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Our method also detects many long-time delayed interactions.
As expected, our more sensitive method also detects activations of specific signaling circuits in pathways which were non-significant in FSC tests.
(Note that this method also detects purO mutants, but their contribution was ignored because they are ∼1000-fold ∼1000-fold purarerthans).
Second, while the standard ChIP protocol reliably yields higher enrichment values at DSTs in targeted experiments, the modified method also detects σ binding at 2 out of 4 DSTs tested.
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(4) Our method also detect outlier arcs which are smoothly connected to inlier arcs.
In addition, the method also detected PIV3 genomes in specimens found negative by culture confirmation, indicating the value of this RT-PCR assay.
The former method also detected negative selection on codon 32, while both methods detected such selection on codon 99 (the two positions are invariant in the complete data set).
The end-labeling method also detected strong signals at Ty elements.
Phylogenies constructed with this method also detected the same sequence classes reported in this study.
Our ATE method also detected many other similar pairs such as { NIT1, DEDD} pair on Chr.
Our method also detected an overlapping functional module with only one gene (KIAA0242) difference to model 1.
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