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Nucleic Acids Research
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July 10, 2019
WITER: a powerful method for estimation of cancer-driver genes using a weighted iterative regression modelling background mutation counts
Lin Jiang, Jingjing Zheng, Johnny S H Kwan, et al.
Iscience
|
October 21, 2022
Rational drug repositioning for coronavirus-associated diseases using directional mapping and side-effect inference
Jianhua Wang, Jiaojiao Liu, Menghan Luo, et al.
EMBO Reports
|
May 8, 2023
Noncoding SNP at rs1663689 represses ADGRG6 via interchromosomal interaction and reduces lung cancer progression
Xinyue Lei, Xiaoling Tian, Hao Wang, et al.
Genome Biology
|
October 30, 2025
Stratifying variant deleteriousness and trait-modulating effect under human recent adaptation using the FIND model
Xutong Fan, Dandan Huang, Zhikun Wu, et al.
Nucleic Acids Research
|
November 29, 2015
GWASdb v2: an update database for human genetic variants identified by genome-wide association studies
Mulin Jun Li, Zipeng Liu, Panwen Wang, et al.
Nucleic Acids Research
|
May 28, 2020
HRP2-DPF3a-BAF complex coordinates histone modification and chromatin remodeling to regulate myogenic gene transcription
Xu Zhu, Bingxue Lan, Xianfu Yi, et al.
Genomics, Proteomics & Bioinformatics
|
December 30, 2025
iRUNNER: A Baseline Mutation Burden Regression for Identifying Gene Interaction Between Rare Variants for Diseases
Hui Jiang, Bin Tang, Kun Li, et al.
Bioinformatics (Oxford, England)
|
June 9, 2016
Predicting regulatory variants with composite statistic
Mulin Jun Li, Zhicheng Pan, Zipeng Liu, et al.
Iscience
|
April 25, 2023
Systematic fine-mapping and functional studies of prostate cancer risk variants
Yuyang Qian, Jianhua Wang, Bo Wang, et al.
Frontiers in Immunology
|
April 8, 2024
Evaluation of the efficacy and safety of immunotherapy in sarcoma: a two-center study
Zhichao Liao, Jianjin Teng, Tao Li, et al.
Page
of 11
Search research articles
Search
Showing results (51-60 of 107) with videos related to
Sort By:
Page
of 11
Nucleic Acids Research
|
July 10, 2019
WITER: a powerful method for estimation of cancer-driver genes using a weighted iterative regression modelling background mutation counts
Lin Jiang, Jingjing Zheng, Johnny S H Kwan, et al.
Iscience
|
October 21, 2022
Rational drug repositioning for coronavirus-associated diseases using directional mapping and side-effect inference
Jianhua Wang, Jiaojiao Liu, Menghan Luo, et al.
EMBO Reports
|
May 8, 2023
Noncoding SNP at rs1663689 represses ADGRG6 via interchromosomal interaction and reduces lung cancer progression
Xinyue Lei, Xiaoling Tian, Hao Wang, et al.
Genome Biology
|
October 30, 2025
Stratifying variant deleteriousness and trait-modulating effect under human recent adaptation using the FIND model
Xutong Fan, Dandan Huang, Zhikun Wu, et al.
Nucleic Acids Research
|
November 29, 2015
GWASdb v2: an update database for human genetic variants identified by genome-wide association studies
Mulin Jun Li, Zipeng Liu, Panwen Wang, et al.
Nucleic Acids Research
|
May 28, 2020
HRP2-DPF3a-BAF complex coordinates histone modification and chromatin remodeling to regulate myogenic gene transcription
Xu Zhu, Bingxue Lan, Xianfu Yi, et al.
Genomics, Proteomics & Bioinformatics
|
December 30, 2025
iRUNNER: A Baseline Mutation Burden Regression for Identifying Gene Interaction Between Rare Variants for Diseases
Hui Jiang, Bin Tang, Kun Li, et al.
Bioinformatics (Oxford, England)
|
June 9, 2016
Predicting regulatory variants with composite statistic
Mulin Jun Li, Zhicheng Pan, Zipeng Liu, et al.
Iscience
|
April 25, 2023
Systematic fine-mapping and functional studies of prostate cancer risk variants
Yuyang Qian, Jianhua Wang, Bo Wang, et al.
Frontiers in Immunology
|
April 8, 2024
Evaluation of the efficacy and safety of immunotherapy in sarcoma: a two-center study
Zhichao Liao, Jianjin Teng, Tao Li, et al.
Page
of 11