SeqCor: correct the effect of gRNA sequences in CRISPR/Cas9 screenings by machine learning algorithm, Xiaojian Liu, Yuanyuan Yang, Yan Qiu, Md. Reyad-ul-ferdous, Qiurong Ding, Yi Wang, 2020
COVID-19 epidemic outside China: 34 founders and exponential growth, Yi Li, Meng Liang, Xianhong Yin, Xiaoyu Liu, Meng Hao, Zixin Hu, Yi Wang, Li Jin, 2020
Robust Reference Powered Association Test of Genome-Wide Association Studies, Wang Y, Li Y, Hao M, Liu X, Zhang M, Wang J, Xiong M, Shugart YY, Jin L, 2019
Nuclear Norm Clustering: a promising alternative method for clustering tasks, Wang Y, Li Y, Qiao C, Liu X, Hao M, Shugart YY, Xiong M, Jin L, 2018
Identification and Functional Studies of MYO1H for Mandibular Prognathism, Sun R, Wang Y, Jin M, Chen L, Cao Y, Chen F, 2018
A study on fast calling variants from next-generation sequencing data using decision tree, Li Z, Wang Y, Wang F, 2018
A standardized fold change method for microarray differential expression analysis used to reveal genes involved in acute rejection in murine allograft models, Zhou W, Wang Y, Fujino M, Shi L, Jin L, Li XK, Wang J, 2018
Bagging Nearest-Neighbor Prediction independence Test: an efficient method for nonlinear dependence of two continuous variables, Wang Y, Li Y, Liu X, Pu W, Wang X, Wang J, Xiong M, Yao Shugart Y, Jin L, 2017
Fine population structure analysis method for genomes of many, Pan X, Wang Y, Wong EHM, Telenti A, Venter JC, Jin L, 2017
Genome-wide screening for highly discriminative SNPs for personal identification and their assessment in world populations, Li L, Wang Y, Yang S, Xia M, Yang Y, Wang J, Lu D, Pan X, Ma T, Jiang P, Yu G, Zhao Z, Ping Y, Zhou H, Zhao X, Sun H, Liu B, Jia D, Li C, Hu R, Lu H, Liu X, Chen W, Mi Q, Xue F, Su Y, Jin L, Li S, 2017
SeqCNV: a novel method for identification of copy number variations in targeted next-generation sequencing data, Chen Y, Zhao L, Wang Y, Cao M, Gelowani V, Xu M, Agrawal SA, Li Y, Daiger SP, Gibbs R, Wang F, Chen R, 2017
A fast read alignment method based on seed-and-vote for next generation sequencing, Liu S, Wang Y, Wang F, 2016
Random Bits Forest: a Strong Classifier/Regressor for Big Data, Wang Y, Li Y, Pu W, Wen K, Shugart YY, Xiong M, Jin L, 2016
Random Bits Regression: a Strong General Predictor for Big Data, Yi Wang, Yi Li, Momiao Xiong, Yin Yao Shugart, Li Jin, 2016
Efficient test for nonlinear dependence of two continuous variables, Wang Y, Y. Li, H. Cao, M. Xiong, Y. Y. Shugart, L. Jin, 2015
An integrative variant analysis pipeline for accurate genotype/haplotype inference in population NGS data, Wang Y, Lu J, Yu J, Gibbs RA, Yu F, 2013
An integrated map of genetic variation from 1,092 human genomes, Abecasis, G. R., A. Auton, L. D. Brooks, M. A. DePristo, R. M. Durbin, R. E. Handsaker, H. M. Kang, G. T. Marth, G. A. McVean, 2012
Novel statistical framework to identify differentially expressed genes allowing transcriptomic background differences, Ling ZQ, Wang Y, Mukaisho K, Hattori T, Tatsuta T, Ge MH, Jin L, Mao WM, Sugihara H, 2010
