FEBS Letters
Volume 584, Issue 8 , Pages 1498-1502, 16 April 2010

Computational prediction of nucleosome positioning by calculating the relative fragment frequency index of nucleosomal sequences

Edited by Paul Bertone

  • Ryu Ogawa

      Affiliations

    • Institute for Advanced Biosciences, Keio University, Tsuruoka 997-0017, Japan
    • Systems Biology Program, Graduate School of Media and Governance, Keio University, Fujisawa 252-8520, Japan
  • ,
  • Noriyuki Kitagawa

      Affiliations

    • Institute for Advanced Biosciences, Keio University, Tsuruoka 997-0017, Japan
    • Systems Biology Program, Graduate School of Media and Governance, Keio University, Fujisawa 252-8520, Japan
  • ,
  • Hiroki Ashida

      Affiliations

    • Institute for Advanced Biosciences, Keio University, Tsuruoka 997-0017, Japan
    • Present address: Department of Computational Biology, Graduate School of Frontier Sciences, The University of Tokyo.
  • ,
  • Rintaro Saito

      Affiliations

    • Institute for Advanced Biosciences, Keio University, Tsuruoka 997-0017, Japan
    • Faculty of Environment and Information Studies, Keio University, Fujisawa 252-8520, Japan
    • Corresponding Author InformationCorresponding author: Address. Faculty of Environment and Information Studies, Keio University, Fujisawa 252-8520, Japan. Fax: +81 235 29 0525.
  • ,
  • Masaru Tomita

      Affiliations

    • Institute for Advanced Biosciences, Keio University, Tsuruoka 997-0017, Japan
    • Systems Biology Program, Graduate School of Media and Governance, Keio University, Fujisawa 252-8520, Japan
    • Faculty of Environment and Information Studies, Keio University, Fujisawa 252-8520, Japan

Received 3 December 2009; received in revised form 26 February 2010; accepted 26 February 2010. published online 03 March 2010.

Abstract 

We developed an accurate method to predict nucleosome positioning from genome sequences by refining the previously developed method of Peckham et al. (2007) [19]. Here, we used the relative fragment frequency index we developed and a support vector machine to screen for nucleosomal and linker DNA sequences. Our twofold cross-validation revealed that the accuracy of our method based on the area under the receiver operating characteristic curve was 81%, whereas that of Peckham’s method was 75% when both of two nucleosomal sequence data obtained from independent experiments were used for validation. We suggest that our method is more effective in predicting nucleosome positioning.

Abbreviations: SVM, support vector machine, ChIP, chromatin immunoprecipitation assay, ROC, receiver operating characteristic, AUC, the area under the ROC curve, HMM, hidden Marcov model, RFFI, relative fragment frequency index

Keywords: Nucleosome, Computational prediction, Support vector machine

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PII: S0014-5793(10)00171-7

doi:10.1016/j.febslet.2010.02.067

FEBS Letters
Volume 584, Issue 8 , Pages 1498-1502, 16 April 2010