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The data analysis from the two methods generated complementary insights that together created a more complete picture of a complex phenomenon.
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Although several studies demonstrated the presence of moderate to poor correlations between microarray and proteomic analyses [13], [14], [15], [16], implementing both methods may generate complementary and more informative data that cannot be obtained by either method alone.
Existing sequence-independent cloning methods require generating complementary single-stranded overhangs between the insert and the vector, a time-consuming and expensive process.
The addition of these methods would generate complementary data sets, ultimately increasing the depth, breadth, and accuracy of the analysis.
The two experimental sets we report generated complementary results.
However, such methods usually require generating complementary single-stranded overhangs in both the insert and vector fragments, with or without RecA-mediation [8], [12], [14].
A previous method generates complete complementary sequences with lengths of NnN n,N∈Z+).
These samples were used to generate complementary DNA (cDNA).
On a technical level, in spite of the depth possible with 454 FLX platform, the Sanger and pyro-based sequencing methodologies were complementary as each method generated sequences unique to each platform.
Different high-throughput methods render complementary data.
This method generated 575 publications.
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