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  1. .... Observation of dually decoded regions of the human using ribosome profiling data. Genome Res 22: 2219–2229. doi:10.1101/gr.133249.111 ↵Michel AM, Andreev DE, Baranov PV. 2014. Computational approach for calculating the probability of eukaryotic translation initiation from ribo-seq data that takes into account...
  2. ...), as described at http://creativecommons.org/licenses/bync/4.0/. Research 1836 Genome Research 25:1836–1847 Published by Cold Spring Harbor Laboratory Press; ISSN 1088-9051/15; www..org www..org experiments in human U2OS cells and compared these results with RNA-seq. Ribosome profiling is based on the protection...
  3. ...compared footprints in other genomic regions and observed major differences in small noncoding RNAs (Supplemental Fig. S3A); 11.5% of our RNase footprinting reads were mapped to small noncoding RNAs, which is 3.7-fold that of ribosome profiling (Supplemental Fig. S3A–C). These reads were found within...
  4. ...), whereas for AASDHPPT, ribosome profiling data suggest that initiation at sAUG is greater than at fdAUG, contrary to our reporter assay (Fig. 4D). For intact GWIPS-viz screenshots of each of the 10 genomic loci, see Supplemental Figures S3–S12. A certain level of disagreement between the two approaches...
  5. ...are used (a situation confounded by the occurrence of AS) (Tanner et al. 2007; Brosch et al. 2011; Ezkurdia et al. 2012). Ribosome profiling (RP) is a newer technique designed to infer translated regions of RNA molecules (Ingolia et al. 2009). Essentially, the short portion of an RNA that is bound...
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  6. ...” in the other frame a new stop codon that is now decoded by the ribosome (i.e., frameshift-driven events) (Supplemental Table S9).In direct splice-driven events, the stop codon availability is dictated by the actively transcribed regions that contain the stop codon. We find this scenario for 72% (8877 of 12...
  7. ....114. 24:1977–1990 Published by Cold Spring Harbor Laboratory Press; ISSN 1088-9051/14; www..org Genome Research 1977 www..org Figure 1. Transcriptome profiling and CLIP-seq confirm that transposable elements (TEs) are the main direct targets of PIWI-mediated regulation. (A) Bioinformatic prediction...
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