Author

Chong Li

Temple UniversityORCID 0000-0002-3802-1507Unclaimed ORCID profile · follow to get notified of new preprints

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Chong Li5 papers · Southwest University

Biology Disciplines

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Signature Assays, Organisms & Methods

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Organism:human· 2 Research Focus:cell type annotation· 1 Approach:deep learning· 1 Approach:experimental assay· 1 Assay:imaging· 1 Research Focus:variant calling· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Aaron M. WengeriD· 1 shared Alex R. HastieiD· 1 shared Alexandra P. LewisiD· 1 shared Allison RegieriD· 1 shared André CorveloiD· 1 shared Anna Okula BasileiD· 1 shared Arvis SulovariiD· 1 shared Ashley D. SandersiD· 1 shared

Activity by Year

2021-2021 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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1 shared paperGenetics

Aaron M. WengerORCID

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2 papers

Recent·Most cited

Variation of female pronucleus reveal oocyte or embryo abnormality: An expert experience deep learning of non-dark box analysis

Jingwei Yang, Yikang Wang, Chong Li, Wei Han, Weiwei Liu, Shun Xiong, Qi Zhang, Keya Tong, Guoning Huang, Xiaodong Zhang

The paper develops a deep learning method to quantify pronuclear (PN) features in embryos and links PN area to chromosomal abnormalities using clinical data.

bioRxiv · Dec 17, 2021 · PreprintGenetics

De novo assembly of 64 haplotype-resolved human genomes of diverse ancestry and integrated analysis of structural variation

Peter Ebert, Peter A. Audano, Qihui Zhu, Bernardo Rodríguez–Martín, David Porubskỳ, Marc Jan Bonder, Arvis Sulovari, Jana Ebler, Weichen Zhou, Rebecca Serra Mari, Feyza Yilmaz, Xuefang Zhao, PingHsun Hsieh, Joyce Lee, Sushant Kumar, , Evan E. Eichler

The paper presents 64 haplotype-resolved human genomes using long-read sequencing and identifies structural variants, SV-eQTLs, and adaptive selection candidates.

Science · Feb 25, 2021Peer-reviewedGenetics