Author

Jia Li

BGI Group (China)ORCID 0000-0003-1500-869XUnclaimed ORCID profile · follow to get notified of new preprints

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Jia Li11 papers · Chinese Academy of Sciences

Biology Disciplines

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

Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:statistical model· 2 Assay:whole-exome sequencing· 2 Research Focus:benchmarking· 1 Assay:bulk RNA-seq· 1 Research Focus:differential expression· 1 Research Focus:drug response / drug discovery· 1 Approach:machine learning (classical)· 1

Frequent Co-Authors

Guangshuo CaoiD· 1 shared Hailong HuangiD· 1 shared Haiwei WangiD· 1 shared Hongguo ZhangiD· 1 shared Hua CaoiD· 1 shared Hui Huang· 1 shared Jing He· 1 shared Jing WuiD· 1 shared

Activity by Year

2022-2022 · peak 3/yr

Co-Author Collaboration Network

10 top collaborators · 14 mutual co-author links

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1 shared paperBioinformatics

Guangshuo CaoORCID

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3 papers

Recent·Most cited

BioinformaticsbioRxivPreprintMay 22, 2022

Machine learning enables accurate prediction of breast cancer five-year survival using somatic genomic variants

Xiaosen Jiang, Laizhi Zhang, Guangshuo Cao…·Yong Bai

This study uses machine learning to predict breast cancer five-year survival using somatic genomic variants and phenotype data, achieving an AUC of 0.70 in an external dataset.

DOI 10.1101/2022.05.22.492994

humanwhole-exome sequencing

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Genetic & Genomic MedicineFrontiers in GeneticsPeer-reviewedApr 13, 2022

Whole exome sequencing identifies genes associated with non-obstructive azoospermia

Hongguo Zhang, Hui Huang, Xinyue Zhang…·Ruizhi Liu

The paper identifies five novel genes associated with non-obstructive azoospermia through whole exome sequencing and linkage analysis in a case-control study.

13 citations

humanwhole-exome sequencing

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GeneticsbioRxivPreprintMar 17, 2022

A novel PLS1 c.981+1G>A variant causes autosomal-dominant hereditary hearing loss in a family via up-regulation of the PI3K-Akt signaling pathway

Liangpu Xu, Xinrui Wang, Jia Li…·Hua Cao

The paper identifies a novel PLS1 variant causing autosomal-dominant hearing loss by inducing exon8 skipping and upregulating the PI3K-Akt pathway in zebrafish.

DOI 10.1101/2022.03.17.484618

zebrafishbulk RNA-seq

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