University of Illinois Chicago
Browse

Encoding DNA sequences by integer chaos game representation

Download (1.09 MB)
journal contribution
posted on 2019-04-18, 00:00 authored by Changchuan Yin
Motivation: DNA sequences are fundamental for encoding genetic information. The genetic information may be understood not only by symbolic sequences but also from the hidden signals inside the sequences. The symbolic sequences need to be transformed into numerical sequences so the hidden signals can be revealed by signal processing techniques. All current transformation methods encode DNA sequences into numerical values of the same length. These representations have limitations in the applications of genomic signal compression, encryption, and steganography. Results: We propose an integer chaos game representation (iCGR) of DNA sequences and a lossless encoding method DNA sequences by the iCGR. In the iCGR method, a DNA sequence is represented by the iterated function of the nucleotides and their positions in the sequence. Then the DNA sequence can be uniquely encoded and recovered using three integers from iCGR. One integer is the sequence length and the other two integers represent the accumulated distributions of nucleotides in the sequence. The integer encoding scheme can compress a DNA sequence by 2 bits per nucleotide. The integer representation of DNA sequences provides a prospective tool for sequence analysis and operations.

History

Publisher Statement

This is a copy of an article published in the Journal of Computational Biology ©2017, Copyright Mary Ann Liebert, Inc.; Encoding DNA sequences by integer chaos game representation is available online at: http://www.liebertonline.com.

Citation

Yin, C. (2019). Encoding and decoding DNA sequences by integer chaos game representation. Journal of Computational Biology : A Journal of Computational Molecular Cell Biology, 26(2), 143-151. doi:10.1089/cmb.2018.0173

Publisher

Mary Ann Liebert

Language

  • en_US

issn

1066-5277

Issue date

2017-12-19

Usage metrics

    Categories

    No categories selected

    Exports

    RefWorks
    BibTeX
    Ref. manager
    Endnote
    DataCite
    NLM
    DC