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Bioinformatics (Oxford, England)|September 24, 2010
FastPval: a fast and memory efficient program to calculate very low P-values from empirical distributionMulin Jun Li, Pak Chung Sham, Junwen WangBriefings in Bioinformatics|June 12, 2014
Exploring the function of genetic variants in the non-coding genomic regions: approaches for identifying human regulatory variants affecting gene expressionMulin Jun Li, Bin Yan, Pak Chung Sham, et al.Nucleic Acids Research|June 1, 2013
GWAS3D: Detecting human regulatory variants by integrative analysis of genome-wide associations, chromosome interactions and histone modificationsMulin Jun Li, Lily Yan Wang, Zhengyuan Xia, et al.Briefings in Bioinformatics|November 22, 2019
Methods and resources to access mutation-dependent effects on cancer drug treatmentHongcheng Yao, Qian Liang, Xinyi Qian, et al.Nature Communications|December 6, 2012
A fast and accurate SNP detection algorithm for next-generation sequencing dataFeng Xu, Weixin Wang, Panwen Wang, et al.Nucleic Acids Research|November 7, 2013
dbPSHP: a database of recent positive selection across human populationsMulin Jun Li, Lily Yan Wang, Zhengyuan Xia, et al.Bioinformatics (Oxford, England)|May 3, 2018
A powerful approach reveals numerous expression quantitative trait haplotypes in multiple tissuesDingge Ying, Mulin Jun Li, Pak Chung Sham, et al.Human Mutation|February 14, 2015
wKGGSeq: A Comprehensive Strategy-Based and Disease-Targeted Online Framework to Facilitate Exome Sequencing Studies of Inherited DisordersMulin Jun Li, Jiaen Deng, Panwen Wang, et al.Nucleic Acids Research|May 18, 2018
GWAS4D: multidimensional analysis of context-specific regulatory variant for human complex diseases and traitsDandan Huang, Xianfu Yi, Shijie Zhang, et al.Briefings in Bioinformatics|February 27, 2018
Evaluation of tools for highly variable gene discovery from single-cell RNA-seq dataShun H Yip, Pak Chung Sham, Junwen WangPageof 67