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Extensive gene decay has also taken place in many Boryong-repeated genes as in those of Ikeda.
Although extensive gene decay was reported for the S. citri genome (21% of the annotated coding sequences are truncated) (Carle et al. 2010), such phenomenon is not found in S. chrysopicola, S. syrphidicola, or S. melliferum.
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The genome analysis of the weakly pathogenic L99 serotype 4a provides extensive evidence of virulence gene decay, including loss of several important surface proteins.
The extensive genome variation due to gene decay observed in Shigella[ 13, 33] and Mycobacterium leprae[ 12] is a clear illustration of this point.
The rapid LD decay in Senegalese landraces compared to global accessions (Fig. 7) likely reflects extensive gene flow within Senegal.
"Extensive gene traffic on the mammalian X chromosome".
Particularly, extensive gene flow was observed between AG1, AG2, AI, and ANP.
Extensive gene rearrangements occur in the two species of Philopteridae.
Differences in L. casei genome inventory reveal both gene gain and gene decay.
Thus, a hierarchy in gene decay rates determines a pattern of relative gene expression levels.
Some duplicated genes underwent concerted evolution with extensive gene conversion.
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