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Two additional figures were generated to verify the algorithm's thresholds.
Finite element (FE) models including debonding behavior in cohesive elements are generated to verify experimental results.
POSIX threads API and Linux FIFO scheduling policy are utilized to facilitate the design and Dhrystone-based tasks are generated to verify the design.
Melting curves were generated to verify the amplification specificity.
A melting curve analysis was generated to verify the specificity of the PCR amplification.
Two cell lines were generated to verify the response of predicted Wnt targets.
Following each run, melting curves were generated to verify specific product formation.
To confirm that the apparent absence of an IR was not a genome assembly artifact, PCR amplicons were generated to verify the region around the single rRNA operon.
Standard curves were generated to verify that the RT PCR assays had comparable amplification efficiencies (see Materials and Methods and Supplementary Material, Fig. S2).
After termination of the reaction by a final extension step at 72°C for 5 min, a DNA-melting curve was generated to verify the correct product by its specific melting temperature.
For seven strains that showed any potential phenotypic differences after curing and two that did not, additional cured replicates were generated to verify the phenotypes and observe the effects of potential additional mutations resulting from the curing process.
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CEO of Professional Science Editing for Scientists @ prosciediting.com