Sentence examples for variants will help from inspiring English sources

Additional studies regarding the different disease-causing variants will help us to gain a better understanding of the phenotypic variability observed among ALMS patients.

A comparison of the structures of neoculin and NBS His11-mutated variants will help to define the precise roles and interactions between His11 and His14 in taste modification.

The identification of these variants will help the development of new population-specific genotyping arrays.

New arrays with a higher proportion of low frequency variants will help to replicate the results of genome sequencing studies.

This variant will help us figure out the appropriateness of our choice of vector quantization to determine the starting point of our clusters in the feature space.

The frequency of G6PD deficiency was similar to other studies performed in Brazil and the finding of a predominant G6PD A− variant will help the clinical management of patients with drug-induced haemolysis.

Genetic diversity is usually considered a good thing: the more a population has, the more likely individuals will have gene variants that will help them adapt better to new climates, diets, and life-threatening diseases, such as malaria or smallpox.

Collectively, our presented database will allow further insights into the nature of functional variants and will help examine the path from genotype to phenotype.

To achieve the goal of using genetics in disease prevention and treatment, it is important to identify these functional genetic variants, which will help disentangle the complexity evident in common diseases and allow the development of new targeted medication.

Given the role of nt13708A in the MS, investigating the function of this common variant which will help to elucidate the pathogenesis of the disease.

Functional validation studies, if available, or at least the mutation prediction scores should be mentioned for the novel sequence variants identified, which will help create a comprehensive database of new likely-pathogenic variants.