Author

Huajing Teng

Chinese Academy of SciencesORCID 0000-0001-9952-3618Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genomics· 1 Molecular Biology· 1 Systems Biology· 1

Signature Assays, Organisms & Methods

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Research Focus:gene regulatory network inference· 2 Organism:human· 2 Approach:statistical model· 2 Research Focus:benchmarking· 1 Assay:CRISPR screen· 1 Research Focus:database / resource· 1 Assay:DNA methylation· 1 Approach:experimental assay· 1

Frequent Co-Authors

Cheng‐Min ShiiD· 1 shared Fengbiao MaoiD· 1 shared Fengping XuiD· 1 shared Gaoming LiuiD· 1 shared George McDonald ChurchiD· 1 shared Huanming YangiD· 1 shared Hui JiangiD· 1 shared jian Zi WangiD· 1 shared

Activity by Year

2019-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 18 mutual co-author links

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1 shared paperMolecular Biology

Cheng‐Min ShiORCID

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3 papers

Recent·Most cited

Molecular BiologyBiological Journal of the Linnean SocietyPeer-reviewedJul 19, 2023

Asynchronous phylogeographic and demographic dynamics of rodent community in the low latitude Asia

Gaoming Liu, Cheng‐Min Shi, Huajing Teng…·Quansheng Liu

The paper investigates the demographic and phylogeographic dynamics of rodent communities in low latitude Asia, finding asynchronous responses to past climate changes.

DOI 10.1093/biolinnean/blad107

mouseDNA methylation

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Systems BiologybioRxivPreprintMay 20, 2020

Massively parallel quantification of CRISPR editing in cells by TRAP-seq enables better design of Cas9, ABE, CBE gRNAs of high efficiency and accuracy

Xi Xiang, Kunli Qu, Xue Liang…·Yonglun Luo

The paper introduces TRAP-seq to quantify CRISPR editing efficiency and uses it to design improved gRNAs for Cas9, ABE, and CBE with high accuracy and efficiency.

3 citations

humanCRISPR screen

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GenomicsbioRxivPreprintNov 26, 2019

De novo mutations involved in post-transcriptional dysregulation contribute to four neuropsychiatric disorders

Fengbiao Mao, Lu Wang, Xiaolu Zhao…·Zhong Sheng Sun

The paper identifies de novo mutations affecting post-transcriptional regulation that contribute to four neuropsychiatric disorders.

2 citations

humanwhole-exome sequencing

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