The following pages link to edgeR (Q19000):
Displaying 50 items.
- Modeling microbial abundances and dysbiosis with beta-binomial regression (Q86089) (← links)
- Statistical genomics. Methods and protocols (Q293809) (← links)
- A Markov random field-based approach for joint estimation of differentially expressed genes in mouse transcriptome data (Q306683) (← links)
- Shrinkage of dispersion parameters in the binomial family, with application to differential exon skipping (Q312910) (← links)
- Robust hyperparameter estimation protects against hypervariable genes and improves power to detect differential expression (Q312950) (← links)
- Modeling read counts for CNV detection in exome sequencing data (Q458185) (← links)
- Comparing segmentation methods for genome annotation based on RNA-seq data (Q486163) (← links)
- Estimation and testing of gene expression heterosis (Q489924) (← links)
- Anesthetic propofol-induced gene expression changes in patients undergoing coronary artery bypass graft surgery based on dynamical differential coexpression network analysis (Q519629) (← links)
- A simulation framework for correlated count data of features subsets in high-throughput sequencing or proteomics experiments (Q521444) (← links)
- Controlling the false-discovery rate by procedures adapted to the length bias of RNA-seq (Q684055) (← links)
- HmmSeq: a hidden Markov model for detecting differentially expressed genes from RNA-seq data (Q746680) (← links)
- Classification and clustering of sequencing data using a Poisson model (Q765993) (← links)
- Hierarchical modeling and differential expression analysis for RNA-seq experiments with inbred and hybrid genotypes (Q906080) (← links)
- Empirical Bayes analysis of RNA-seq data for detection of gene expression heterosis (Q906083) (← links)
- Nonparametric Bayesian learning of heterogeneous dynamic transcription factor networks (Q1621019) (← links)
- Statistical analysis of microbiome data with R (Q1622658) (← links)
- Bayesian analysis of RNA-Seq data using a family of negative binomial models (Q1631554) (← links)
- Modifying SAMseq to account for asymmetry in the distribution of effect sizes when identifying differentially expressed genes (Q1670284) (← links)
- Bayesian estimation of differential transcript usage from RNA-seq data (Q1670291) (← links)
- Bioinformatics. Volume II: structure, function, and applications (Q1691857) (← links)
- MATHT: a web server for comprehensive transcriptome data analysis (Q1714286) (← links)
- Computational cell biology. Methods and protocols (Q1721982) (← links)
- On computing maximum likelihood estimates for the negative binomial distribution (Q1726917) (← links)
- A statistical perspective on the challenges in molecular microbial biology (Q2084409) (← links)
- A sparse negative binomial classifier with covariate adjustment for RNA-seq data (Q2154214) (← links)
- Contrastive latent variable modeling with application to case-control sequencing experiments (Q2170381) (← links)
- Structured hierarchical models for probabilistic inference from perturbation screening data (Q2170453) (← links)
- Bayesian mixed effects models for zero-inflated compositions in microbiome data analysis (Q2179984) (← links)
- A novel individualized drug repositioning approach for predicting personalized candidate drugs for type 1 diabetes mellitus (Q2195265) (← links)
- Identifying atypically expressed chromosome regions using RNA-Seq data (Q2220294) (← links)
- Bayesian sparse multivariate regression with asymmetric nonlocal priors for microbiome data analysis (Q2226696) (← links)
- Model-based feature selection and clustering of RNA-seq data for unsupervised subtype discovery (Q2233190) (← links)
- An empirical Bayes change-point model for transcriptome time-course data (Q2233191) (← links)
- Statistical analysis of next generation sequencing data (Q2250275) (← links)
- A Bayesian mixture model for chromatin interaction data (Q2258449) (← links)
- RNA bioinformatics (Q2259130) (← links)
- Nonparametric false discovery rate control for identifying simultaneous signals (Q2286361) (← links)
- Modeling association in microbial communities with clique loglinear models (Q2318667) (← links)
- General power and sample size calculations for high-dimensional genomic data (Q2344242) (← links)
- No counts, no variance: allowing for loss of degrees of freedom when assessing biological variability from RNA-seq data (Q2406178) (← links)
- Random forests in count data modelling: an analysis of the influence of data features and overdispersion on regression performance (Q2684565) (← links)
- Pathway analysis for RNA-Seq data using a score-based approach (Q2805192) (← links)
- Modeling overdispersion heterogeneity in differential expression analysis using mixtures (Q2827191) (← links)
- Bioinformatics for High Throughput Sequencing (Q3191914) (← links)
- Removing technical variability in RNA-seq data using conditional quantile normalization (Q3303808) (← links)
- BNP-Seq: Bayesian Nonparametric Differential Expression Analysis of Sequencing Count Data (Q4690929) (← links)
- A semi-parametric Bayesian approach for detection of gene expression heterosis with RNA-seq data (Q5058236) (← links)
- Poisson–Tweedie mixed-effects model: A flexible approach for the analysis of longitudinal RNA-seq data (Q5070489) (← links)
- Computational Genomics with R (Q5151092) (← links)
