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While I use the IV estimation as the preferred specification, I also estimate additional models as explained in the empirical strategy section in order to compare results, establish a benchmark and assess the extent of the reverse causality problem.
I also estimate again the same regressions using the data from Özden et al.
I also estimate the benchmark model with larger samples, where I relax some data requirements.
I also estimate models of the impact of immigration on weekly wages (annual wages divided by weeks worked).
I also estimate models that instrument for immigration using shares predicted from state-specific historical settlement patterns.
To measure how layoffs may affect elasticity calculations, I also estimate separation elasticities based on involuntary separations.
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I also estimated a model that comprised a squared term of the variable 'parental support index'.
I also estimated the rate of entry of exogenous Aβ, applied in the ACSF.
I also estimated a third ω for the branch connecting the Drosophila and Sophophora groups because pairwise comparisons indicated consistently high rates of evolution along this branch (i.e., three branch labels in PAML, with Model = 2 and Nsites = 0; see Fig. 1).
I also estimated a GLM-regression adjusted posterior from each of the posterior samples [ 39].
To avoid potential biases in inferring the fraction of beneficial amino-acid fixations due to low levels of divergence, I also estimated α using divergence to a more distantly related species.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com