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For example, if cyclical parthenogenesis has a higher rate of unequal crossing over or slip-strand mispairing than does meiosis, the consequence could be a higher frequency of tandem duplications during parthenogenesis; thus, a large proportion of duplicate genes would be expected to have arisen since the origin of parthenogenesis in this species.
Recent advances have suggested a new model termed subneofunctionalization, because neither neofunctionalization nor subfunctionalization can alone be explained in a large proportion of duplicate genes, and rapid subfunctionalization is often accompanied by prolonged and substantial neofunctionalization.
The proportion of duplicate image pairs that were missed ranged from 6.25% to 58.33%.
The proportion of duplicate image pairs that were split by misidentification varied widely between analysts.
In addition, the existing integration approach has resulted in a significant proportion of duplicate concepts being added to UMLS.
Furthermore, this over-calling of significant interactions becomes more problematic as the proportion of duplicate di-tags increases.
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After large-scale duplications, it has been shown that certain biochemical functions of some genes lead to preferential retention over others and that a larger proportion of duplicates are retained than after small-scale duplication (Blomme et al. 2006).
Plant genomes contain a high proportion of duplicated genes as a result of numerous whole, segmental and local duplications.
Similarly, they concluded that the proportion of duplicated reads is higher in multiple captured cells than in single-cells.
Limiting the comparison to muscle expressed genes in D. rerio, C. hamatus displayed a significantly higher proportion of duplicated genes.
The proportion of duplicated bases varied from 1.2%to6.9%9% across different chromosomes as showed in Additional file 2: Figure S3.
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