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Zhenxian Zheng

Showing results (1-10 of 16) with videos related to

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BMC Bioinformatics|August 3, 2023
Boosting variant-calling performance with multi-platform sequencing data using Clair3-MPHuijing Yu, Zhenxian Zheng, Junhao Su, et al.
Bioinformatics Advances|January 29, 2024
ClusterV-Web: a user-friendly tool for profiling HIV quasispecies and generating drug resistance reports from nanopore long-read dataJunhao Su, Shumin Li, Zhenxian Zheng, et al.
Briefings in Bioinformatics|July 18, 2022
Clair3-trio: high-performance Nanopore long-read variant calling in family trios with trio-to-trio deep neural networksJunhao Su, Zhenxian Zheng, Syed Shakeel Ahmed, et al.
Nature Computational Science|January 4, 2024
Symphonizing pileup and full-alignment for deep learning-based long-read variant callingZhenxian Zheng, Shumin Li, Junhao Su, et al.
Nature Communications|April 3, 2026
Gungnir codec enabling high error-tolerance and low-redundancy DNA storage through substantial computing powerJingcheng Zhang, Lei Chen, Jinlin Sun, et al.
Nature Methods|July 1, 2026
ClairS: a deep-learning method for long-read tumor-normal pair somatic small variant callingZhenxian Zheng, Lei Chen, Junhao Su, et al.
Innovation (Cambridge (Mass.))|December 13, 2021
Applications and potentials of nanopore sequencing in the (epi)genome and (epi)transcriptome eraShangqian Xie, Amy Wing-Sze Leung, Zhenxian Zheng, et al.
Nature Communications|November 1, 2025
ClairS-TO: a deep-learning method for long-read tumor-only somatic small variant callingLei Chen, Zhenxian Zheng, Junhao Su, et al.
Briefings in Bioinformatics|November 25, 2024
Repun: an accurate small variant representation unification method for multiple sequencing platformsZhenxian Zheng, Yingxuan Ren, Lei Chen, et al.
Bioinformatics (Oxford, England)|April 12, 2026
Accelerated long-read variant calling with Clair3 for whole-genome sequencingZhenxian Zheng, Minggao He, Xian Yu, et al.
Pageof 2

Showing results (1-10 of 16) with videos related to

Sort By:
Pageof 2
BMC Bioinformatics|August 3, 2023
Boosting variant-calling performance with multi-platform sequencing data using Clair3-MPHuijing Yu, Zhenxian Zheng, Junhao Su, et al.
Bioinformatics Advances|January 29, 2024
ClusterV-Web: a user-friendly tool for profiling HIV quasispecies and generating drug resistance reports from nanopore long-read dataJunhao Su, Shumin Li, Zhenxian Zheng, et al.
Briefings in Bioinformatics|July 18, 2022
Clair3-trio: high-performance Nanopore long-read variant calling in family trios with trio-to-trio deep neural networksJunhao Su, Zhenxian Zheng, Syed Shakeel Ahmed, et al.
Nature Computational Science|January 4, 2024
Symphonizing pileup and full-alignment for deep learning-based long-read variant callingZhenxian Zheng, Shumin Li, Junhao Su, et al.
Nature Communications|April 3, 2026
Gungnir codec enabling high error-tolerance and low-redundancy DNA storage through substantial computing powerJingcheng Zhang, Lei Chen, Jinlin Sun, et al.
Nature Methods|July 1, 2026
ClairS: a deep-learning method for long-read tumor-normal pair somatic small variant callingZhenxian Zheng, Lei Chen, Junhao Su, et al.
Innovation (Cambridge (Mass.))|December 13, 2021
Applications and potentials of nanopore sequencing in the (epi)genome and (epi)transcriptome eraShangqian Xie, Amy Wing-Sze Leung, Zhenxian Zheng, et al.
Nature Communications|November 1, 2025
ClairS-TO: a deep-learning method for long-read tumor-only somatic small variant callingLei Chen, Zhenxian Zheng, Junhao Su, et al.
Briefings in Bioinformatics|November 25, 2024
Repun: an accurate small variant representation unification method for multiple sequencing platformsZhenxian Zheng, Yingxuan Ren, Lei Chen, et al.
Bioinformatics (Oxford, England)|April 12, 2026
Accelerated long-read variant calling with Clair3 for whole-genome sequencingZhenxian Zheng, Minggao He, Xian Yu, et al.
Pageof 2