Guosheng Zhang

发表

FastHiC: a fast and accurate algorithm to detect long-range chromosomal interactions from Hi-C data

Yun Li, Ming Hu, Zheng Xu, 2016, Bioinform..

A hidden Markov random field-based Bayesian method for the detection of long-range chromosomal interactions in Hi-C data

Terrence S. Furey, Zheng Xu, Yun Li, 2016, Bioinform..

Imputation of coding variants in African Americans: better performance using data from the exome sequencing project

Jennifer G. Robinson, C. Carlson, T. Assimes, 2013, Bioinform..

Across‐Platform Imputation of DNA Methylation Levels Incorporating Nonlocal Information Using Penalized Functional Regression

Jung-Ying Tzeng, Yun Li, Weihua Guan, 2016, Genetic epidemiology.

Imputation of exome sequence variants into population- based samples and blood-cell-trait-associated loci in African Americans: NHLBI GO Exome Sequencing Project.

Benjamin A. Logsdon, Andrew D. Johnson, M. Nalls, 2012, American journal of human genetics.

Blood Leukocyte DNA Methylation Predicts Risk of Future Myocardial Infarction and Coronary Heart Disease.

S. Horvath, Brian H Chen, E. Colicino, 2019, Circulation.

DNA Methylation Analysis Identifies Loci for Blood Pressure Regulation.

May E. Montasser, Min A. Jhun, S. Horvath, 2017, American journal of human genetics.

DNA Methylation Signatures of Depressive Symptoms in Middle-aged and Elderly Persons: Meta-analysis of Multiethnic Epigenome-wide Studies

R. Marioni, J. Bressler, M. Fornage, 2018, JAMA psychiatry.

A longitudinal study of DNA methylation as a potential mediator of age-related diabetes risk

L. Hou, J. Manson, A. Baccarelli, 2017, GeroScience.

Combined Targeted DNA Sequencing in Non-Small Cell Lung Cancer (NSCLC) Using UNCseq and NGScopy, and RNA Sequencing Using UNCqeR for the Detection of Genetic Aberrations in NSCLC

D. Hayes, M. Wilkerson, M. Gulley, 2015, PloS one.

Relatively Small Contribution of Methylation and Genomic Copy Number Aberration to the Aberrant Expression of Inflammation-Related Genes in HBV-Related Hepatocellular Carcinoma

Yun Li, W. Tan, Chen Wu, 2015, PloS one.

HiView: an integrative genome browser to leverage Hi-C results for the interpretation of GWAS variants

Baqun Zhang, Feng Yue, Yun Li, 2016, BMC Research Notes.

One Size Doesn't Fit All - RefEditor: Building Personalized Diploid Reference Genome to Improve Read Mapping and Genotype Calling in Next Generation Sequencing Studies

Yun Li, Shuai Yuan, Guosheng Zhang, 2015, PLoS Comput. Biol..