Pages that link to "Item:Q77768"
From MaRDI portal
The following pages link to Statistical Applications in Genetics and Molecular Biology (Q77768):
Displaying 50 items.
- Meta-analysis of family-based and case-control genetic association studies that use the same cases (Q458228) (← links)
- Deviance information criteria for model selection in approximate Bayesian computation (Q458231) (← links)
- Assessing modularity using a random matrix theory approach (Q458235) (← links)
- A three component latent class model for robust semiparametric gene discovery (Q458238) (← links)
- Inferring gene networks using robust statistical techniques (Q458242) (← links)
- On the statistical properties of SGoF multitesting method (Q458244) (← links)
- Fully moderated \(t\)-statistic for small sample size gene expression arrays (Q458251) (← links)
- A two-stage Poisson model for testing RNA-Seq data (Q458254) (← links)
- Interval estimation of familial correlations from pedigrees (Q458258) (← links)
- Imputation estimators partially correct for model misspecification (Q458262) (← links)
- Comparison of clinical subgroup aCGH profiles through pseudolikelihood ratio tests (Q458267) (← links)
- Large sample approximations of probabilities of correct evolutionary tree estimation and biases of maximum likelihood estimation (Q458269) (← links)
- Repeated measures semiparametric regression using targeted maximum likelihood methodology with application to transcription factor activity discovery (Q458271) (← links)
- Sparse canonical covariance analysis for high-throughput data (Q458273) (← links)
- Analyzing time-course microarray data using functional data analysis -- a review (Q458276) (← links)
- Fast identification of biological pathways associated with a quantitative trait using group lasso with overlaps (Q458798) (← links)
- Stopping-time resampling and population genetic inference under coalescent models (Q458799) (← links)
- Alignment-free sequence comparison for biologically realistic sequences of moderate length (Q458802) (← links)
- A mixture-model approach for parallel testing for unequal variances (Q458805) (← links)
- Improving hidden Markov models for classification of human immunodeficiency virus-1 subtypes through linear classifier learning (Q458808) (← links)
- A model-based analysis to infer the functional content of a gene list (Q458812) (← links)
- A generalized hidden Markov model for determining sequence-based predictors of nucleosome positioning (Q458815) (← links)
- A family-based probabilistic method for capturing de novo mutations from high-throughput short-read sequencing data (Q458820) (← links)
- Adjusting for spurious gene-by-environment interaction using case-parent triads (Q458823) (← links)
- Querying genomic databases: refining the connectivity map (Q458827) (← links)
- Principal components of heritability for high dimension quantitative traits and general pedigrees (Q458833) (← links)
- Bayesian sparsity-path-analysis of genetic association signal using generalized \(t\) priors (Q458836) (← links)
- Hierarchical Bayes model for predicting effectiveness of HIV combination therapies (Q458839) (← links)
- Exploring multicollinearity using a random matrix theory approach (Q458840) (← links)
- Empirical Bayes interval estimates that are conditionally equal to unadjusted confidence intervals or to default prior credibility intervals (Q458841) (← links)
- Borrowing information across genes and experiments for improved error variance estimation in microarray data analysis (Q458842) (← links)
- Detection of differentially expressed gene sets in a partially paired microarray data set (Q458845) (← links)
- Testing clonality of three and more tumors using their loss of heterozygosity profiles (Q461626) (← links)
- Hessian calculation for phylogenetic likelihood based on the pruning algorithm and its applications (Q461628) (← links)
- An integrated hierarchical Bayesian model for multivariate eQTL mapping (Q461634) (← links)
- A Bayesian autoregressive three-state hidden Markov model for identifying switching monotonic regimes in microarray time course data (Q461635) (← links)
- Performance of MAX test and degree of dominance index in predicting the mode of inheritance (Q461637) (← links)
- Estimating the number of one-step beneficial mutations (Q461640) (← links)
- Cluster-localized sparse logistic regression for SNP data (Q461649) (← links)
- Incorporating genomic annotation into a hidden Markov model for DNA methylation tiling array data (Q461652) (← links)
- ExactDAS: an exact test procedure for the detection of differential alternative splicing in microarray experiments (Q461656) (← links)
- Genotype copy number variations using Gaussian mixture models: theory and algorithms (Q461658) (← links)
- DNA pooling and statistical tests for the detection of single nucleotide polymorphisms (Q461660) (← links)
- Large-scale parentage inference with SNPs: an efficient algorithm for statistical confidence of parent pair allocations (Q461662) (← links)
- A PAUC-based estimation technique for disease classification and biomarker selection (Q461666) (← links)
- An order estimation based approach to identify response genes for microarray time course data (Q461669) (← links)
- Hierarchical shrinkage priors and model fitting for high-dimensional generalized linear models (Q461671) (← links)
- Statistical inference of regulatory networks for circadian regulation (Q461673) (← links)
- A Bayesian clustering approach for detecting gene-gene interactions in high-dimensional genotype data (Q461676) (← links)
- A novel characterization of the generalized family wise error rate using empirical null distributions (Q461678) (← links)