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Unweighted UniFrac distances were not different between the three sequence comparisons (Figure 3B). Figure 4 shows both UniFrac distances between the most used PCR condition in this study (annealing temperature 55°C and 25 cycles) and three PCR conditions.
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The tripodal template 2 is even more structured than 1 thus suggesting a significant interaction between the three sequences connected to the platform.
This sequence is highly conserved with nt sequence identities > 95% between the three sequences.
There was no significant difference between the three sequences (P > 0.373).
Incompatible sites were located within as well as between the three sequenced loci.
Polymorphism between the two sequence types was detected in 4 positions (4 SNP).
Again there is perfect conformity between the two sequence sets.
In sheep 333, there were differences in sequence distribution between the two sequence sub-sets.
Within genomic DNA, variation was also found between the two sequence datasets examined.
For all three eukaryotic comparisons, there was a highly significant positive correlation between the two sequence divergence levels (Table 3).
Comparisons between the two sequence groups at different time periods were performed using Student's t test.
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