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Methods detecting rhythmic gene expression are biologically relevant only for strong signal

Fig 2

Fewer time points per cycle lead to a weaker detection of rhythmic patterns even if the transcriptome profiling quality is better.

a) Bhlhe41, Npas2, and Per1 expression over time from data of the same mouse experiment [2] using two transcriptome profiling techniques: microarray vs RNAseq. The number of time-points with data is 24 for microarray and 8 for RNAseq. b) The restriction of microarray time-series to the same time-points as in the RNAseq series produces similar p-value distributions to those obtained with RNAseq. This supports a major role of the temporal resolution for method results, relative to a minor role for the difference between RNAseq and microarrays. Mouse image credit to Anthony Caravaggi (license CC BY-NC-SA 3.0).

Fig 2

doi: https://doi.org/10.1371/journal.pcbi.1007666.g002