Searching journal content for articles similar to Yaragatti et al..

Displaying results 1-10 of 54
For checked items
  1. ...-by-one testing limitation of these classic reporter assays, MPRAs add a DNA barcode that is transcribed if the sequence has regulatory activity and can be measured via RNA-sequencing (RNA-seq), providing a way to examine the functional effects of thousands of sequences in parallel (Patwardhan et al. 2009; Inoue...
    OPEN ACCESS ARTICLEACCEPTED MANUSCRIPT
  2. ...-seq in their respective tissue types (Supplemental Fig. S3B; Supplemental Table S2). This observation was further supported by our analysis of nucleosome-free regions (NFRs) (Tarbell and Liu 2019), which covered >48% of MHBs in 14 out of 17 tissue types (Supplemental Fig. S3C).Segmented DNA methylation states...
  3. ...the transcription start site [TSS]) exhibited similar signal intensities before and after injury globally (Supplemental Fig. S3E,F). This signal stability at the promoter regions suggests that the promoters of RRGs remain largely accessible, and other regulatory mechanisms may influence gene activation...
  4. ...et al. 2018), DNA topology (Teves and Henikoff 2014), and chromatin states (Santos-Rosa et al. 2002). It is therefore critical to assay active promoter and distal regulatory elements in a quantitative and sensitive manner when investigating biological phenomena, gene regulation, or regulatory...
  5. ...–dependent repair of erroneously incorporated nucleotides during pol α-dependent initiation of DNA replication of Okazaki fragments (Reijns et al. 2015), or of nucleotide excision repair (Sabarinathan et al. 2016), at sites where proteins, including TFs, bind DNA. In agreement with this hypothesis...
  6. ...IP-exo → WhIP-exo → PB-exo), site-specific protein-DNA interactions were altered that are manifested in quantitative and qualitative changes in the exonuclease stop sites.Promiscuous sites-specific binding on nucleosome-free DNAAbf1, Mcm1, Rap1, Cbf1, and Pho4 were assayed by PB-exo and ChIP-exo and analyzed...
  7. ...identifies accessible chromatin regions, which potentially harbor regulatory elements that can be used to characterize -wide DNA/TF interactions (Buenrostro et al. 2013). In combination, single-cell RNA-seq (scRNA-seq) and scATAC-seq technologies offer the potential to resolve dynamic changes...
  8. ..., Stanford, California 94305, USA Corresponding author: wjg@stanford.edu Abstract Transcription factors canonically bind nucleosome-free DNA, making the positioning of nucleosomes within regulatory regions crucial to the regulation of gene expression. Using the assay of transposase...
  9. ...DNA-guided establishment of nucleosome patterns within coding regions of a eukaryotic Leslie Y. Beh,1 Manuel M. Müller,2 Tom W. Muir,2 Noam Kaplan,3 and Laura F. Landweber1 1Department of Ecology and Evolutionary Biology, Princeton University, Princeton, New Jersey 08544, USA; 2Department...
  10. ...that it is a DNA binding transcriptional activator that is expressed at high levels in many different types of cancers, ZFX binding sites have not yet been mapped in cancer cells. To understand the mechanism by which ZFX may regulate the cancer transcriptome, we performed ChIP-seq, NOMe-seq, and RNA-seq assays...
For checked items

Preprint Server