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Mitochondria are maternally inherited organelles, suitable for characterization of maternal relationships [11], [12], the traditional approach in familial genetics, identifying haplotypes and population groups [10], [13], [14], [15].
The second is that in many cases the approach taken is that of population genetics: identifying variation of interest within or between species, and then using whole organism genetics to identify the proportion of the variation that is genetic, and then using quantitative trait or association genetics to identify the genetic structure of the trait, and the dynamics of trait evolution.
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Population genetics identifies genetic variation and its distribution within and among populations, it reveals the demographic history of the populations studied, and can provide indirect insights into historical selection dynamics.
Dear Editor, In a recent article in Journal of Headache and Pain, Markus Schürks has reviewed current findings on migraine genetics identified by both candidate gene approaches and genome-wide association studies [1].
Molecular genetics identified a heterozygous NaV1.4 R1135H mutation.
Molecular genetics identified a homozygous NaV1.4 R1135C mutation that was heterozygous in her non-affected daughter.
Histopathologic lesions and molecular genetics identified a new strain of louping ill virus, 94% identical to the strain from Britain.
First, a report in Nature Genetics identified the PTHrP locus as a new breast cancer susceptibility gene.
Molecular genetics identified a heterozygous NaV1.4 R1135H mutation that seemed to be de novo as it was excluded in his non-affected parents.
Molecular genetics identified R1242G of the Cav1.1 voltage sensor in domain IV; such mutations in Cav1.1 have so far only been related to hypokalaemic periodic paralysis.
In fact, patterns-of-inheritance misconceptions represent the second most problematic conceptual category in genetics identified by Shaw et al. (2008).
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