Searching journal content for articles similar to Williams and Bowles 14 (6): 1060.

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  1. ...), presumably because deleting boundaries might destroy the insulating effect separating neighboring TADs. Thus, TAD boundaries share hallmarks of other functional genomic regions, like strong evolutionary constraints (Fudenberg and Pollard 2019). However, other than the dearth of deletions at TAD boundaries...
  2. ...examined gene neighbors without setting a threshold for genomic distance. However, when restricting to only those gene neighbors within 1 kb, we found a greater divergence between orthologs of coexpressed neighbors relative to the divergence observed in more distant genes (Supplemental Fig. S8). Second, we...
  3. ...network for the Arabidopsis thaliana transcriptome based on a modified graphical Gaussian model (GGM). Through partial correlation (pcor), GGM infers coregulation patterns between gene pairs conditional on the behavior of other genes. Regularized GGM calculated pcor between gene pairs among ∼2000 input...
  4. ...of significant BLAST hits against NCBI nr protein databank. Mapping of other ESTs and cDNAs on these genomic regions did not bridge the gap with already annotated neighboring genes. Mapping of short RNAs (sRNAs) on the total set of 76 npcRNA was performed using a large data set of massively sequenced A. thaliana...
  5. ...–protein interactions, protein complex, and comparative genomics data sets, in combinationwith similar lines of evidence fromorthologs inyeast, fly, andworm,were analyzed using an approach previously developed and validated for yeast (Lee et al. 2004, 2007a),C. elegans (Lee et al. 2008, 2010b), and Arabidopsis (Lee et...
  6. ...gene models was detected. A significant fraction of these expressed gene models are organized into chromosomal regions, about 100 kb in length, that exhibit a coexpression pattern. Compared with similar genome-wide surveys of the Arabidopsis transcriptome, our results indicate that similar...
  7. ...distribution using singletons with trans-PPIs (Table 4). The estimated P-values were adjusted by Bonferroni correction. Acknowledgments This work is supported by Science Foundation Ireland. References The Arabidopsis Genome Initiative. 2000. Analysis of the sequence of the flowering plant Arabidopsis thaliana...
  8. ...Research www..org Dhadi SR, Krom N, Ramakrishna W. 2009. Genome-wide comparative analysis of putative bidirectional promoters from rice, Arabidopsis and Populus. Gene 429: 65–73. Drosophila 12 Genomes Consortium. 2007. Evolution of genes and s on the Drosophila phylogeny. Nature 450: 203–218. Handoko L, Xu...
  9. ...editing by recruiting endogenous ADARs with antisense oligonucleotides. Nat Biotechnol 37: 133–138. doi:10 .1038/s41587-019-0013-6 Meyers BC, Vu TH, Tej SS, Ghazal H, Matvienko M, Agrawal V, Ning J, Haudenschild CD. 2004. Analysis of the transcriptional complexity of Arabidopsis thaliana by massively...
  10. ...the typical fate of any gene duplicate is loss ( Haldane 1933 ; Lynch and Force 2000 ). Arabidopsis thaliana, a dicot flowering plant (125-Mb with ∼26,000 annotated genes) ( The Arabidopsis Genome Initiative 2000 ), has retained duplicates in overlapping syntenous blocks that have been explained by multiple...
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