Author

Xiaojun Xu

UC San Diego Health SystemORCID 0000-0003-2548-3304Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1 Genetics· 1

Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:statistical model· 2 Research Focus:variant calling· 2 Assay:whole-exome sequencing· 2 Research Focus:benchmarking· 1 Assay:bulk RNA-seq· 1 Research Focus:GWAS / association mapping· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Olivier HarismendyiD· 2 shared Daniela NachmansoniD· 1 shared Hyunki KimiD· 1 shared Jae Eun LeeiD· 1 shared Jae‐Ho CheongiD· 1 shared Jeong-Hyeon Jo· 1 shared Ji Soo ParkiD· 1 shared Jihoon KimiD· 1 shared

Activity by Year

2017-2021 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 31 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Olivier HarismendyORCID

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2 papers

Recent·Most cited

Genetic & Genomic MedicineScientific ReportsPeer-reviewedJul 20, 2021

Prevalence of cancer susceptibility variants in patients with multiple Lynch syndrome related cancers

Yoon Young Choi, Su‐Jin Shin, Jae Eun Lee…·Olivier Harismendy

The paper identifies pathogenic variants in Lynch Syndrome genes in patients with multiple cancers and finds higher prevalence of non-LS gene variants in early-onset cases.

8 citations

humanwhole-exome sequencing

𝕏 PostBluesky

GeneticsbioRxivPreprintOct 28, 2017

Sharing genetic admixture and diversity of public biomedical datasets

Olivier Harismendy, Jihoon Kim, Xiaojun Xu, Lucila Ohno-machado A

The paper proposes a framework to enrich public biomedical datasets with admixture information and diversity scores, using The Cancer Genome Atlas data to demonstrate its utility.

DOI 10.1101/210716

humanwhole-genome sequencing

𝕏 PostBluesky