Author

Teng Zhai

BGI Genomics

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Genetic & Genomic Medicine· 1 Genomics· 1

Signature Assays, Organisms & Methods

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

Frequent Co-Authors

Dongna CheniD· 1 shared Hao LiiD· 1 shared Houxuan LiiD· 1 shared Hui HuangiD· 1 shared Hui HuangiD· 1 shared Huishuang Chen· 1 shared Jianfen Man· 1 shared Jin HuangiD· 1 shared

Activity by Year

2019-2022 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 21 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Dongna ChenORCID

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2 papers

Recent·Most cited

A Novel Gene ZNF862 Causes Hereditary Gingival Fibromatosis

Juan Wu, Dongna Chen, Hui Huang, Ning Luo, Huishuang Chen, Junjie Zhao, Yanyan Wang, Tian Zhao, Siyuan Huang, Yang Ren, Teng Zhai, Weibin Sun, Houxuan Li, Wei Li

The paper identifies a novel heterozygous missense mutation in ZNF862 as the cause of autosomal-dominant non-syndromic hereditary gingival fibromatosis in a Chinese family.

eLife · Feb 10, 2022Peer-reviewedGenetic & Genomic Medicine

Clinical diagnosis of single-gene disorders and chromosomal abnormalities based on BGISEQ-500 platform

Yanqiu Liu, Liangwei Mao, Xiaoming Wei, Jianfen Man, Wenqian Zhang, Lina Wang, Long Li, Yan Sun, Wei Li, Teng Zhai, Xueqin Guo, Lique Du, Jin Huang, Hao Li, Yang Wan, Hui Huang

This study develops a chip-based sequencing method to detect monogenic diseases and chromosomal abnormalities, identifying 102 mutations in 63 patients with 69 new mutations.

bioRxiv · Jun 26, 2019 · PreprintGenomics