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Simulated deletions are introduced into the data sets where the number of successive spacers being deleted is randomly chosen from the observed distribution of deletion length in the respective data set (supplementary table S1, Supplementary Material online).
A combination of T-DNA bintegrationtion and a certain deletion length in the recipient genome can contribute to the facilitation of high-throughput insertional mutagenesis by AMT.
Both analyses also yielded the significant interaction between deletion length and ethnicity.
Figure 1 presents a scatter plot of the relationship between total rare deletion length and FSIQ.
We computed the residual variance in FSIQ with variation associated with deletion length in each group was removed.
We found that rare deletion length predicted intelligence in our Anglo/White sample, but not in our Other Ethnicity sample.
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The lengths of gaps in the line plots indicate the deletion lengths with respect to the reference.
Structural variants were classified as "partial" whenever the sum of deletion lengths exceeded 3% of the consensus sequence.
We emphasize, then, that, while rare CNV deletion lengths covary differently for the two ethnic categories (possibly due to differences in parental SES), main effects of CNVs do not contribute to differences in cognitive performance of the two groups.
Our data show uniform random distribution of deletion lengths at the ND1/ND2 site across all ages.
In contrast, SRM predictions can in principle span the whole range of deletion lengths.
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