Author

Hui Huang

BGI Group (China)ORCID 0000-0002-4741-4361Unclaimed ORCID profile · follow to get notified of new preprints

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Hui Huang3 papers · BGI Group (China)

Biology Disciplines

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Genetic & Genomic Medicine· 1 Genetics· 1

Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:statistical model· 2 Research Focus:variant calling· 2 Research Focus:differential expression· 1 Assay:whole-exome sequencing· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Bin Rao· 1 shared Chao CheniD· 1 shared Cheng CheniD· 1 shared Fang CheniD· 1 shared Guoqiang SuniD· 1 shared Haining LuoiD· 1 shared Haisheng Yan· 1 shared Jiale XiangiD· 1 shared

Activity by Year

2018-2020 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 24 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Bin Rao

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2 papers

Recent·Most cited

Genome sequencing combining prenatal ultrasound in the evaluation of fetal CNS structural anomalies

Ying Yang, Sheng Zhao, Guoqiang Sun, Fang Chen, Tongda Zhang, Jieping Song, Wenzhong Yang, Lin Wang, Nianji Zhan, Xiaohong Helena Yang, Xia Zhu, Bin Rao, Zhenzhen Yin, Jing Zhou, Haisheng Yan, , Xinlin Chen

This study evaluates genome sequencing for diagnosing fetal CNS structural anomalies, finding a 38.9% overall diagnostic yield and higher rates in specific malformations.

medRxiv · Mar 4, 2020 · PreprintGenetic & Genomic Medicine

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