Searching journal content for articles similar to Tourasse et al. 27 (12): 2120.

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  1. ...RNA-seq compendium of reproducibly expressed splice junctions in C. elegans, assembled from 1682 publicly available RNA-seq experiments (Tourasse et al. 2017). Each splice junction has an associated percent spliced in (PSI) value, which is a measure of the frequency of each splice junction relative...
  2. ...Adam D. Warner, Louis Gevirtzman, LaDeana W. Hillier, Brent Ewing and Robert H. Waterston Department of Genome Sciences, School of Medicine, University of Washington, Seattle, Washington 98195, USA Corresponding author: watersto@uw.eduAbstractWe have used RNA-seq in Caenorhabditis elegans...
  3. ...of DAF-2-mediated development and longevity. Cell 154: 676–690. doi:10.1016/j.cell.2013.07.006 ↵Tourasse NJ, Millet JRM, Dupuy D. 2017. Quantitative RNA-seq meta-analysis of alternative exon usage in C. elegans. Genome Res 27: 2120–2128. doi:10.1101/gr.224626.117 ↵Weigelt CM, Sehgal R, Tain LS, Cheng J...
  4. ...,639 out of 52,846) identified using the long reads were also identified by meta-analysis of RNA-seq data (Tourasse et al. 2017) or were currently annotated in WormBase (Supplemental Fig. S1; Supplemental Table S1). Approximately half of the long reads were defined as full-length ones with these criteria...
  5. ...error rates and the relative lack of bioinformatics tools and analysis pipelines designed for long, error-rich reads.In this study, we have generated an atlas of postembryonic transcript structure using dRNA-seq to sequence RNA extracted from the major stages of the C. elegans developmental life cycle...
  6. .... 2011).Alternative polyadenylation is widespread in C. elegans, with ∼42% of genes possessing at least two 3′-UTR isoforms (Fig. 3A). The PAS usage is still most commonly the hexamer “AAUAAA,” which is used to process ∼58% of all C. elegans 3′ UTRs (Fig. 3B). We found that the remaining 42% possess...
  7. ...experiments (Nesvizhskii 2014).View larger version: In this window In a new window Figure 2. Novel protein-coding loci. Browser images show CDSs (open green rectangles), UTRs (pink), supporting PCCRs (red), top rank (black), cDNA evidence (brown), and RNA-seq–supported introns (blue rectangles). Additional...
  8. ...regulate the dynamics of mRNA stability during MZT (Yartseva and Giraldez 2015). To identify which pathways regulate each mRNA, we analyzed transcript levels during the first 8 h postfertilization (hpf), at 30- to 60-min intervals in wild-type zebrafish embryos using mRNA-seq (Supplemental Table S1). We...
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