Sentence examples for mutations it carries from inspiring English sources

Following the implementation in SFS_CODE (Hernandez 2008), the fitness of each individual is the product of the fitness effect of the mutations it carries, which for a mutation with selection coefficient s (s < 0 for deleterious mutations) is 1 + s in heterozygotes and (1 + s) in homozygotes.

When pJM11 was assayed, it had no −61 band, presumably due to the multiple mutations it carries, and showed no changes in band pattern beyond those caused by Mor binding, providing no evidence for or against His-α interaction with the DNA.

After mutation we get: p ˜ (i, X ) = ∑ j = 0 i p (j, X ) p (d = i − j ),  where  d ~ P o i s s o n (U ) The probability ω of survival of a young individual depends only on the number i of mutations it carries: ω i = e- is, where s is the strength of natural selection against each deleterious mutation.

Once a positive individual is found it is sequenced to determine the exact mutation it carries.

Thus, familial PrDs contrast with CAG-repeat diseases because a single gene can cause multiple diseases depending on which mutation it carries.

We hypothesize that the growth of M184 is impaired because of one or more of the other mutations that it carries.

The relationship between causal mutations and the haplotypes have been regarded as a tool for genetic researches----first finding association to a haplotype, and then subsequently identifying the causal mutations that it carries [ 49].

For example, strain 'Newman' is a clinical isolate that forms weak biofilms, most likely as it carries mutations in the coding regions for the Fnbp proteins (vide infra) (Grundmeier et al. 2004).

Furthermore, STY2 is an attenuated strain, CVD908- htrA [ 3], which differs from STY1 in that it carries additional mutations in aroC aroD, and htrA [ 25].

The p53 in Huh7 cells and cell lines derived from it carries a mutation at codon 220 (Y220C) which has been shown to be transcriptionally inactive [ 13– 15].

This sequence seems to represent the remnant of an IS Mmy2 without transposase activity because it carries a mutation disrupting the transposase gene.