Sentence examples for the variants among from inspiring English sources

Traditionally, the first few PCs are used in data analysis, since they retain most of the variants among the data features (in the original data set), and eliminate (by the projection) those features that are highly correlated among themselves; whereas the last few PCs are often assumed to retain only the residual noise in the data [23, 57].

The distribution and frequency of the variants among the eight scaffolds is shown in Figure  1.

Then, following the reconnection event, gene flow distributes the variants among populations to the point that they occur at similar frequencies in each population and the genetic compositions of populations are fully homogenized.

Differences in LD architecture encompassing the variants among different populations may help to fine-map the causal variant if shared across ethnicities, as shown in Palmer et al. (8).

Besides reconstructing longer contig, Meta-IDBA provides a multiple alignment of similar contigs from different subspecies in the same species, which represents the variants among genomes of these subspecies.

We have found that the variants among strains of VTEC O157 H7 isolated from cattle on farms linked to human cases of infection appear to constitute a closely related cluster of isolates, in contrast to isolates collected at slaughter and in the on-farm dairy cattle prevalence study.

In the present study we analyse the importance of the variant among breast cancer patients with a known familial disposition compared to sporadic cases and controls.

For example, if the pool size k increases from 3 to 30, the probability that only one chromosome carries the variant among 2 k chromosomes increases about eightfold from 0.03 and 0.22.

The goal of genetic studies is to understand the "architecture" of genetic influence and identify the causal variants among the many naturally occurring but phenotypically neutral variants.

The challenge of NGS in clinical practice is to identify the pathogenic variants among the many thousands of (new) variants that could be detected in each genome [Majewski et al., 2011].

An important consideration about NGS for diagnosis is identifying the pathogenic variants among the large number of variants detected.