The following pages link to Shili Lin (Q906227):
Displaying 31 items.
- \texttt{TopKLists}: a comprehensive \texttt{R} package for statistical inference, stochastic aggregation, and visualization of multiple omics ranked lists (Q906228) (← links)
- A robust unified approach to analyzing methylation and gene expression data (Q961331) (← links)
- Using the partitioning principle to construct confidence sets for the location of a disease gene (Q1888886) (← links)
- Robust partial likelihood approach for detecting imprinting and maternal effects using case-control families (Q1951529) (← links)
- Monte Carlo Bayesian methods for quantitative traits (Q1960473) (← links)
- Examining the rare disease assumption used to justify HWE testing with control samples (Q2045652) (← links)
- AIJ: joint test for simultaneous detection of imprinting and non-imprinting allelic expression imbalance (Q2045691) (← links)
- Mixture modeling of progression pathways of heterogeneous breast tumors (Q2216298) (← links)
- Space oriented rank-based data integration (Q2254455) (← links)
- A Bayesian mixture model for chromatin interaction data (Q2258449) (← links)
- A mixture modeling framework for differential analysis of high-throughput data (Q2262632) (← links)
- Capturing heterogeneity of covariate effects in hidden subpopulations in the presence of censoring and large number of covariates (Q2415472) (← links)
- Optimum study design for detecting imprinting and maternal effects based on partial likelihood (Q2805185) (← links)
- Statistical Inference on Three-Dimensional Structure of Genome by Truncated Poisson Architecture Model (Q2806340) (← links)
- Regularization in Finite Mixture of Regression Models with Diverging Number of Parameters (Q2846451) (← links)
- Likelihood Approach for Detecting Imprinting and In Utero Maternal Effects Using General Pedigrees from Prospective Family-Based Association Studies (Q2912343) (← links)
- Logistic Bayesian LASSO for Identifying Association with Rare Haplotypes and Application to Age-Related Macular Degeneration (Q2912358) (← links)
- Information Gain for Genetic Parameter Estimation with Incorporation of Marker Data (Q3079127) (← links)
- Feature selection in finite mixture of sparse normal linear models in high-dimensional feature space (Q3303656) (← links)
- A Bayesian Approach for Incorporating Variable Rates of Heterogeneity in Linkage Analysis (Q3434197) (← links)
- Integration of Ranked Lists via Cross Entropy Monte Carlo with Applications to mRNA and microRNA Studies (Q3623735) (← links)
- (Q4203529) (← links)
- Multipoint Linkage Analysis via Metropolis Jumping Kernels (Q4335598) (← links)
- A Scheme for Constructing an Irreducible Markov Chain for Pedigree Data (Q4844329) (← links)
- Imprinting and Maternal Effect Detection Using Partial Likelihood Based on Discordant Sibpair Data (Q5243742) (← links)
- A random effect model for reconstruction of spatial chromatin structure (Q5347402) (← links)
- Detecting rare and common haplotype–environment interaction under uncertainty of gene–environment independence assumption (Q5347448) (← links)
- Modeling and Analysis of Multi‐Library, Multi‐Group SAGE Data with Application to a Study of Mouse Cerebellum (Q5434907) (← links)
- (Q5686993) (← links)
- Bayesian LASSO for population stratification correction in rare haplotype association studies (Q6544874) (← links)
- Sparse estimation in semiparametric finite mixture of varying coefficient regression models (Q6589289) (← links)