Searching journal content for articles similar to Batut et al. 23 (1): 169.

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  1. ....05.003 ↵Batut P, Dobin A, Plessy C, Carninci P, Gingeras TR. 2013. High-fidelity promoter profiling reveals widespread alternative promoter usage and transposon-driven developmental gene expression. Genome Res 23: 169–180. doi:10.1101/gr.139618.112 ↵Bell AC, West AG, Felsenfeld G. 1999. The protein CTCF...
  2. ...and validating the quantitative aspects of our data, we proceeded to evaluate the use of alternative promoters across tissues and the composition of each network module. Expression profiles from alternative TSCs of the same gene across the data set were generally independent, as evidenced by the low correlation...
  3. ...with TSSs that were exclusively proximal to CAGE peaks (CAGE-only genes) (Supplemental Table S2A) or were exclusively proximal to RAMPAGE rPeaks (RAMPAGE-only genes) (Supplemental Table S2B). Gene Ontology analysis revealed that the 6932 CAGE-only genes were enriched in terms such as T-cell receptor complex...
  4. ....5% of protein-coding genes contain two nonconstitutive exons that are separated by one or more constitutive exons. The question of coordination of multiple distant alternative sites is therefore relevant for many genes. We recently revealed a limited number of exon pairs that are distant in mRNAs but show...
  5. ...start sites (TSSs) and coregulated clusters of TSSs, commonly referred to as transcription start regions (TSRs). Usage of alternative TSSs is widespread (Davuluri et al. 2008; Reyes and Huber 2018) and results in mRNAs with shortened or lengthened 5′ untranslated regions (5′ UTRs), which can lead...
  6. ...% verified protein-coding genes. We corrected misannotation of translation start codon for 122 genes and suggested an alternative start codon for 57 genes. We found that 56% of yeast genes are controlled by multiple core promoters, and alternative core promoter usage by a gene is widespread in response...
  7. ...of transcripts (Pan et al. 2008; Barash et al. 2010; Brown et al. 2014; Söllner et al. 2017). The complexity and diversity of the transcriptome arises from the combinatorial usage of alternative promoters, exons and introns, and polyadenylation sites. A single gene can, therefore, encode a rich repertoire...
  8. ...al. 2011; The ENCODE Project Consortium 2012; Lu and Lin 2019). Transcription can be initiated from multiple TSSs in most genes, and alternative usage of TSSs in different cell types or growth conditions is prevalent in mammals, the fruit fly, and yeast (Davuluri et al. 2008; Batut et al. 2013; Lu...
  9. ...biosamples, and our results revealed that although the human-specific Alu elements are transcriptionally repressed, the older, expressed Alu elements may be exapted by the human host to function as cell-type–specific enhancers for their nearby protein-coding genes.Transposable elements and other repeats...
  10. ...by fragmentation, reverse transcription, and high-throughput sequencing. Millions of reads from sequencing are mapped back to a reference or transcriptome and quantified to estimate the expression of isoforms and genes (Mortazavi et al. 2008). Due to alternative splicing and the repetitiveness of genomic sequence...
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