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We compared the magnitude of the increase in frequency between 1985 and 2004 for the MRC2 c.2904-2905delAG variant and the AHAP9 haplotype, with that of control variants/haplotypes matched for population frequency in 1985.
The approach outlined here could be utilized to expand the case cohort with additional samples of the same disease, even if not directly matched for population, in the same way as controls.
One village from each of 2 pairs matched for population size was randomly assigned to receive atole, which is a nutritious supplement that provided 6.4 g protein/100 mL and 91 kcal energy/100 mL.
DNA samples from 100 population control individuals matched for population ancestry (Spanish anonymous blood donors) were used to prepare reference pools (50 males and 50 females) for hybridization experiments.
For each replicate of data, we generate cases and controls from the same source population, together with additional samples from three external cohorts, not necessarily genetically matched for population.
Two Trial Areas were matched for population size, demographics including age and Aboriginality, and similar cancer incidence, based on the most recent available data (from 2006) when the trial was planned (figure 2 presents more recent data on population size from 2010).
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Summed populations were calculated as representative of a nation matched for the population during that period.
Each patient chromosome, transmitted by a given parent, is perfectly matched for the population of origin with the untransmitted chromosome of each heterozygous parent.
Some studies were carried out with populations matched for age [ 28], or comparing populations with pre-existing differences in executive function as detected by the Wisconsin Card sorting test [ 29], other studies were performed with differences for patients versus controls in number of years of study [ 31].
DNA samples obtained from a Caucasian population affected by breast cancer and a control population, matched for age and ethnicity, were genotyped for a polymorphism of the GSTZ1 gene.
A comparative experimental design, using a cross-sectional sample of ages from a healthy population, matched for sex and BMI was used.
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