Author

Renhua Wu

BGI Group (China)ORCID 0000-0002-7070-9707Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:statistical model· 2 Research Focus:variant calling· 2 Assay:whole-exome sequencing· 2 Assay:DNA methylation· 1

Frequent Co-Authors

Chao CheniD· 2 shared Junwei SuniD· 2 shared Zhiyu PengiD· 2 shared Dunjin CheniD· 1 shared Fengyu Guo· 1 shared Haining LuoiD· 1 shared Hui HuangiD· 1 shared Jiale XiangiD· 1 shared

Activity by Year

2018-2019 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 33 mutual co-author links

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2 shared papersGenetics

Chao ChenORCID

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2 papers

Recent·Most cited

Haplotype-Based Noninvasive Prenatal Diagnosis for Duchenne Muscular Dystrophy: A pilot study in South China

Min Chen, Chao Chen, Yingting Li, Yuan Yuan, Zhengfei Lai, Fengyu Guo, Yaoshen Wang, Xiaoyan Huang, Shiquan Li, Renhua Wu, Zhiyu Peng, Junwei Sun, Dunjin Chen

This study demonstrates the feasibility and accuracy of haplotype-based noninvasive prenatal diagnosis for Duchenne Muscular Dystrophy using targeted sequencing in a cohort of at-risk pregnancies.

European Journal of Obstetrics & Gynecology and Reproductive Biology · May 8, 2019Peer-reviewedGenetics

Pre-implantation genetic diagnosis for a family with Usher syndrome through targeted sequencing and haplotype analysis

Haining Luo, Chao Chen, Yun Yang, Yuan Yuan, Wanyang Wang, Renhua Wu, Yinfeng Zhang, Zhiyu Peng, Ying Han, Lu Jiang, Ruqiang Yao, Xiaoying An, Weiwei Zhang, Yanqun Le, Jiale Xiang, , Junwei Sun

This paper applies targeted sequencing and haplotype analysis to develop a PGD assay for Usher syndrome, resulting in a successful pregnancy with a healthy baby.

bioRxiv · Nov 5, 2018 · PreprintGenetics