Підписатись
Can Yang
Назва
Посилання
Посилання
Рік
Moving object detection by detecting contiguous outliers in the low-rank representation
X Zhou, C Yang, W Yu
IEEE transactions on pattern analysis and machine intelligence 35 (3), 597-610, 2012
7782012
BOOST: A fast approach to detecting gene-gene interactions in genome-wide case-control studies
X Wan, C Yang, Q Yang, H Xue, X Fan, NLS Tang, W Yu
The American Journal of Human Genetics 87 (3), 325-340, 2010
6102010
GPA: a statistical approach to prioritizing GWAS results by integrating pleiotropy and annotation
D Chung, C Yang, C Li, J Gelernter, H Zhao
PLoS genetics 10 (11), e1004787, 2014
2282014
SNPHarvester: a filtering-based approach for detecting epistatic interactions in genome-wide association studies
C Yang, Z He, X Wan, Q Yang, H Xue, W Yu
Bioinformatics 25 (4), 504-511, 2009
2072009
Predictive rule inference for epistatic interaction detection in genome-wide association studies
X Wan, C Yang, Q Yang, H Xue, NLS Tang, W Yu
Bioinformatics 26 (1), 30-37, 2010
2032010
Genome-wide association study identifies new susceptibility loci for posttraumatic stress disorder
P Xie, HR Kranzler, C Yang, H Zhao, LA Farrer, J Gelernter
Biological psychiatry 74 (9), 656-663, 2013
1982013
GBOOST: a GPU-based tool for detecting gene–gene interactions in genome–wide case control studies
LS Yung, C Yang, X Wan, W Yu
Bioinformatics 27 (9), 1309-1310, 2011
1982011
Low-rank modeling and its applications in image analysis
X Zhou, C Yang, H Zhao, W Yu
ACM Computing Surveys (CSUR) 47 (2), 1-33, 2014
1942014
Total variation regularized tensor RPCA for background subtraction from compressive measurements
W Cao, Y Wang, J Sun, D Meng, C Yang, A Cichocki, Z Xu
IEEE Transactions on Image Processing 25 (9), 4075-4090, 2016
1852016
Bayesian weighted Mendelian randomization for causal inference based on summary statistics
J Zhao, J Ming, X Hu, G Chen, J Liu, C Yang
Bioinformatics 36 (5), 1501-1508, 2020
1812020
Leveraging functional annotations in genetic risk prediction for human complex diseases
Y Hu, Q Lu, R Powles, X Yao, C Yang, F Fang, X Xu, H Zhao
PLoS computational biology 13 (6), e1005589, 2017
1772017
An international effort towards developing standards for best practices in analysis, interpretation and reporting of clinical genome sequencing results in the CLARITY Challenge
CA Brownstein, AH Beggs, N Homer, B Merriman, TW Yu, KC Flannery, ...
Genome biology 15, 1-18, 2014
1272014
Testing and controlling for horizontal pleiotropy with probabilistic Mendelian randomization in transcriptome-wide association studies
Z Yuan, H Zhu, P Zeng, S Yang, S Sun, C Yang, J Liu, X Zhou
Nature communications 11 (1), 3861, 2020
1262020
Deep generative learning via schrödinger bridge
G Wang, Y Jiao, Q Xu, Y Wang, C Yang
International conference on machine learning, 10794-10804, 2021
1152021
A unified framework for cross-population trait prediction by leveraging the genetic correlation of polygenic traits
M Cai, J Xiao, S Zhang, X Wan, H Zhao, G Chen, C Yang
The American Journal of Human Genetics 108 (4), 632-655, 2021
1002021
Pervasive pleiotropy between psychiatric disorders and immune disorders revealed by integrative analysis of multiple GWAS
Q Wang, C Yang, J Gelernter, H Zhao
Human genetics 134, 1195-1209, 2015
962015
MegaSNPHunter: a learning approach to detect disease predisposition SNPs and high level interactions in genome wide association study
X Wan, C Yang, Q Yang, H Xue, NLS Tang, W Yu
BMC bioinformatics 10, 1-15, 2009
952009
Comments on 'An empirical comparison of several recent epistatic interaction detection methods'.
X Wan, C Yang, W Yu
Bioinformatics, 2011
882011
Improving genetic risk prediction by leveraging pleiotropy
C Li, C Yang, J Gelernter, H Zhao
Human genetics 133, 639-650, 2014
872014
On high-dimensional misspecified mixed model analysis in genome-wide association study
J Jiang, C Li, D Paul, C Yang, H Zhao
782016
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Статті 1–20