Searching journal content for articles similar to Zhong et al. 26 (3): 351.

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  1. ...IP-seq, DNase-seq, and ATAC-seq (Krogan et al. 2006; Johnson et al. 2007; Shivaswamy et al. 2008; Lenstra et al. 2011; Weiner et al. 2012; Toenhake et al. 2018) to supplement GRNs (Zhong et al. 2016; Miraldi et al. 2019; Li et al. 2022). Despite these efforts, these methods do not have the capability...
  2. ...in LCL DNase-seq reads overlapping non-LCL DNase I hypersensitive (DHS) sites but not in LCL-specific DHS sites. Genome Research 1119 www..org DNase-seq predicts nucleosome positioning tribution of distances between pairs of reads in the combined data set exhibited the expected spacing on both...
  3. ...et al. 2019a), and methods like DNase-seq or ATAC-seq exaggerate accessibility differences, which was explained recently (Chereji et al. 2019b). Our absolute occupancy measurements clarify this method-driven misconception. Nonetheless, anecdotal reports of nucleosome depletion over highly transcribed...
  4. ..., and FAIRE-seq signal at PcG-occupied (n = 4020) or PcG-free (n = 10,251) CGI promoters, centered on TSSs. Input for ATAC-seq and DNase-seq represents digestion of naked genomic DNA by Tn5 or DNase I, respectively. (E) A metaplot analysis at CGI intervals (±20%) for CGI-positive TSSs with (PcG) or without...
  5. ...transcription. Although a -wide allele-specific chromatin accessibility map had recently been generated using DNase-seq and ATAC-seq in mammal (Lu et al. 2016; Wu et al. 2016), a global pattern of allele-specific nucleosome occupancy has not been reported in any other high eukaryotic species. Here, we reported...
  6. ...on the chromosomes during mitosis (Black et al. 2016; Teves et al. 2016; Liu et al. 2017b). Second, a -wide DNase-seq experiment revealed that accessibility is widely preserved and only locally modulated during mitosis (Hsiung et al. 2015). Finally, a recent study utilized 5-EU labeling to demonstrate that many...
  7. ...structured around nucleosomes. (A) ATAC-seq (green) insertion track for S. cerevisiae shows enrichment of insertions at accessible chromatin regions, similar to DNase-seq cut density (orange). Both tracks were smoothed by 150 bp and scaled so that the maximum density in the region is 1. (B) Fragment...
  8. ..., modeling 3D chromatin organization, and predicting gene expression (Thibodeau et al. 2021; Karbalayghareh et al. 2022; Tan et al. 2023; Zhang et al. 2023; Grover et al. 2024). Although experimental assays such as FAIRE-seq (Giresi et al. 2007), DNase-seq (Song and Crawford 2010), and ATAC-seq (Buenrostro...
  9. ...model. (G) Visualization of m6A calls in the HMBS locus that are unique to fibertools (purple), unique to the subread GMM model (red), or shared by both (gray). Reads are sorted by the number of CCS passes (low to high). DNase-seq (ENCODE July 2012 Freeze) and CAGE signals are shown above...
  10. ..., such as DNase-seq or FAIRE-seq. We observed that phasing occurs in all cell types, although it remains unclear what is dictating the precise organization that is evident at NDRs and even at absent NDRs (f NDRs). The first possibility is a sequence-based propensity for DNA to be associated with nucleosome...
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