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The second avenue of forming interactions between duplicate gene products involves a non-homodimerizing protein that undergoes duplication.
The correlations between duplicate scans ranged from 0.886 to 0.998 and were similar between software versions.
Correlation analysis between duplicate probes (n = 85) present in the arrays showed perfect correlation (r2 = 0.98) indicating the reproducibility.
It is important and interesting to know how many sites, on average, may have been responsible for the functional divergence between duplicate genes.
The method errors showed that differences between duplicate measurements ranged from 0.04 to 0.12 mm. .
The variation between duplicate values was less than 5%.
Concordancy between duplicate samples was 100% for both SNPs.
In our hands, the correlation between duplicate experiments was statistically significant (see below).
The accuracy of the genotyping was determined by genotype concordance between duplicate samples.
Reproducibility between duplicate runs was evaluated using a binary comparison map.
Correlation coefficients calculated in dCHIP showed significant agreement between duplicate samples for all three genotypes analyzed.
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