Method and theory of genome profiling (GP) developed for identification and classification of organisms

17 October 2024, Version 1
This content is a preprint and has not undergone peer review at the time of posting.

Abstract

Details of the method and theory on the genome profiling (GP), which provides with the method for species identification and classification of organisms, are first described. GP consists of three major steps: i.e., random PCR, micro-temperature gradient gel electrophoresis (μTGGE), and extraction and processing of featuring points contained in genome profiles (results of the former step) generating species identification dots (spiddos). Methodological, physical and biological meanings of ‘random PCR’, ‘μTGGE’, ‘spiddos’, ‘genome distance (dG)’ and others introduced in this study are originally discussed. This paper gives a base for understanding the diversity of GP achievements performed for 30 years written in an alternative review on GP (i.e., to appear in Briefings in Functional Genomics (in process)), especially underscoring the importance of the spiddos parameter for calculating closeness of species and constructing genome database. Spiddos contains such a kind of information termed as SIOWS (sequence information obtained without sequencing), which is essentially unique and important for the GP technology, derived from the sequence-specific DNA melting phenomenon together with DNA melting theory. Succeedingly, one can understand why GP enables us to draw the sufficient amount of information without sequencing of genomic DNA. This also explains why identification/classification of species can be so readily and universally done by GP. It requires the perspective on the nature of spiddos. Since this paper first provides detailed procedures of GP and in-depth theoretical explanation of the GP-related phenomena, a wide range of scientists (Bacteriology, Infectious Disease Medicine, Epidemiology, Environmental Science, Biodiversity Science, Mutagen Research, Taxonomy, Bio-database Science, and others) can engage in applications of GP, which is difficult without sufficient understanding of the method and theory of GP.

Keywords

random PCR
DNA melting
species identification
species classification
bio-database

Comments

Comments are not moderated before they are posted, but they can be removed by the site moderators if they are found to be in contravention of our Commenting Policy [opens in a new tab] - please read this policy before you post. Comments should be used for scholarly discussion of the content in question. You can find more information about how to use the commenting feature here [opens in a new tab] .
This site is protected by reCAPTCHA and the Google Privacy Policy [opens in a new tab] and Terms of Service [opens in a new tab] apply.