Author

Jianjun Zha

Grandomics (China)

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Bioinformatics· 1 Genetics· 1

Signature Assays, Organisms & Methods

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Research Focus:variant calling· 2 Assay:whole-genome sequencing· 2 Approach:Bayesian inference· 1 Approach:experimental assay· 1 Organism:human· 1 Research Focus:variant effect prediction· 1

Frequent Co-Authors

Changshi Du· 1 shared Cheng YaniD· 1 shared Daoli Yuan· 1 shared Dehua ChengiD· 1 shared Depeng WangiD· 1 shared Dongxue Che· 1 shared Fan LiangiD· 1 shared Ge LiniD· 1 shared

Activity by Year

2020-2024 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 21 mutual co-author links

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1 shared paperBioinformatics

Changshi Du

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2 papers

Recent·Most cited

BayVarC: an ultra-sensitive ctDNA variant caller using Bayesian approach

Dongxue Che, Cheng Yan, Jianjun Zha, Zexiong Niu, Quanyu Yang, Xiaolei Cheng, Mipeng Han, Changshi Du, Ke Zhang, Yun‐Fu Hu, Yu-Fei Yang

BayVarC is a Bayesian variant caller for liquid biopsy that detects low-frequency variants with high sensitivity and low false positive rate.

bioRxiv · Feb 3, 2024 · PreprintBioinformatics

Localization of balanced chromosome translocation breakpoints by long-read sequencing on the Oxford Nanopore platform

Liang Hu, Fan Liang, Dehua Cheng, Zhiyuan Zhang, Guoliang Yu, Jianjun Zha, Yang Wang, Qi Xia, Daoli Yuan, Yue-Qiu Tan, Depeng Wang, Liang Yu, Ge Lin

This study uses Oxford Nanopore long-read sequencing to precisely localize breakpoints in balanced translocations and inversions, achieving single-base resolution for some cases.

Frontiers in Genetics · Jan 14, 2020Peer-reviewedGenetics