Author

Wei Li

BGI Group (China)ORCID 0000-0002-0693-3536Unclaimed ORCID profile · follow to get notified of new preprints

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Wei Li48 papers · University of California, Irvine

Biology Disciplines

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Signature Assays, Organisms & Methods

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

Frequent Co-Authors

Hao LiiD· 1 shared Hui HuangiD· 1 shared Jianfen Man· 1 shared Jin HuangiD· 1 shared Liangwei MaoiD· 1 shared Lina WangiD· 1 shared Lique Du· 1 shared Long LiiD· 1 shared

Activity by Year

2019-2019 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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1 shared paperGenomics

Hao LiORCID

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1 paper

Recent·Most cited

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