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4D-Dynamic Representation of DNA/RNA Sequences - A New Bioinformatics Method
* 1 , 2
1  Department of Radiological Informatics and Statistics, Medical University of Gdańsk, 80-210 Gdańsk, Poland
2  Department of Nuclear Medicine, Medical University of Gdańsk, 80-210 Gdańsk, Poland

Abstract:

A new method, 4D-Dynamic Representation of DNA/RNA Sequences, aiming at similarity/dissimilarity analysis of biological sequences, has been formulated. It belongs to a group of non-standard bioinformatics approaches called alignment-free methods. In the new method, sequences are represented by sets of material points in a 4D space - 4D-dynamic graphs. The method is a generalization of our previous 2D and 3D approaches [1,2]. In particular, 2D and 3D methods have been applied for the characterization of the complete genome sequences of viruses [3,4,5]. We call the methods dynamic, because the graphs are characterized by some values analogous to the ones used in the classical dynamics. In this work 4D moments of inertia are proposed as numerical characteristics (descriptors) of the 4D-dynamic graphs representing the sequences. 2D and 3D projections of the 4D-dynamic graphs are proposed as graphical representations of the sequences. 4D-Dynamic Representation of DNA/RNA Sequences has been applied to an analysis of the complete genome sequences of the 2019 novel coronavirus, available in March 2020 in GenBank. The proposed descriptors of the 4D-dynamic graphs proved to be very good. 4D moments of inertia correctly classify the sequences. The descriptors representing complete genome sequences of Deltacorovirus and of Betacoronavirus are located in different parts of the classification maps. The detailed classification of Betacoronaviruses to Embevovirus and the 2019 novel coronavirus is also recognized by the method. The descriptors representing Embevovirus and the 2019 novel coronavirus are also located in different parts of the maps.

References

[1]. Bielińska-Wąż, D.; Clark, T.; Wąż, P.; Nowak, W.; Nandy, A. 2D-dynamic representation of DNA sequences. Chem. Phys. Lett. 2007, 442, 140–144.

[2]. Wąż, P.; Bielińska-Wąż, D. 3D-dynamic representation of DNA sequences. J. Mol. Model. 2014, 20, 2141.

[3]. Panas, D.; Wąż, P.; Bielińska-Wąż, D.; Nandy, A.; Basak, S.C. 2D–Dynamic Representation of DNA/RNA Sequences as a Characterization Tool of the Zika Virus Genome. MATCH Commun. Math. Comput. Chem. 2017, 77 321–332.

[4]. Panas, D.; Wąż, P.; Bielińska-Wąż, D.; Nandy, A.; Basak, S.C. An Application of the 2D-Dynamic Representation of DNA/RNA Sequences to the Prediction of Influenza A Virus Subtypes, MATCH Commun. Math. Comput. Chem. 80 (2018) 295-310.

[5]. Bielińska-Wąż, D.; Panas, D.; Wąż, P. Dynamic Representations of Biological Sequences, MATCH Commun. Math. Comput. Chem. 82 (2019) 205-218.

Keywords: bioinformatics; alignment-free methods; data analysis; moments of inertia
Comments on this paper
Guillermin Agüero-Chapin
DNA/RNA Graphical Representations and Numerical Characterization
Dear Authors

What are the advantages of proposed 4D-Dynamic Representation of DNA/RNA Sequences in relation to the previous 2D and 3D-dynamic representations? Are they more resolutive than the previous ones?

Thanks in advance
Dorota Bielinska-Waz
Dear Prof. Guillermin Agüero-Chapin,

Thank you for your comment.
In particular, the similarity value can be split to four instead of two or three components, as in our previous 2D and 3D methods.
Each component of the similarity value can be traeted separately (jn particular in the correlation studies) or the components can be combined to one value
as in our previous work (Journal of Theoretical Biology 266 (2010) 667–674).

Yours sincerely,
Dorota Bielinska-Waz



 
 
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