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In albatrosses, Abbott et al. [ 7] proposed that the gene conversion could have multiple recombination points, whereby certain duplicated portions were regularly homogenized while intervening sections remained unaffected and therefore evolved independently.
Our data are consistent with the gene conversion model outlined by Kumazawa et al. [ 26]; however, similar to Thalassarche albatrosses, multiple recombination points are needed to explain the non-concerted evolution of the 5' section of the control region [ 5].
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Recombination can occur at multiple locations in the genome, and multiple recombination events can contribute to the formation of a single genome.
The PHYLPRO graphical analysis showed multiple recombination signals with significant correlation values.
Eight recombination points were chosen on conserved aminoacids (Fig. 4A).
(During the 3 4 hour incubation step during which recombination was allowed, multiple recombination events may happen to a λdv molecule.
Thus, bootscan analysis of the HAdV-D53 genome shows evidence of multiple recombination events.
It suggested that multiple recombination including coa loci have occurred in S. aureus chromosome.
The occurrence of multiple recombination events is consistent with recent observations for differences in the recombination breakpoints between different HRV-Ca and HRV-Cc variants [19].
In this way recombination rates between each pair of adjacent loci can be specified, and multiple recombination events are permitted at any given position [62].
While the recombination points are essentially the same, arrows point to deviations between the haploid and SNP methods.
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