Author

Xueqin Guo

BGI Group (China)ORCID 0000-0002-6325-0432Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genomics· 2 Bioinformatics· 1 Genetics· 1

Signature Assays, Organisms & Methods

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Research Focus:database / resource· 2 Approach:experimental assay· 2 Organism:human· 2 Research Focus:differential expression· 1 Research Focus:GWAS / association mapping· 1 Assay:GWAS summary statistics· 1 Approach:statistical model· 1 Research Focus:variant calling· 1

Frequent Co-Authors

Bo Wan· 2 shared Chunhua Peng· 2 shared Cong Hua· 2 shared Fan YangiD· 2 shared Feiyu Zhou· 2 shared Fengzhen CheniD· 2 shared Jia Cai· 2 shared Jiawei Tong· 2 shared

Activity by Year

2019-2020 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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2 shared papersBioinformatics

Bo Wan

Mutual co-authors in cluster

Author profile →

4 papers

Recent·Most cited

VirusDIP: Virus Data Integration Platform

Lina Wang, Fengzhen Chen, Xueqin Guo, Lijin You, Xiaoxia Yang, Fan Yang, Tao Yang, Fei Gao, Cong Hua, Yuantong Ding, Jia Cai, Linlin Yang, Wei E. Huang, Zhicheng Xu, Bo Wan, , Xiaofeng Wei

VirusDIP integrates and provides access to global viral sequence data for analysis and research.

bioRxiv · Jun 8, 2020 · PreprintBioinformatics

CNSA: a data repository for archiving omics data

Xueqin Guo, Fengzhen Chen, Fei Gao, Ling Li, Ke Liu, Lijin You, Cong Hua, Fan Yang, Wanliang Liu, Chunhua Peng, Lina Wang, Xiaoxia Yang, Feiyu Zhou, Jiawei Tong, Jia Cai, , Xun Xu

CNSA provides a data repository for archiving omics data, including raw and analytical data, with a focus on data management and standardization.

Database · Jan 1, 2020Peer-reviewedGenomics

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

Low-frequency variation in TP53 has large effects on head circumference and intracranial volume

Simon J. Haworth, Chin Yang Shapland, Caroline Hayward, Bram Peter Prins, Janine F. Felix, Carolina Medina‐Gómez, Fernando Rivadeneira, Carol A. Wang, Tarunveer S. Ahluwalia, Martine Vrijheid, Mònica Guxens, Jordi Sunyer, Ioanna Tachmazidou, Klaudia Walter, Valentina Iotchkova, , David K. Jackson

The paper identifies 9 novel genetic loci, including low-frequency variants in TP53, associated with head circumference and intracranial volume in up to 46,000 individuals.

Nature Communications · Jan 21, 2019Peer-reviewedGenetics