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The explanatory disagreement involved different experimental approaches and divergent views on the nature of differentiation in early ontogeny (e.g., to what degree cells are pre-specified).
Points were also summed within 1 degree cells to investigate biases within FAO regions (higher resolution).
This method primarily labels cells in S-phase and to a minor degree, cells in the early portion of G2.
Data on population density and country-based key parameter data applied to populations in the 18,009 populated one degree cells were aggregated into these 240 ansectors.
A global anational database was constructed with one degree cells of latitude and longitude, and used to calculate densities for population and key health indicators.
Human habitation is found within the latitudinal range 84°N 58°S, by 360° of longitude, giving a grid with 51,480 one degree cells.
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In a second step, we calculated for both 0.5×0.5 degree cell size grids a SH expansion of the total intensity anomaly.
At the end of the merging process, we obtain a compilation of all available data on a global 0.05×0.05 degree cell size grid—(i.e. roughly 5×5 km cell size), with no missing values.
To build this model, we first reduced the size of the data set to a 0.2×0.2 degree cell size grid using the GMT function blockmedian applied on the compilation.
Then, the synthetic grid and the grid obtained as an output of the WDMAM merging process were sub-sampled on 0.5×0.5 degree cell size grids using the GMT function blockmedian.
The data presented here support a role for Stat92E in promoting cell division and to a lesser degree cell size in ept mutant eye disc cells.
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