Author

Jing Cheng

Sichuan UniversityORCID 0000-0002-6145-1003Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

Click to filter author papers

Bioinformatics· 1 Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

Click to filter · or open tag

Organism:human· 2 Assay:whole-genome sequencing· 2 Research Focus:clustering· 1 Approach:deep learning· 1 Research Focus:differential expression· 1 Research Focus:gene regulatory network inference· 1 Approach:statistical model· 1 Research Focus:variant calling· 1

Frequent Co-Authors

Fengxiao BuiD· 2 shared Chao LiuiD· 1 shared Guanglin HeiD· 1 shared Huang SuiD· 1 shared Huijun YuaniD· 1 shared Huijun YuaniD· 1 shared Jie ZhongiD· 1 shared Lan‐Hai WeiiD· 1 shared

Activity by Year

2023-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 37 mutual co-author links

Click any collaborator node to inspect or filter shared papers

Focal author (center)Selected co-authorORCID co-authorUnlinked name

Curved chords = mutual co-authorship

2 shared papersGenetic & Genomic Medicine

Fengxiao BuORCID

Mutual co-authors in cluster

Author profile →

2 papers

Recent·Most cited

Genetic & Genomic MedicinemedRxivPreprintAug 26, 2025

Whole-Genome Sequencing Pilot Study of the Central Asian Genetic Diversity Project Reveals Distinct Genetic Histories, Adaptive Processes, and Introgression Events

Guanglin He, Huang Su, Qiuxia Sun…·Mengge Wang

This study uses whole-genome sequencing of Central Asians to reveal genetic diversity, admixture events, and adaptive processes shaping their demographic history and medical relevance.

1 citation

humanwhole-genome sequencing

𝕏 PostBluesky

BioinformaticsbioRxivPreprintMar 7, 2023

Identification of mobile element insertion from whole genome sequencing data using deep neural network model

Fengxiao Bu, Xiaofei Xu, Yu Huang…·Huijun Yuan

The paper introduces DeepMEI, a deep learning tool for identifying mobile element insertions from whole-genome sequencing data, finding it outperforms existing methods and discovers more non-reference MEIs in 1000 Genome Project samples.

3 citations

humanwhole-genome sequencing

𝕏 PostBluesky