Author

Xueyi Teng

Chinese Academy of SciencesORCID 0000-0001-7258-3477Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Bioinformatics· 1 Genomics· 1 Molecular Biology· 1

Signature Assays, Organisms & Methods

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Organism:human· 3 Research Focus:gene regulatory network inference· 2 Approach:statistical model· 2 Assay:whole-genome sequencing· 2 Assay:bulk RNA-seq· 1 Research Focus:differential expression· 1 Approach:machine learning (classical)· 1 Research Focus:variant calling· 1

Frequent Co-Authors

Huaxia LuoiD· 2 shared Shunmin HeiD· 2 shared Yiwei NiuiD· 2 shared Angela M YuiD· 1 shared Dan Wang· 1 shared Feng QiaoiD· 1 shared Georg SeeligiD· 1 shared Ivan MarazziiD· 1 shared

Activity by Year

2017-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 20 mutual co-author links

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2 shared papersGenomics

Huaxia LuoORCID

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3 papers

Recent·Most cited

Molecular BiologyNature Structural & Molecular BiologyPeer-reviewedDec 1, 2023

The anti-cancer compound JTE-607 reveals hidden sequence specificity of the mRNA 3' processing machinery

Liang Liu, Angela M Yu, Xiuye Wang…·Yongsheng Shi

The paper identifies sequence-specific sensitivity to JTE-607 in mRNA 3' processing by analyzing over 260,000 sequence variants and developing a predictive model.

18 citations

humanyeast

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GenomicsbioRxivPreprintJan 22, 2021

Genome-wide analysis of mobile element insertions in human genomes

Yiwei Niu, Xueyi Teng, Yirong Shi…·Shunmin He

The paper reports a comprehensive map of 36,699 non-reference mobile element insertions (MEIs) from 5,675 human genomes and builds a database for public use.

4 citations

humanwhole-genome sequencing

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BioinformaticsbioRxivPreprintNov 10, 2017

Ennet: construction of potential cancer-driving networks based on somatic enhancer mutations only

Ya Cui, Yiwei Niu, Xueyi Teng…·Runsheng Chen

Ennet identifies cancer-driving networks using somatic enhancer mutations, revealing known and novel networks across multiple cancer types.

DOI 10.1101/216226

humanwhole-genome sequencing

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