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All measured parameters were found to be not significantly different and thus data from both populations were pooled (data not shown).
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The samples from both original populations were pooled, and then repeatedly randomly redistributed into two groups (500 times).
Both RNA populations were pooled in a 1 1 ratio to guarantee equal occurrence and putative constitutively expressed genes (glycerol phosphate dehydrogenase, gpdS; glucoamylase G2, accession number D49448) were used for normalization.
When DLC-sensitive populations were pooled and compared to pooled DLC-tolerant populations, multi-locus analyses did not distinguish the two groups.
When European populations were pooled, both Tajima's D (1.848) and Kelly's ZnS (0.207) were significant when recombination was included in the coalescence simulations.
When studies from both population based samples and high risk populations were pooled, white matter hyperintensities were associated with an increased risk of death during follow-up (2.0, 1.6 to 2.7, P<0.001; fig 4, also see web extra fig 5).
We found no differences (p>0.05 in all cases) and so the data from the two continental populations were pooled (hereafter Iberia).
Pairwise relatedness estimates from the primary and logged forest populations were pooled to increase sample sizes, but relatedness was calculated only between pairs of individuals from the same population.
Populations were pooled: Australia Papua New Guineaa (PNG); Southern Pacific (S'Pacific).
For example, a downward bias in Ne estimates was simulated by Palstra and Ruzzante (2011) when divergent populations were pooled.
In some previous studies e.g. [ 19] spores from multiple populations were pooled to infer a general mating strategy per species.
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