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Thus, we proceed to identify two lower dimensional subsystems that govern the fast and slow dynamics in order to give us insight into the behavior of the full higher dimensional system.
Having constructed the strain-drug response graph we proceed to identify minimal hitting sets.
Once this core set was selected, we proceed to identify the subset of conditions where these genes are co-expressed.
With the centroids of P ^ and Q ^ translated to the origin, we proceed to identify the rotation in our algorithm.
After quantifying this using simulated data, we proceed to identify regions with excess San or Bantu ancestry found in TB cases but not in controls, and hypothesize that these regions may contain genes that affect TB susceptibility.
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Since a difference was found in the number of BrdU-IR cells, we proceeded to identify if these new born cells were glia or neurons.
We proceeded to identify statistically significant footprints.
Therefore, we proceeded to identify compounds that would increase the anti-cancer activity of TPT in HGS ovarian cancer cells.
Since the experimental capability to distinguish between the crystallographic domains had been established, we proceeded to identify and map the surface area artificially poled by the electric field.
As many physicians from the original sample turned out to be retired, dead or working outside Maputo upon contact, we proceeded to identify a further sampling fraction.
We proceeded to identify the putative RB69 gene(s) responsible for the seemingly allele-specific plating pattern of our λZAP II recombinant candidates.
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CEO of Professional Science Editing for Scientists @ prosciediting.com