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10.3109/10409238.2015.1051505

http://scihub22266oqcxt.onion/10.3109/10409238.2015.1051505
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C4580520!4580520 !26038153
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suck abstract from ncbi


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pmid26038153
      Crit+Rev+Biochem+Mol+Biol 2015 ; 50 (4 ): 269-83
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  • Protein-DNA binding in high-resolution #MMPMID26038153
  • Mahony S ; Pugh BF
  • Crit Rev Biochem Mol Biol 2015[]; 50 (4 ): 269-83 PMID26038153 show ga
  • Recent advances in experimental and computational methodologies are enabling ultra-high resolution genome-wide profiles of protein-DNA binding events. For example, the ChIP-exo protocol precisely characterizes protein-DNA cross-linking patterns by combining chromatin immunoprecipitation (ChIP) with 5' ? 3' exonuclease digestion. Similarly, deeply sequenced chromatin accessibility assays (e.g. DNase-seq and ATAC-seq) enable the detection of protected footprints at protein-DNA binding sites. With these techniques and others, we have the potential to characterize the individual nucleotides that interact with transcription factors, nucleosomes, RNA polymerases and other regulatory proteins in a particular cellular context. In this review, we explain the experimental assays and computational analysis methods that enable high-resolution profiling of protein-DNA binding events. We discuss the challenges and opportunities associated with such approaches.
  • |*Models, Molecular [MESH]
  • |Animals [MESH]
  • |Chromatin Immunoprecipitation/trends [MESH]
  • |Chromatin/chemistry/*metabolism [MESH]
  • |Computational Biology/trends [MESH]
  • |Computer Simulation/trends [MESH]
  • |DNA Footprinting/trends [MESH]
  • |DNA-Binding Proteins/chemistry/*metabolism [MESH]
  • |DNA/chemistry/*metabolism [MESH]
  • |Datasets as Topic [MESH]
  • |Exodeoxyribonucleases/metabolism [MESH]
  • |Expert Systems [MESH]
  • |Genomics/methods/trends [MESH]
  • |Humans [MESH]
  • |Hydrolysis [MESH]
  • |Nucleic Acid Conformation [MESH]
  • |Nucleosomes/chemistry/metabolism [MESH]
  • |Protein Conformation [MESH]


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