Note: The ones
with * list me as the corresponding/co-corresponding author.
Nonparametric Bayesian Methods and Applications in
Statistical Genetics and Bioinformatics
1. Dunson, D. B. and Xing, C. (2009). Bayesian nonparametric
modeling of multi-variate unordered categorical data. Journal
of the American Statistical Association 104, 1042-1051.
2. Xing, C.* and Dunson, D. B. (2011). Bayesian inference
for genomic data integration reduces misclassification rate in predicting
protein-protein interactions. PLoS Computational Biology
7(7), e1002110. PMID: 21829334 (reported online by GenomeWeb).
3. Xing, C.*, Kunihama, T. Kiel, D. P., Cupples, L. A., and Dunson,
D. B. Genetic interaction networks for integrative identification
of disease risks in signal pathways using a nonparametric Bayes model.
American Journal of Human Genetics (to be submitted, manuscript
available upon request).
4. Xing, C.*, Yang, Q., Allen, A. S., and Li, Y-J. Genetic
association using Bayesian modeling for the family based and inrelated
case-control data (to be submitted).
5. Xing, C.* et al. Kiel, D. P. Fat intake by gene interactions
on quantitative computed tomography derived bone density (to be
submitted).
Semi-Parametric Modeling, Multivariate Analysis and
Regression Modeling in Statistical Genetics
6. Xing, C.*, Dupuis, J., Cupples, L. A. Meigs, J. B., Lin, X,
and Allen, A. S. A robust approach for analyzing secondary phenotypes
in case-control genetic association studies. American Journal
of Human Genetics (submitted, manuscript available upon request).
7. Guo, W., Yang, M., Xing, C., and Peddada, S. D. (2012).
Analysis of high dimensional data using predefined set and subset information,
with applications to genomic data. BMC Bioinformatics
13, 177 (highly accessed).
8. Xing, C.*, Satten, G. A., and Allen, A. S. (2011). A weighted
accumulation test for associating rare genetic variation with quantitative
phenotypes. BMC Proceedings 5(Suppl 9), S6,doi:10.1186/1753-6561-5-S9-S6.
9. Xing, C., Huang, J. Hsu, Y-H, Destefano, A. L., Heard-Costa,
N. L., Wolf, P. A., Seshadri, S., Kiel, D. P. Cupples, L. A., and Dupuis,
J. Evaluation of Power of the Illumina HumanOmni5M-4v1 BeadChip to
Detect Susceptible Variants for Human Complex Diseases. American
Journal of Human Genetics (submitted, manuscript available upon
request).
10. Xing, C.*, Dupuis, J., and Cupples, L. A. Performance
of Statistical Methods on CHARGE-S Targeted Sequencing Data. Genetic
Epidemiology (submitted, manuscript available upon request).
11. Lin H. H., Wang, M., Brody, J. A., BA, Bis, J. C.,
, Xing,
C.,
, Cupples, L. A., Bressler, J., Boerwinkle, E. Strategies
to Design and Analyze Targeted Sequencing Data: the Cohorts for Heart
and Aging Research in Genomic Epidemiology (CHARGE) Targeted Sequencing
Study (submitted).
Time Series/Signal Processing in Genomics
12. Xing, C.*, Bitzer, D. L., and Alexander, W. E., Vouk, M.
A., and Stomp A-M. (2009). Identification of protein-coding sequences
using the hybridization of 18S rRNA and mRNA during translation.
Nucleic Acids Research 37(2), 591-601.
Conference Publications
13. Xing, C.*, Bitzer, D. L., Alexander, W. E. and Stomp, A-M.
(2007). Thermodynamics exploration to identify donor sites for yeast.
Proceedings of the IEEE International Workshop on Genomic Signal Processing
& Statistics 65-66.
14. Xing, C.*, Bitzer D. L., Alexander, W. E., Stomp, A. M.,
Vouk, M. A. (2006). Free energy analysis on the coding region of
the individual genes of Saccharomyces cerevisiae. Proceeding
of the IEEE Engineering Medicine and Biology Society. 2006; 4225-4228.
15. Xing, C.*, Mishra, M., Vu, S. K., Alexander, W. E., Bitzer,
D. L., and Vouk, M. A. (2004). Free energy based analysis of the
coding region of Saccharomyces cerevisiae. Technology for Life:
North Carolina Symposium on Biotechnology and Bioinformatics 25-27.
16. Xing, C.*, Bitzer, D. L., Alexander, W. E., and Stomp, A-M.
(2005). Splicing Sites Identification by Thermodynamic modelling
algorithm and analytical method in Saccharomyces Cerevisiae. The
North Carolina RNA Society Symposium on RNA Biology (Abstract).
17. Whelan, S. A., Theberge, R., Spencer, J. L., Griffin, P., Xing,
C., Steinberg, M. H., Costello, C. E., Klings, E. S., Mccomb, M.
E. (2013). Protein and Post-Translational Modification Markers in
Sickle Cell Disease. 61st ASMS Conference on Mass Spectrometry
and Allied Topics.
18. Leymarie, N., Griffin, P., Xing, C., Jonscher, K., Kolarich,
D., Orlando, R., Mccomb, M., Zaia, J. (2013). Ability of the glycoproteomics
comminuty to profile N-glycosylation of prostate specific antigen by
mass spectrometry: an ABRF 2013 Interlaboratory Study. 61st ASMS
Conference on Mass Spectrometry and Allied Topics.
Book Chapters
19. Chuanhua Xing. Methods of Molecular Biology Series: Methods
to predict translated pseudogenes: hybridization of 18S rRNA and mRNA
during translation. Humana Press (www.springer.com/humana), 2013
(in press).
Dissertation
20. Chuanhua Xing. (2007). Analysis and Identification of Protein-coding
Sequences for Yeast Using Signal Processing Approaches
Working Papers
21. Xing, C.* Allen, A. S, and Lin, X. Secondary phenotypes
in sequencing case-control genetic association studies considering gene-secondary
phenotype interaction.
22. Hua, Z, Hu, M., and Xing, C. Bayesian Biomarker Integrative
Inference in Response Prediction.
23. Xing, C.*, Lin, H., Kunihama, T. and Dunson, D. B., and Lunneta,
K. Functional SNP set analysis in atrial fibrillation.
24. Xing, C.* and Shi, M. A conserved sequence and identity
by descent mapping based model to identifying rare disease-risk variants
avoids large sample size and low power.
25. Xing, C.*, Griffin, P., and Klings, E. S. Joint analysis
of Microarray data with phenotype-genotype data for elevated tricuspid
regurgitant jet velocity in sickle cell disease.