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Subtracting the sequence bias from partially digested MNase-seq data reveals a general contribution of TFIIS to nucleosome positioning.

Gabriel GutiérrezGonzalo Millán-ZambranoDaniel A MedinaAntonio Jordán-PlaJosé E Pérez-OrtínXenia PeñateSebastián Chávez
Published in: Epigenetics & chromatin (2017)
The combination of partial MNase digestion and naked DNA correction of the sequence bias is a precise nucleosomal mapping method that does not exclude MNase-sensitive nucleosomes. This method is useful for detecting subtle alterations in nucleosome positioning produced by lack of TFIIS. Their analysis revealed that TFIIS generally contributed to nucleosome positioning in both gene promoters and bodies. The independent effect of lack of TFIIS on nucleosome occupancy and fuzziness supports the existence of alternative chromatin dynamics during transcription elongation.
Keyphrases
  • genome wide
  • single cell
  • transcription factor
  • high resolution
  • dna damage
  • copy number
  • electronic health record
  • dna methylation
  • rna seq
  • big data
  • mass spectrometry