Papers › An investigation into inter- and intragenomic variations of graphic genomic signatures

An investigation into inter- and intragenomic variations of graphic genomic signatures

10 Mar 2015arXiv:1503.00162archive 2025-07-28

We provide, on an extensive dataset and using several different distances, confirmation of the hypothesis that CGR patterns are preserved along a genomic DNA sequence, and are different for DNA sequences originating from genomes of different species. This finding lends support to the theory that CGRs of genomic sequences can act as graphic genomic signatures. In particular, we compare the CGR patterns of over five hundred different 150,000 bp genomic sequences originating from the genomes of six organisms, each belonging to one of the kingdoms of life: H. sapiens, S. cerevisiae, A. thaliana, P. falciparum, E. coli, and P. furiosus. We also provide preliminary evidence of this method's applicability to closely related species by comparing H. sapiens (chromosome 21) sequences and over one hundred and fifty genomic sequences, also 150,000 bp long, from P. troglodytes (Animalia; chromosome Y), for a total length of more than 101 million basepairs analyzed. We compute pairwise distances between CGRs of these genomic sequences using six different distances, and construct Molecular Distance Maps that visualize all sequences as points in a two-dimensional or three-dimensional space, to simultaneously display their interrelationships. Our analysis confirms that CGR patterns of DNA sequences from the same genome are in general quantitatively similar, while being different for DNA sequences from genomes of different species. Our analysis of the performance of the assessed distances uses three different quality measures and suggests that several distances outperform the Euclidean distance, which has so far been almost exclusively used for such studies. In particular we show that, for this dataset, DSSIM (Structural Dissimilarity Index) and the descriptor distance (introduced here) are best able to classify genomic sequences.

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