Author

Fang Chen

BGI Group (China)ORCID 0000-0002-7095-0541Unclaimed ORCID profile · follow to get notified of new preprints

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Fang Chen12 papers · BGI Group (China)

Biology Disciplines

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Bioinformatics· 1 Genetic & Genomic Medicine· 1 Genomics· 1

Signature Assays, Organisms & Methods

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Organism:human· 3 Approach:statistical model· 3 Research Focus:variant calling· 3 Assay:whole-genome sequencing· 2 Research Focus:differential expression· 1 Assay:long-read sequencing· 1

Frequent Co-Authors

Guangyi FaniD· 2 shared Xinming LiangiD· 2 shared Chunyu GengiD· 1 shared Depeng WangiD· 1 shared Dongfang ZouiD· 1 shared Fan LiangiD· 1 shared Fei FaniD· 1 shared Feiqiu WeniD· 1 shared

Activity by Year

2020-2021 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 18 mutual co-author links

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2 shared papersGenomics

Guangyi FanORCID

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3 papers

Recent·Most cited

Clinical and molecular diagnostic study of 320 Chinese children with epilepsy by Genome Sequencing

Dongfang Zou, Lin Wang, Jianxiang Liao, Hongdou Xiao, Jing Duan, Tongda Zhang, Jianbiao Li, Zhenzhen Yin, Jing Zhou, Haisheng Yan, Yushan Huang, Nianji Zhan, Ying Yang, Jingyu Ye, Fang Chen, , Jian Guo

This study evaluates genome sequencing in 320 Chinese children with epilepsy, finding pathogenic variants in 38.13% and demonstrating its diagnostic and therapeutic value.

Brain · Jun 17, 2021Peer-reviewedGenetic & Genomic Medicine

Robust Benchmark Structural Variant Calls of An Asian Using the State-of-Art Long Fragment Sequencing Technologies

Xiao Du, Lili Li, Fan Liang, Sanyang Liu, Wenxin Zhang, Shuai Sun, Yuhui Sun, Fei Fan, Linying Wang, Xinming Liang, Weijin Qiu, Guangyi Fan, Ou Wang, Weifei Yang, Jiezhong Zhang, , Jie Huang

The paper establishes high-confidence structural variant calls in an Asian individual using long-read sequencing technologies and validates them through PCR and Sanger sequencing.

Genomics Proteomics & Bioinformatics · Mar 1, 2021Peer-reviewedGenomics

Detection and characterization of copy number variants based on whole-genome sequencing by DNBSEQ platforms

Junhua Rao, Lihua Peng, Xinming Liang, Hui Jiang, Chunyu Geng, Xia Zhao, Xin Liu, Guangyi Fan, Fang Chen, Feng Mu

This study evaluates CNV detection performance of DNBSEQ and Illumina platforms using WGS data from NA12878, showing DNBSEQ detects more CNVs with similar sensitivity and precision.

BMC Bioinformatics · Nov 11, 2020Peer-reviewedBioinformatics