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Genome Biology
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July 17, 2023
Comprehensive analysis of neoantigens derived from structural variation across whole genomes from 2528 tumors
Yang Shi, Biyang Jing, Ruibin Xi
STAR Protocols
|
December 19, 2024
Protocol for directly selecting cell type marker genes for single-cell clustering analyses by Festem
Zihao Chen, Changhu Wang, Ruibin Xi
Current Protocols in Human Genetics
|
October 18, 2012
A survey of copy-number variation detection tools based on high-throughput sequencing data
Ruibin Xi, Semin Lee, Peter J Park
Briefings in Functional Genomics
|
January 11, 2011
Detecting structural variations in the human genome using next generation sequencing
Ruibin Xi, Tae-Min Kim, Peter J Park
Quantitative Biology (Beijing, China)
|
February 12, 2026
Single-cell gene regulatory network analysis for mixed cell populations
Junjie Tang, Changhu Wang, Feiyi Xiao, et al.
Nature Genetics
|
November 29, 2011
Evidence for dosage compensation between the X chromosome and autosomes in mammals
Peter V Kharchenko, Ruibin Xi, Peter J Park
Bioinformatics (Oxford, England)
|
October 17, 2017
SVmine improves structural variation detection by integrative mining of predictions from multiple algorithms
Yuchao Xia, Yun Liu, Minghua Deng, et al.
BMC Bioinformatics
|
April 1, 2017
Pysim-sv: a package for simulating structural variation data with GC-biases
Yuchao Xia, Yun Liu, Minghua Deng, et al.
Cell Reports Methods
|
January 15, 2025
Detecting copy-number alterations from single-cell chromatin sequencing data by AtaCNA
Xiaochen Wang, Zijie Jin, Yang Shi, et al.
BMC Medical Genomics
|
February 2, 2019
Detecting virus integration sites based on multiple related sequencing data by VirTect
Yuchao Xia, Yun Liu, Minghua Deng, et al.
Page
of 7
Search research articles
Search
Showing results (1-10 of 65) with videos related to
Sort By:
Page
of 7
Genome Biology
|
July 17, 2023
Comprehensive analysis of neoantigens derived from structural variation across whole genomes from 2528 tumors
Yang Shi, Biyang Jing, Ruibin Xi
STAR Protocols
|
December 19, 2024
Protocol for directly selecting cell type marker genes for single-cell clustering analyses by Festem
Zihao Chen, Changhu Wang, Ruibin Xi
Current Protocols in Human Genetics
|
October 18, 2012
A survey of copy-number variation detection tools based on high-throughput sequencing data
Ruibin Xi, Semin Lee, Peter J Park
Briefings in Functional Genomics
|
January 11, 2011
Detecting structural variations in the human genome using next generation sequencing
Ruibin Xi, Tae-Min Kim, Peter J Park
Quantitative Biology (Beijing, China)
|
February 12, 2026
Single-cell gene regulatory network analysis for mixed cell populations
Junjie Tang, Changhu Wang, Feiyi Xiao, et al.
Nature Genetics
|
November 29, 2011
Evidence for dosage compensation between the X chromosome and autosomes in mammals
Peter V Kharchenko, Ruibin Xi, Peter J Park
Bioinformatics (Oxford, England)
|
October 17, 2017
SVmine improves structural variation detection by integrative mining of predictions from multiple algorithms
Yuchao Xia, Yun Liu, Minghua Deng, et al.
BMC Bioinformatics
|
April 1, 2017
Pysim-sv: a package for simulating structural variation data with GC-biases
Yuchao Xia, Yun Liu, Minghua Deng, et al.
Cell Reports Methods
|
January 15, 2025
Detecting copy-number alterations from single-cell chromatin sequencing data by AtaCNA
Xiaochen Wang, Zijie Jin, Yang Shi, et al.
BMC Medical Genomics
|
February 2, 2019
Detecting virus integration sites based on multiple related sequencing data by VirTect
Yuchao Xia, Yun Liu, Minghua Deng, et al.
Page
of 7