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  1. ...of interacting fragments of RNA, which are then detected as chimeric reads by high-throughput sequencing. We reasoned that chimeras that represent intra- and intermolecular interactions can be distinguished from each other by an analysis of sequence overlap between the arms of each chimera.When an RNA molecule...
  2. ...the largest human protein titin. In particular, the XIST RNA contains many repetitive elements across the entire transcript, making it challenging to analyze. The simulated reads cover the full length of these three genes, including both exons and introns (Supplemental Fig. S1B). We focused on two...
  3. ...a transposase domain derived from an Hsmar1 insertion conserved in primates, providing functional DNA-binding to target methylation (Cordaux et al. 2006). Such exaptation and domestication events can often be identified by the occurrence of chimeric transcripts, which are mRNAs with both gene- and TE...
  4. ...-seq experiments showed that three of four retrocopies are capable of transcription from the sense strand relative to the parental genes. Analogously, by taking advantage of public strand-specific RNA-seq data from mosquito, chicken, zebrafish, and mouse (Methods), we found that recently evolved retrocopies...
  5. ...short-read RNA-seq as a modularized software that contains chimeric read extraction, fusion transcripts identification, expression quantification, gene fusion annotation, and interactive visualization. To benchmark existing tools, we collected or generated comprehensive simulation data sets to reflect...
  6. ...RNA genes, genomic parasites were coopted as new genes, and that both protein and RNA genes were composed from scratch (i.e., from previously nonfunctional sequences). These mechanisms then also contributed to the formation of numerous novel chimeric gene structures. Detailed functional investigations...
  7. ...manifests, for example, as alternative splicing within protein-coding genes, as well as in the discovery of thousands of long noncoding RNAs. It is also possible that significant numbers of human transcripts have not yet been described by annotation projects, while existing transcript models are frequently...
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  8. ...et al. 2011), long-range splicing and chimeric transcripts (Djebali et al. 2012b; Frenkel-Morgenstern et al. 2012), promoter-associated small RNAs (Affymetrix/Cold Spring Harbor Laboratory ENCODE Transcriptome Project 2009), and the splicing–chromatin connection (Tilgner et al. 2009), among other...
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  9. ...://www.yeast. org/. The transcripts were quantified and mRNA abundances recorded using Salmon, and the same set of reads used in the de novo assembly evaluation is described in “Analysis of assemblies generated from real reads.” To simulate transcript chimeras, 1000 transcripts were selected at random without...
  10. ...and produce a minimal set of putative transcript variants that have nonequivalent splicing structure and are compatible with the EST evidence. The resulting transcripts produced from ESTs are the ESTGenes as shown in the Ensembl Web site ( www.ensembl.org ). The algorithm can be applied to ESTs, mRNAs...
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