Author

Chang-Geng Tian

BGI Genomics

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Bioinformatics· 1 Genetics· 1

Signature Assays, Organisms & Methods

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Organism:human· 2 Assay:whole-genome sequencing· 2 Approach:machine learning (classical)· 1 Approach:statistical model· 1 Research Focus:variant calling· 1 Research Focus:variant effect prediction· 1

Frequent Co-Authors

Chao CheniD· 1 shared Chen YeiD· 1 shared Chenghong YiniD· 1 shared Dunjin CheniD· 1 shared Fang CheniD· 1 shared Fanwei Zeng· 1 shared Hankui LiuiD· 1 shared Hao-Xiang Sun· 1 shared

Activity by Year

2020-2020 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 21 mutual co-author links

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1 shared paperGenetics

Chao ChenORCID

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2 papers

Recent·Most cited

BioinformaticsbioRxivPreprintApr 13, 2020

A phenotype-specific framework for identifying the eye abnormalities causative nonsynonymous-variants

Hankui Liu, Xiao Dang, Li-Ping Guan…·Jianguo Zhang

This paper introduces a phenotype-specific framework to identify causative nonsynonymous variants in eye abnormalities, achieving high accuracy and precision in pathogenicity prediction.

2 citations

humanwhole-genome sequencing

𝕏 PostBluesky

GeneticsPrenatal DiagnosisPeer-reviewedJan 9, 2020

Noninvasive Prenatal Diagnosis for Duchenne Muscular Dystrophy Based on the Direct Haplotype Phasing

Min Chen, Chao Chen, Xiaoyan Huang…·Dunjin Chen

This study validates a noninvasive prenatal diagnosis method for Duchenne Muscular Dystrophy using direct haplotype phasing from maternal DNA sequencing.

22 citations

humanwhole-genome sequencing

𝕏 PostBluesky