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Genome Biology
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June 13, 2025
cuteFC: regenotyping structural variants through an accurate and efficient force-calling method
Tao Jiang, Shuqi Cao, Yadong Liu, et al.
Bioinformatics (Oxford, England)
|
May 17, 2014
FaSD-somatic: a fast and accurate somatic SNV detection algorithm for cancer genome sequencing data
Weixin Wang, Panwen Wang, Feng Xu, et al.
Genome Biology
|
September 15, 2025
Author Correction: cuteFC: regenotyping structural variants through an accurate and efficient force-calling method
Tao Jiang, Shuqi Cao, Yadong Liu, et al.
Innovation (Cambridge (Mass.))
|
December 13, 2021
Applications and potentials of nanopore sequencing in the (epi)genome and (epi)transcriptome era
Shangqian Xie, Amy Wing-Sze Leung, Zhenxian Zheng, et al.
Nature Communications
|
April 3, 2026
Gungnir codec enabling high error-tolerance and low-redundancy DNA storage through substantial computing power
Jingcheng 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 calling
Zhenxian Zheng, Lei Chen, Junhao Su, et al.
Biomedicines
|
April 13, 2018
Transcriptome Analysis of Acute Phase Liver Graft Injury in Liver Transplantation
Nikki P Lee, Haiyang Wu, Kevin T P Ng, et al.
Briefings in Bioinformatics
|
November 25, 2024
Repun: an accurate small variant representation unification method for multiple sequencing platforms
Zhenxian Zheng, Yingxuan Ren, Lei Chen, et al.
Bioinformatics (Oxford, England)
|
April 12, 2026
Accelerated long-read variant calling with Clair3 for whole-genome sequencing
Zhenxian Zheng, Minggao He, Xian Yu, et al.
BMC Genomics
|
December 22, 2020
MegaPath: sensitive and rapid pathogen detection using metagenomic NGS data
Chi-Ming Leung, Dinghua Li, Yan Xin, et al.
Page
of 10
Search research articles
Search
Showing results (21-30 of 100) with videos related to
Sort By:
Page
of 10
Genome Biology
|
June 13, 2025
cuteFC: regenotyping structural variants through an accurate and efficient force-calling method
Tao Jiang, Shuqi Cao, Yadong Liu, et al.
Bioinformatics (Oxford, England)
|
May 17, 2014
FaSD-somatic: a fast and accurate somatic SNV detection algorithm for cancer genome sequencing data
Weixin Wang, Panwen Wang, Feng Xu, et al.
Genome Biology
|
September 15, 2025
Author Correction: cuteFC: regenotyping structural variants through an accurate and efficient force-calling method
Tao Jiang, Shuqi Cao, Yadong Liu, et al.
Innovation (Cambridge (Mass.))
|
December 13, 2021
Applications and potentials of nanopore sequencing in the (epi)genome and (epi)transcriptome era
Shangqian Xie, Amy Wing-Sze Leung, Zhenxian Zheng, et al.
Nature Communications
|
April 3, 2026
Gungnir codec enabling high error-tolerance and low-redundancy DNA storage through substantial computing power
Jingcheng 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 calling
Zhenxian Zheng, Lei Chen, Junhao Su, et al.
Biomedicines
|
April 13, 2018
Transcriptome Analysis of Acute Phase Liver Graft Injury in Liver Transplantation
Nikki P Lee, Haiyang Wu, Kevin T P Ng, et al.
Briefings in Bioinformatics
|
November 25, 2024
Repun: an accurate small variant representation unification method for multiple sequencing platforms
Zhenxian Zheng, Yingxuan Ren, Lei Chen, et al.
Bioinformatics (Oxford, England)
|
April 12, 2026
Accelerated long-read variant calling with Clair3 for whole-genome sequencing
Zhenxian Zheng, Minggao He, Xian Yu, et al.
BMC Genomics
|
December 22, 2020
MegaPath: sensitive and rapid pathogen detection using metagenomic NGS data
Chi-Ming Leung, Dinghua Li, Yan Xin, et al.
Page
of 10