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GS is a form of MAS that selects favourable individuals based on genomic estimated breeding values.
GS is a form of MAS that selects favourable individuals based on genomic estimated breeding values (GEBVs).
In the breeding phase, genotype data are obtained in a breeding population, before favourable individuals are selected based on the genotype data obtained.
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The effect of imbalanced job polarization on individual-level mismatch was arguably favourable for individuals in non-crisis time, decreasing overeducation risk although also increasing the chances of undereducation, both gauged using the normative measure, but unfavourable during the global financial crisis of 2008 2009 and the following two years.
The main result is that the effect of imbalanced job polarization on individual-level mismatch was arguably favourable for individuals in non-crisis time (it decreases overeducation risk although it increases the chances of undereducation, both gauged using the normative measure) but unfavourable during the global financial crisis of 2008 2009 and the following two years.
Apomixis provides for the perpetuation of traits favourable to individual survival but eliminates the longer-term evolutionary advantage of biparental inheritance.
While this may be advantageous on a population level, there may be less favourable outcomes for individuals that harbour certain genotypes associated with excessive immune activation and inflammatory drive.
However, the balance of benefits and harms in such analysis (supplementary Online Tables W3 and W4, available at Annals of Oncology online) still appears favourable, although fewer individuals would benefit (and the same number would be harmed).
However, in the absence of a chronic antibiotic exposure sustaining resistance, these strains failed to disseminate despite the fact that environmental conditions and animal habits were highly favourable to inter-individual spread, and that contamination from humans to wildlife could recurrently occur at that site.
The log-rank test revealed that high CD4+ TILs, high CD8+ TILs, and high DC infiltration are each individual favourable prognostic predictors.
Miller generally advances the argument that the risk-benefit analysis therefore need not always be favourable to the individual patient, stating that 'clinical trials routinely administer interventions whose risks to patients are not compensated by medical benefits but are justified by the anticipated value of the scientific knowledge that might be gained'.
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