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We hypothesized that, like protein-coding genes, miRNAs (including RrmiRs) may also duplicate and expand accompanying large genomic SD events in their evolutionary history.
Whole chromosomes and whole genomes may also duplicate by various mechanisms.
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Some of these genes may also be duplicated in several specific taxa and thus, have the potential of being phylogenetically discrepant [13], [14], [15], [16], [17], [18].
Single genes may also have duplicated independently multiple times, within established loci and to create new loci, prior to and following formation of new gene structures.
These results suggest a core MHC region is contained on chromosome 13q, but there may also be duplicated regions on chromosomes 4 and 6 as well as on 2 microchromosomes.
The other two Populus blocks in LG_I and LG_XII may also represent duplicated regions since one of the genes matched to the same peach sequence and the rest matched to the sequences that are anchored to the same position in the TxE map.
Unique genes may also be duplicates that diverged too much to be distinguished now [ 22].
Conversely, in a minority of cases (less than 1%), it may also be duplicated, particularly when the middle meningeal artery is also duplicated.
The same simulated data vector was also duplicated for localities where data had been duplicated.
SIX13 is also duplicated.
All steps were also duplicated.
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