Capturing Whole-Genome Characteristics in Short Sequences Using a Naïve Bayesian Classifier

  1. Rickard Sandberg1,2,3,
  2. Gösta Winberg1,2,
  3. Carl-Ivar Bränden1,
  4. Alexander Kaske2,
  5. Ingemar Ernberg1, and
  6. Joakim Cöster2
  1. 1Microbiology and Tumor Biology Center, Karolinska Institute, S-171 77 Stockholm, Sweden; 2Virtual Genetics Laboratory AB, S-171 77 Stockholm, Sweden

Abstract

Bacterial genomes have diverged during evolution, resulting in clearcut differences in their nucleotide composition, such as their GC content. The analysis of complete sequences of bacterial genomes also reveals the presence of nonrandom sequence variation, manifest in the frequency profile of specific short oligonucleotides. These frequency profiles constitute highly specific genomic signatures. Based on these differences in oligonucleotide frequency between bacterial genomes, we investigated the possibility of predicting the genome of origin for a specific genomic sequence. To this end, we developed a naïve Bayesian classifier and systematically analyzed 28 eubacterial and archaeal genomes. We found that sequences as short as 400 bases could be correctly classified with an accuracy of 85%. We then applied the classifier to the identification of horizontal gene transfer events in whole-genome sequences and demonstrated the validity of our approach by correctly predicting the transfer of both the superoxide dismutase (sodC) and the bioC gene from Haemophilus influenzaeto Neisseria meningitis, correctly identifying both the donor and recipient species. We believe that this classification methodology could be a valuable tool in biodiversity studies.

Footnotes

  • 3 Corresponding author.

  • E-MAIL rickard.sandberg{at}vglab.com; FAX 46-8-30-55-80.

  • Article and publication are at http://www.genome.org/cgi/doi/10.1101/gr.186401.

    • Received February 22, 2001.
    • Accepted May 25, 2001.
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