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Miaoxin Li

Showing results (41-50 of 71) with videos related to

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Nucleic Acids Research|January 25, 2017
Robust and rapid algorithms facilitate large-scale whole genome sequencing downstream analysis in an integrative frameworkMiaoxin Li, Jiang Li, Mulin Jun Li, et al.
Nucleic Acids Research|July 10, 2019
WITER: a powerful method for estimation of cancer-driver genes using a weighted iterative regression modelling background mutation countsLin Jiang, Jingjing Zheng, Johnny S H Kwan, et al.
Journal of the American Heart Association|October 30, 2017
Dysfunction of Myosin Light-Chain 4 (MYL4) Leads to Heritable Atrial Cardiomyopathy With Electrical, Contractile, and Structural Components: Evidence From Genetically-Engineered RatsWenhui Peng, Miaoxin Li, Hailing Li, et al.
The Journal of Clinical Endocrinology and Metabolism|July 13, 2023
Pigment Epithelium-Derived Factor, a Novel Adipokine, Contributes to Gestational Diabetes MellitusWeiwei Qi, Dan Zhu, Ping Yin, et al.
Bioinformatics (Oxford, England)|August 14, 2018
A powerful conditional gene-based association approach implicated functionally important genes for schizophreniaMiaoxin Li, Lin Jiang, Timothy Shin Heng Mak, et al.
Genome Biology|October 1, 2025
SDFA: a standardized decomposition format and toolkit for efficient analysis of structural variants in large-scale population genomic studiesWenjie Peng, Liubin Zhang, Bin Tang, et al.
Journal of the Peripheral Nervous System : JPNS|April 2, 2009
-459C>T point mutation in 5' non-coding region of human GJB1 gene is linked to X-linked Charcot-Marie-Tooth neuropathyMiaoxin Li, Tat-Sun Cheng, Philip W-L Ho, et al.
Genome Biology|October 30, 2025
Stratifying variant deleteriousness and trait-modulating effect under human recent adaptation using the FIND modelXutong Fan, Dandan Huang, Zhikun Wu, et al.
Genomics, Proteomics & Bioinformatics|December 30, 2025
iRUNNER: A Baseline Mutation Burden Regression for Identifying Gene Interaction Between Rare Variants for DiseasesHui Jiang, Bin Tang, Kun Li, et al.
Bioinformatics (Oxford, England)|June 9, 2016
Predicting regulatory variants with composite statisticMulin Jun Li, Zhicheng Pan, Zipeng Liu, et al.
Pageof 8

Showing results (41-50 of 71) with videos related to

Sort By:
Pageof 8
Nucleic Acids Research|January 25, 2017
Robust and rapid algorithms facilitate large-scale whole genome sequencing downstream analysis in an integrative frameworkMiaoxin Li, Jiang Li, Mulin Jun Li, et al.
Nucleic Acids Research|July 10, 2019
WITER: a powerful method for estimation of cancer-driver genes using a weighted iterative regression modelling background mutation countsLin Jiang, Jingjing Zheng, Johnny S H Kwan, et al.
Journal of the American Heart Association|October 30, 2017
Dysfunction of Myosin Light-Chain 4 (MYL4) Leads to Heritable Atrial Cardiomyopathy With Electrical, Contractile, and Structural Components: Evidence From Genetically-Engineered RatsWenhui Peng, Miaoxin Li, Hailing Li, et al.
The Journal of Clinical Endocrinology and Metabolism|July 13, 2023
Pigment Epithelium-Derived Factor, a Novel Adipokine, Contributes to Gestational Diabetes MellitusWeiwei Qi, Dan Zhu, Ping Yin, et al.
Bioinformatics (Oxford, England)|August 14, 2018
A powerful conditional gene-based association approach implicated functionally important genes for schizophreniaMiaoxin Li, Lin Jiang, Timothy Shin Heng Mak, et al.
Genome Biology|October 1, 2025
SDFA: a standardized decomposition format and toolkit for efficient analysis of structural variants in large-scale population genomic studiesWenjie Peng, Liubin Zhang, Bin Tang, et al.
Journal of the Peripheral Nervous System : JPNS|April 2, 2009
-459C>T point mutation in 5' non-coding region of human GJB1 gene is linked to X-linked Charcot-Marie-Tooth neuropathyMiaoxin Li, Tat-Sun Cheng, Philip W-L Ho, et al.
Genome Biology|October 30, 2025
Stratifying variant deleteriousness and trait-modulating effect under human recent adaptation using the FIND modelXutong Fan, Dandan Huang, Zhikun Wu, et al.
Genomics, Proteomics & Bioinformatics|December 30, 2025
iRUNNER: A Baseline Mutation Burden Regression for Identifying Gene Interaction Between Rare Variants for DiseasesHui Jiang, Bin Tang, Kun Li, et al.
Bioinformatics (Oxford, England)|June 9, 2016
Predicting regulatory variants with composite statisticMulin Jun Li, Zhicheng Pan, Zipeng Liu, et al.
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