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                  <mods:namePart>Bernaola-Galván, Pedro Ángel</mods:namePart>
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                  <mods:namePart>Carpena-Sánchez, Pedro Juan</mods:namePart>
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                  <mods:namePart>Gómez-Martín, Cristina</mods:namePart>
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                  <mods:namePart>Oliver, José L.</mods:namePart>
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               <mods:identifier type="citation">Bernaola-Galván P, Carpena P, Gómez-Martín C, Oliver JL. Compositional Structure of the Genome: A Review. Biology. 2023; 12(6):849. https://doi.org/10.3390/biology12060849</mods:identifier>
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               <mods:abstract>As the genome carries the historical information of a species’ biotic and environmental&#xd;
interactions, analyzing changes in genome structure over time by using powerful statistical physics&#xd;
methods (such as entropic segmentation algorithms, fluctuation analysis in DNA walks, or measures&#xd;
of compositional complexity) provides valuable insights into genome evolution. Nucleotide frequencies&#xd;
tend to vary along the DNA chain, resulting in a hierarchically patchy chromosome structure&#xd;
with heterogeneities at different length scales that range from a few nucleotides to tens of millions of&#xd;
them. Fluctuation analysis reveals that these compositional structures can be classified into three main&#xd;
categories: (1) short-range heterogeneities (below a few kilobase pairs (Kbp)) primarily attributed&#xd;
to the alternation of coding and noncoding regions, interspersed or tandem repeats densities, etc.;&#xd;
(2) isochores, spanning tens to hundreds of tens of Kbp; and (3) superstructures, reaching sizes of&#xd;
tens of megabase pairs (Mbp) or even larger. The obtained isochore and superstructure coordinates in&#xd;
the first complete T2T human sequence are now shared in a public database. In this way, interested&#xd;
researchers can use T2T isochore data, as well as the annotations for different genome elements, to&#xd;
check a specific hypothesis about genome structure. Similarly to other levels of biological organization,&#xd;
a hierarchical compositional structure is prevalent in the genome. Once the compositional&#xd;
structure of a genome is identified, various measures can be derived to quantify the heterogeneity&#xd;
of such structure. The distribution of segment G+C content has recently been proposed as a new&#xd;
genome signature that proves to be useful for comparing complete genomes. Another meaningful&#xd;
measure is the sequence compositional complexity (SCC), which has been used for genome structure&#xd;
comparisons.&#xd;
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               <mods:accessCondition type="useAndReproduction">Atribución 4.0 Internacional</mods:accessCondition>
               <mods:subject>
                  <mods:topic>Genoma humano</mods:topic>
               </mods:subject>
               <mods:titleInfo>
                  <mods:title>Compositional Structure of the Genome: A Review.</mods:title>
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