Assessing the effect of the CLPG mutation on the microRNA catalog of skeletal muscle using high-throughput sequencing

(Downloading may take up to 30 seconds. If the slide opens in your browser, select File -> Save As to save it.)

Click on image to view larger version.

Figure 4.Figure 4.Figure 4.
Figure 4.

(A) Statistical significance [log(1/p)] of the affinity of ovine miRNAs in the DLK1–GTL2 domain for the 5′-UTR, coding sequence (ORF), and 3′-UTR of the ovine DLK1. The affinity was measured using either G- (blue) or M-scores (orange) as defined in the text. Bars are dark colored for highly expressed and light colored for lowly expressed miRNAs. The last pair of bars (“quad”) at the right of the graph corresponds to the quadrille scores, the remaining bars to the species scores and are labeled accordingly. P-values were determined using the sequence-shuffling test described in the text. Species scores require a Bonferroni correction for 127 independent tests. (B) Position in the DLK1 mRNA of target sites (8-mers, 7-mers, and 6-mers as defined by Grimson et al. [2007]) for the same set of miRNA species. (C) Same as in A except that the scores are “multiorganism (MO) scores” combining information from sheep, human, and mouse.

This Article

  1. Genome Res. 20: 1651-1662

Preprint Server