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In comparative high-throughput sequencing assays, a fundamental task is the analysis of count data, such as read counts per gene in RNA-seq, for evidence of systematic changes across experimental conditions. Small replicate numbers, discreteness, large dynamic range and the presence of outliers require a suitable statistical approach. We present DESeq2, a method for differential analysis of count data, using shrinkage estimation for dispersions and fold changes to improve stability and interpretability of estimates. This enables a more quantitative analysis focused on the strength rather than the mere presence of differential expression. The DESeq2 package is available at http://www.bioconductor.org/packages/release/bioc/html/DESeq2.html webcite.
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Love et al. (Fri,) studied this question.
www.synapsesocial.com/papers/69bd604c331c354bb52ff529 — DOI: https://doi.org/10.1186/s13059-014-0550-8
Michael I. Love
Wolfgang Huber
Simon Anders
Genome biology
Dana-Farber Cancer Institute
European Molecular Biology Laboratory
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