Searching journal content for articles similar to Fickett and Hatzigeorgiou 7 (9): 861.

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  1. ...GeneMark-ETP significantly improves the accuracy of automatic annotation of large eukaryotic s Tomáš Brůna1,4,5, Alexandre Lomsadze2,4 and Mark Borodovsky1,2,3 1School of Biological Sciences, Georgia Institute of Technology, Atlanta, Georgia 30332, USA; 2Wallace H. Coulter Department of Biomedical...
  2. ...found that G. lamblia assemblage A does not use any known auxiliary element (Bilodeau et al. 2022), highlighting the potential diversity of cleavage site recognition within the eukaryotic tree.View larger version: In this window In a new window Figure 1. Characterization of poly(A) signals in diverse...
  3. ...representation of eukaryotic translation complexity and focuses on locations critical for translation regulation. We show how RDGs can be used for depicting translated regions and for analyzing genetic variation and quantitative -wide data on translation for characterization of regulatory modulators...
  4. ...to predict specificities for uncharacterized TFs or TFs mutated in disease. Here we introduce recognition code learning via automated mapping of protein–DNA structural interfaces (rCLAMPS), a probabilistic approach that uses DNA-binding specificities for TFs from the same structural family to simultaneously...
  5. ...). Although two decades have passed since the first eukaryotic was sequenced, assigning translated ORFs to genetic loci remains a daunting task (Basrai et al. 1997; Claverie et al. 1997; Ladoukakis et al. 2011). Indeed, current annotations rely partly on ORF prediction algorithms that are only reliable...
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  6. ...) with myriad cis-regulatory elements scattered throughout pre-mRNAs. These molecular recognition events are critical for defining the protein-coding sequences (exons) within pre-mRNAs and directing spliceosome assembly on noncoding regions (introns). One of the earliest events in this process is recognition...
  7. ...outperformed local k-mer encoding by 10.19% in C. elegans, suggesting animals’ reliance on nucleotide-level chemical features for methylation recognition (Feng et al. 2010).Microbial groups displayed significant prokaryotic-eukaryotic differentiation. Prokaryotes (E. coli, G. subterraneus, G. pickeringii...
  8. ...positions within most eukaryotes (Fig. 1), and there is a corresponding paucity in the diversity of preferred recognition sequences observed for the characterized HD population (Berger et al. 2008; Noyes et al. 2008a). This focused sequence preference is similar to many other families of DNA-binding domains...
  9. ...Regulated post-transcriptional RNA cleavage diversifies the eukaryotic transcriptome Tim R. Mercer 1 , 4 , Marcel E. Dinger 1 , 4 , Cameron P. Bracken 2 , 3 , Gabriel Kolle 1 , Jan M. Szubert 2 , Darren J. Korbie 1...
  10. ...MutSꞵ 221 complex, which repairs larger insertions and deletions. Alternatively, if MSH6 and MSH2 form 222 an MMR recognition heterodimer MutSɑ, one to two base pair mismatches and indels are 223 repaired. MSH6 is found in P3, indicating a differential regulation of these portions of the MMR 224...
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