Ao Chen, 2020, New biotechnology.

SLR-superscaffolder: a de novo scaffolding tool for synthetic long reads using a top-to-bottom scheme

Xia Zhao, Ou Wang, Guangyi Fan, 2019, bioRxiv.