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Open AccessJournal ArticleDOI

voom: precision weights unlock linear model analysis tools for RNA-seq read counts

TLDR
New normal linear modeling strategies are presented for analyzing read counts from RNA-seq experiments, and the voom method estimates the mean-variance relationship of the log-counts, generates a precision weight for each observation and enters these into the limma empirical Bayes analysis pipeline.
Abstract
New normal linear modeling strategies are presented for analyzing read counts from RNA-seq experiments. The voom method estimates the mean-variance relationship of the log-counts, generates a precision weight for each observation and enters these into the limma empirical Bayes analysis pipeline. This opens access for RNA-seq analysts to a large body of methodology developed for microarrays. Simulation studies show that voom performs as well or better than count-based RNA-seq methods even when the data are generated according to the assumptions of the earlier methods. Two case studies illustrate the use of linear modeling and gene set testing methods.

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The START App: a web-based RNAseq analysis and visualization resource

TL;DR: The START (Shiny Transcriptome Analysis Resource Tool) App has the power and flexibility to be resident on a local computer or serve as a web‐based environment, enabling easy sharing of data between researchers and collaborators.
Journal ArticleDOI

Comparison of methods to detect differentially expressed genes between single-cell populations

TL;DR: This work compared five statistical methods to detect differentially expressed genes between two distinct single-cell populations and found the previously introduced reproducibility-optimization method showed good performance in all comparison settings without any single- cell-specific modifications.
Journal ArticleDOI

Genetic dissection of the miR-200–Zeb1 axis reveals its importance in tumor differentiation and invasion

TL;DR: It is shown that miR-200 ablation in the Rip-Tag2 insulinoma mouse model induces beta-cell dedifferentiation, EMT and tumor invasion, and that disruption of Zeb1 regulation by miR -200c is sufficient to drive EMT.
Journal ArticleDOI

Analytical tools and current challenges in the modern era of neuroepigenomics

TL;DR: A comprehensive overview of available tools for analyzing neuroepigenomics data is provided, as well as a discussion of pending challenges specific to the field of neuroscience.
References
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Journal ArticleDOI

edgeR: a Bioconductor package for differential expression analysis of digital gene expression data.

TL;DR: EdgeR as mentioned in this paper is a Bioconductor software package for examining differential expression of replicated count data, which uses an overdispersed Poisson model to account for both biological and technical variability and empirical Bayes methods are used to moderate the degree of overdispersion across transcripts, improving the reliability of inference.
Book

Generalized Linear Models

TL;DR: In this paper, a generalization of the analysis of variance is given for these models using log- likelihoods, illustrated by examples relating to four distributions; the Normal, Binomial (probit analysis, etc.), Poisson (contingency tables), and gamma (variance components).
Journal ArticleDOI

featureCounts: an efficient general-purpose program for assigning sequence reads to genomic features

TL;DR: FeatureCounts as discussed by the authors is a read summarization program suitable for counting reads generated from either RNA or genomic DNA sequencing experiments, which implements highly efficient chromosome hashing and feature blocking techniques.
Journal ArticleDOI

Differential expression analysis for sequence count data.

Simon Anders, +1 more
- 27 Oct 2010 - 
TL;DR: A method based on the negative binomial distribution, with variance and mean linked by local regression, is proposed and an implementation, DESeq, as an R/Bioconductor package is presented.
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