Searching journal content for articles similar to Duttke et al. 29 (11): 1836.

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  1. ...for the convenience of modeling.Gene expression dataFor RNA-seq, total RNA-seq and poly(A) plus RNA-seq data in 19 human cell types were downloaded from ENCODE. Released transcript quantifications mapped to GRCh38 and annotated to GENCODE V29 were retained. RNA-seq gene expression was calculated as the sum of all...
  2. .... In brief, de novo identification of RNA editing sites requires more stringent criteria compared with the quantification of RNA editing status on known editing sites (Xu et al. 2023). The de novo identification method considers the sequencing coverage and number of alternative reads counts of both RNA...
  3. ...to standard methods; details are in Supplemental Methods. Relative quantification was performed using the method developed by Pfaffl (2001). Statistical testing was done with two-tailed t-tests using GraphPad Prism. All primer and sgRNAs are listed in Supplemental Table 4.Protein extraction...
  4. ...in the regulatory relationship between TP53 and TEs in cancer, focusing on the coopted promoter activity of TEs and transcript production.ResultsLeveraging LR-RNA-seq to identify TE loci with promoter potentialUsing long-read RNA sequencing (LR-RNA-seq) and short-read RNA sequencing (SR-RNA-seq), we confidently...
  5. ...-exonized transcript with a LINE/R1 element located in its seventh intron. The depth in exons, including the seventh intron, was assessed with RNA-seq from head tissue.In heads and larvae, ∼49% of the detected chimeric transcript isoforms were not assembled or had a contribution to gene expression <25% (Fig. 4B...
  6. ...exon, altering only the 3′ UTR sequence while leaving the protein-coding sequence unchanged. Because the 3′ UTR contains many essential regulatory elements—such as microRNA and RNA-binding protein (RBP) binding sites—variation in 3′ UTR length can modulate target mRNA function, stability...
  7. ...and lack flexibility in possible inputs. Nevertheless, this work has established the ability of correlational analysis to identify true CRE-to-gene associations at various distances.Application of correlational analyses to single-cell or single-nuclei multiomic data (RNA-seq and ATAC-seq on the same cell...
  8. ...), or other regulatory elements, and constitute a substantial portion of lincRNAs (Khorkova et al. 2015; Choudhary et al. 2023). Despite their potential importance, the transcriptomic landscape and clinical relevance of TE-derived elements in PAAD remain poorly characterized, partly due to limited sample...
  9. ...have highlighted the intricate interplay between ADAR enzymes and the MAVS pathway. For instance, it was shown that ADAR1 dampens MAVS signaling not only by editing the dsRNA but also through competitive binding of these substrates(Hu et al. 2023), underscoring the multifaceted regulatory role of ADARs...
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  10. ...regulatory 113 elements across vertebrates. 114 Results 115 In this study we examine the modulation of gene expression, chromatin accessibility and 116 histone modifications in Atlantic salmon following stimulation using poly I:C, a mimic of 117 infection with an RNA virus. A major transcriptomic response...
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