Abstract
Motivation: 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. Results: 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.
| Originalsprache | Englisch |
|---|---|
| Seiten (von - bis) | 3345-3347 |
| Seitenumfang | 3 |
| Fachzeitschrift | Bioinformatics |
| Jahrgang | 32 |
| Ausgabenummer | 21 |
| DOIs | |
| Publikationsstatus | Veröffentlicht - 1 Nov. 2016 |
| Extern publiziert | Ja |
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