The following pages link to Biostatistics (Q63386):
Displaying 50 items.
- Hypothesis testing for neural cell growth experiments using a hybrid branching process model (Q3303628) (← links)
- HIV with contact tracing: a case study in approximate Bayesian computation (Q3303629) (← links)
- On inferring presence of an individual in a mixture: a Bayesian approach (Q3303630) (← links)
- Testing and interval estimation for two-sample survival comparisons with small sample sizes and unequal censoring (Q3303631) (← links)
- Cox regression model with time-varying coefficients in nested case-control studies (Q3303632) (← links)
- Calibrating disease progression models using population data: a critical precursor to policy development in cancer control (Q3303634) (← links)
- Spatial misalignment in time series studies of air pollution and health data (Q3303635) (← links)
- Sequential predictions of menstrual cycle lengths (Q3303636) (← links)
- Identification of causal effects on binary outcomes using structural mean models (Q3303637) (← links)
- Testing for misspecification in generalized linear mixed models (Q3303638) (← links)
- Methods for testing association between uncertain genotypes and quantitative traits (Q3303643) (← links)
- Testing SNPs and sets of SNPs for importance in association studies (Q3303644) (← links)
- A multilevel model to address batch effects in copy number estimation using SNP arrays (Q3303648) (← links)
- Multiple testing on standardized mortality ratios: a Bayesian hierarchical model for FDR estimation (Q3303649) (← links)
- Adaptive index models for marker-based risk stratification (Q3303650) (← links)
- Estimating the diagnostic likelihood ratio of a continuous marker (Q3303652) (← links)
- A multistate model for events defined by prolonged observation (Q3303653) (← links)
- Doubly robust estimation of attributable fractions (Q3303654) (← links)
- Two-dimensional toxic dose and multivariate logistic regression, with application to decompression sickness (Q3303655) (← links)
- Feature selection in finite mixture of sparse normal linear models in high-dimensional feature space (Q3303656) (← links)
- A composite likelihood approach to the analysis of longitudinal clonal data on multitype cellular systems under an age-dependent branching process (Q3303657) (← links)
- Accurate genome-scale percentage DNA methylation estimates from microarray data (Q3303662) (← links)
- Bayesian epistasis association mapping via SNP imputation (Q3303663) (← links)
- Estimation and selection in high-dimensional genomic studies for developing molecular diagnostics (Q3303664) (← links)
- Clustering with exclusion zones: genomic applications (Q3303666) (← links)
- A structural mean model to allow for noncompliance in a randomized trial comparing 2 active treatments (Q3303668) (← links)
- Inference on treatment effects from a randomized clinical trial in the presence of premature treatment discontinuation: the SYNERGY trial (Q3303671) (← links)
- Analysis of randomized comparative clinical trial data for personalized treatment selections (Q3303673) (← links)
- Model structure analysis to estimate basic immunological processes and maternal risk for parvovirus B19 (Q3303674) (← links)
- Joint estimation of the basic reproduction number and generation time parameters for infectious disease outbreaks (Q3303677) (← links)
- Methods for clustered encouragement design studies with noncompliance and missing data (Q3303679) (← links)
- Constrained inference in mixed-effects models for longitudinal data with application to hearing loss (Q3303681) (← links)
- Functional mixture regression (Q3303682) (← links)
- Estimation of the 2-sample hazard ratio function using a semiparametric model (Q3303683) (← links)
- Marker selection via maximizing the partial area under the ROC curve of linear risk scores (Q3303684) (← links)
- Continual reassessment method with multiple toxicity constraints (Q3303685) (← links)
- Learning from our GWAS mistakes: from experimental design to scientific method (Q3303807) (← links)
- Removing technical variability in RNA-seq data using conditional quantile normalization (Q3303808) (← links)
- Sample size determination for classifiers based on single-nucleotide polymorphisms (Q3303809) (← links)
- Family-based association tests using genotype data with uncertainty (Q3303810) (← links)
- Classification method for disease risk mapping based on discrete hidden Markov random fields (Q3303812) (← links)
- On the covariate-adjusted estimation for an overall treatment difference with data from a randomized comparative clinical trial (Q3303813) (← links)
- A two-stage strategy to accommodate general patterns of confounding in the design of observational studies (Q3303814) (← links)
- Estimating causal effects of air quality regulations using principal stratification for spatially correlated multivariate intermediate outcomes (Q3303815) (← links)
- A measure of explained risk in the proportional hazards model (Q3303816) (← links)
- Robust best linear estimation for regression analysis using surrogate and instrumental variables (Q3303817) (← links)
- A Bayesian model for time-to-event data with informative censoring (Q3303820) (← links)
- A marginalized conditional linear model for longitudinal binary data when informative dropout occurs in continuous time (Q3303821) (← links)
- Effective communication of standard errors and confidence intervals (Q3304903) (← links)
- Case series analysis for censored, perturbed, or curtailed post-event exposures (Q3304904) (← links)
