Searching journal content for articles similar to Warner et al. 29 (6): 1036.

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  1. ...target expression variation and covariation, but these observations have been limited to a few microRNAs. Here we systematically study microRNA alternative functions in mouse embryonic stem cells (mESCs) by genetically deleting Drosha, leading to global loss of microRNAs. We apply complementary single...
  2. ...more peaks in introns than worms. The distribution of peaks in C. elegans is slightly farther upstream of the TSS than in Drosophila, perhaps reflecting the fact that for many C. elegans gene models the annotated TSS is the site of trans-splicing, with the start of transcription occurring further...
  3. ...for whole-animal transcriptome data (Ramani et al. 2011), the predominant class of alternative splicing in any given tissue in C. elegans is alternative 3′ or 5′ splice site usage (Fig. 3A).View larger version: In this window In a new window Figure 3. Summary and classification of tissue...
  4. ..., Cummings Life Science Center, Chicago, IL 60637, USA Corresponding author: watersto@uw.eduAbstractRecently developed single-cell technologies allow researchers to characterize cell states at ever greater resolution and scale. Caenorhabditis elegans is a particularly tractable system for studying...
  5. ...are less well understood. Here, we directly measure spatiotemporally resolved mRNA decay rates transcriptome-wide throughout C. elegans embryogenesis by transcription inhibition followed by bulk and single-cell RNA sequencing. This allows us to calculate mRNA half-lives within specific cell types...
  6. ...alternative splice forms, often with differential usage over the life cycle. We annotated internal promoter usage in operons using SL1 and SL2 data. We also uncovered correlated transcriptional programs that span >80 kb. These data provide detailed annotation of the C. elegans transcriptome. [Supplemental...
  7. ...These authors contributed equally to this work. Corresponding author: zyzhao@hkbu.edu.hkAbstractMassively parallel sequencing of the polyadenylated RNAs has played a key role in delineating transcriptome complexity, including alternative use of an exon, promoter, 5′ or 3′ splice site or polyadenylation site...
  8. ...nanopore-based direct RNA sequencing to characterize the developmental polyadenylated transcriptome of C. elegans. Taking advantage of long reads spanning the full length of mRNA transcripts, we provide support for 23,865 splice isoforms across 14,611 genes, without the need for computational...
  9. ...organization and establish reproducible gene expression programs. However, the field has been limited by the fact that most genomic studies in C. elegans have been performed on whole animals, which simultaneously capture both germline and somatic tissues and therefore can obscure germline-specific mechanisms...
  10. ...). Finally, loss of ADARs causes transcriptome-wide alternative splicing changes (Solomon et al. 2013; St Laurent et al. 2013; Mazloomian and Meyer 2015; Hsiao et al. 2018).Editing levels increase during development and vary between tissues, a phenomenon that cannot be explained by differential expression...
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