Areas of Focus
- 医学遗传学
- 生物信息
- 医学人工智能
Work Experience
- 2010.4-2011.8：美国贝勒医学院人类基因组测序中心，博士后
- 2012.8-2016.7：复旦大学现代人类学教育部重点实验室，助理研究员
- 2016.8-今：复旦大学生命科学学院，青年副研究员
Academic Background & Achievements
- 2000.9-2004.7：复旦大学生命科学学院，学士
- 2004.9-2009.12：复旦大学现代人类学教育部重点实验室，遗传学博士
Publications
- 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
