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Similar diversification was also observed in the duplicate pair (LOC_Os10g33810 and LOC_Os02g41510) in rice.
However, limited diversification was also observed in genes present in the intrachromosomal region mainly involved in other Plasmodium specific functions such as invasion.
Micro-evolutionary diversification was also observed in GI 16, in which an internal deletion encompassing CDSs BPSS2057 to BPSS2076 was noted in four unique strains and both relapse isolates (Table 1).
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This extreme pattern of diversification in MPCR, which we refer to here as super-diversification, coupled with strong conservation in other regions was also observed in several other groups of SSSGP-encoding genes (Additional file 1, Figure S1) or cDNAs from Hessian fly (Table 1, Additional file 2, Figure S2).
Low sequence homology was also observed between A. americanum and a fellow member of the Acari, T. urticae, indicating significant diversification within this subclass.
Diversification of 25S rDNA distribution patterns is also observed in Paphiopedilum, but the numbers of loci and degree of dispersion is much lower than for 5S rDNA.
Addition/deletion of segments in intron I is also observed in elapid and hydrophiid genes and was linked to the evolutionary diversification of these snake toxin genes [ 28, 29].
Diversification was also influenced by gender of the household head (Table 2).
Despite the overall conservation of plastomes, genomic diversification was also experienced in many respects.
Diversification is also being pushed for munis.
Global diversification is also important.
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