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samExploreR: exploring reproducibility and robustness of RNA-seq results based on SAM files

Data from RNA-seq experiments provide us with many new possibilities to gain insights into biological and disease mechanisms of cellular functioning. However, the reproducibility and robustness of RNA-seq data analysis results is often unclear. This is in part attributed to the two counter acting go...

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Bibliographic Details
Published in:Bioinformatics (Oxford, England) England), 2016-11, Vol.32 (21), p.3345-3347
Main Authors: Stupnikov, Alexey, Tripathi, Shailesh, de Matos Simoes, Ricardo, McArt, Darragh, Salto-Tellez, Manuel, Glazko, Galina, Dehmer, Matthias, Emmert-Streib, Frank
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Language:English
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Summary:Data from RNA-seq experiments provide us with many new possibilities to gain insights into biological and disease mechanisms of cellular functioning. However, the reproducibility and robustness of RNA-seq data analysis results is often unclear. This is in part attributed to the two counter acting goals of (i) a cost efficient and (ii) an optimal experimental design leading to a compromise, e.g. in the sequencing depth of experiments. We introduce an R package called samExploreR that allows the subsampling (m out of n bootstraping) of short-reads based on SAM files facilitating the investigation of sequencing depth related questions for the experimental design. Overall, this provides a systematic way for exploring the reproducibility and robustness of general RNA-seq studies. We exemplify the usage of samExploreR by studying the influence of the sequencing depth and the annotation on the identification of differentially expressed genes. samExploreR is available as an R package from Bioconductor. v@bio-complexity.comSupplementary information: Supplementary data are available at Bioinformatics online.
ISSN:1367-4803
1367-4811
DOI:10.1093/bioinformatics/btw475