Searching journal content for articles similar to Rowley et al. 30 (3): 447.

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  1. ...at sites bound by the C. elegans ortholog of NIPBL and loop extrudes in an effectively two-sided manner. ChIP-seq analyses show that cohesin translocation along the fountain trajectory depends on a fully intact complex and is extended upon WAPL-1 depletion. Hi-C contact patterns at individual fountains...
  2. ...://github.com/moshe-olshansky/EigenVector), topologically associating domains (TADs) using arrowhead (Rao et al. 2014), and chromatin loops using SIP (Supplemental Fig. S1C; Rowley et al. 2020). Replicates showed high similarity as measured by principal component analysis (PCA) (Supplemental Fig. S1D). We identified a total of 33,914 loops merged across...
  3. ...methods to identify different aspects of chromatin architecture. 3D organization—Digestion and ligation of 3D proximal loci are often used to identify long-range chromatin interactions -wide. Typical implementations include Hi-C (restriction enzyme digestion) and Micro-C (micrococcal nuclease [MNase...
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  4. ..., the time elapsed from the perturbation does not appear to affect the types of ENCODE cCREs involved in DegCre associations.Comparison of DegCre associations to Hi-C loopsWe sought to compare DegCre associations to Hi-C-derived loop calls from Reed et al. (2022), generated using Sip (Rowley et al. 2020...
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