Searching journal content for articles similar to Mavrich et al. 18 (7): 1073.

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  1. ...be automatically determined from the fragment size distribution by a DPMM.SEM probabilistic modelSEM is based on a hierarchical GMM that describes the likelihood of observing a set of MNase-seq fragments from a set of nucleosomes. Each nucleosome contributes a distribution of reads surrounding its genomic position...
  2. ...with high splicing efficiency. Our data reveal a complex link between GC content, nucleosome positioning, and intron evolution in Paramecium.In eukaryotes, genomic DNA is compacted by histones into chromatin. The basic unit of chromatin is the nucleosome, which comprises a histone octamer made of the four...
  3. ...bodies. We then use the model as an in silico model of the yeast machinery to predict the effect of every single mutation along the . In doing so, we assign to every nucleotide a score representing its importance regarding the nucleosome positioning process. This genomic track is accessible at Git...
  4. ...-strandedness, which is most pronounced at transcript end sites, is dependent on high AT content and symmetrically positioned nucleosomes. We propose that sharp transitions in sequence composition at functional genomic elements constitute a common regulatory code and that DNA structure and propagation of torsional...
  5. ...by chemical cleavage-seq have a mean absolute occupancy of 90 ± 6% (±SD). Depending on nucleosome position calling procedures, there are 57,000 to 60,000 nucleosomes per yeast cell. The few low absolute occupancy nucleosomes do not correlate with highly transcribed gene bodies, but correlate with increased...
  6. ..., Spain Corresponding author: cpg@usal.es ↵ 3 These authors contributed equally to this work. Abstract In the yeast genome, a large proportion of nucleosomes occupy well-defined and stable positions. While the contribution of chromatin remodelers and DNA binding...
  7. .... It is unclear how chromatin structure survives disruptions caused by genomic replication or whether chromatin features are instructive of the transcription state of the underlying gene. We developed a method to monitor budding yeast replication, transcription, and chromatin maturation dynamics on each daughter...
  8. ...captured by sequence-based nucleosome positioning programs are reflected in PT values, we started from the control sequences. We randomly selected 5000–6000 genomic sequences from human and yeast s as 320-bp control sequences and found [nucmax] predicted nucleosome scores (dyad) within each region...
  9. ...development of animals and Dictyostelium but are absent in plants and yeast. These CHDs can mediate nucleosome translocation in vitro, but their in vivo mechanism is unknown. Here, we use -wide analysis of nucleosome positioning and transcription profiling to investigate the in vivo relationship between...
  10. ...-disfavoring sequence poly(dA/dT) around TF binding sites (TFBSs) significantly affects transcription in yeast (Raveh-Sadka et al. 2012), showing the importance of chromatin structure as a determinant of gene expression.In plants, -wide nucleosome positions have been determined for Arabidopsis thaliana (Chodavarapu et...
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