Author

Fei Yang

East China Normal UniversityORCID 0000-0001-8762-8033Unclaimed ORCID profile · follow to get notified of new preprints

Additional preprints under this name without ORCID

Fei Yang5 papers · Kao Corporation (Japan)

Biology Disciplines

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Bioinformatics· 1 Genetic & Genomic Medicine· 1 Genetics· 1

Signature Assays, Organisms & Methods

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Research Focus:benchmarking· 2 Organism:human· 2 Assay:bulk RNA-seq· 1 Assay:CRISPR screen· 1 Research Focus:differential expression· 1 Research Focus:drug response / drug discovery· 1 Approach:experimental assay· 1 Research Focus:gene regulatory network inference· 1

Frequent Co-Authors

Cunbing Xia· 1 shared Dan LiangiD· 1 shared Daniel J. KimiD· 1 shared Dexuan CheniD· 1 shared Dong XuiD· 1 shared Guolong LiuiD· 1 shared Guowei ZhouiD· 1 shared Hai‐Jian SuniD· 1 shared

Activity by Year

2022-2025 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 17 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Cunbing Xia

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3 papers

Recent·Most cited

BioinformaticsbioRxivPreprintNov 9, 2025

Large Language Models for Accessible Reporting of Bioinformatics Analyses in Interdisciplinary Contexts

Lijia Yu, Daniel J. Kim, Yue Cao…·Jean Yee Hwa Yang

This study evaluates how large language models generate summaries of bioinformatics analyses, finding they produce readable and safe summaries but often misinterpret visualizations and lack novel insights.

DOI 10.1101/2025.11.09.687479

machine learning (classical)benchmarking

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Genetic & Genomic MedicinemedRxivPreprintOct 23, 2022

A novel cuproptosis-related gene signature for the prediction of liver cancer prognosis identified DLAT is a potential therapeutic target

Dong Xu, Fei Yang, Yang Chen…·Cunbing Xia

DOI 10.1101/2022.10.23.22280648

humanbulk RNA-seq

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GeneticsbioRxivPreprintSep 5, 2022

Efficient repair of human homozygous genetic mutation by CRISPR/Cas9 mediated interlocus gene conversion

Fei Yang, Jingtao Pang, Guolong Liu…·Yuxuan Wu

This study demonstrates that CRISPR/Cas9-mediated gene conversion can efficiently repair genetic mutations in hematopoietic stem cells without requiring exogenous DNA templates.

DOI 10.1101/2022.09.05.506576

humanCRISPR screen

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