Sentence examples for mutations from one from inspiring English sources

A predictive approach for detecting likely β-mannosidosis is also demonstrated where we have extrapolated observed mutations from one species to homologous positions in other organisms based on the proximity of the mutations to the enzyme active site and their co-location from different organisms.

In ∂a∂i, all derived mutations from one genome are put into one pool or group to get a density distribution, which could be used to infer demographic history.

Hence, we have extrapolated observed mutations from one species and mapped them to homologous positions in other organisms.

The input to this problem are the VAFs for individual somatic mutations from one or more samples.

This has led to the development of mutation screens based on arrayed primer extension technology, which enable the simultaneous detection of multiple mutations from one individual.

In the process of evolution, the protein sequences gradually alter with the action of DNA mutations from one generation to the next.

The perfect phylogeny (PP) model utilizes the infinite sites assumption by building a tree of individuals -haplotypes- where all individuals evolve, with no recurrent mutation, from one common ancestor.

Since sporadic cases are mainly characterized by the presence of a single lesion, it is possible that sporadic cases with multiple lesions have inherited their mutation from one of their asymptomatic parents because of incomplete penetrance or have a de novo mutation.

Migration or introgression of a selected mutation from one breed to another leaves an unusual selection signature as shown by PLAG1 in Limousin where F ST between Limousin and other breeds is high except at the position of the selected mutation.

The main difference is that instead of defining the probability of mutation from one character state to another, the branch propagator g (x j,   t j | x i,   t i ) describes the likelihood of the lineage to connect an ancestor with fitness x i at time t i to a child with fitness x j at a later time t j (child in sense of a subclade in the tree, rather than direct offspring).

To correct for clonal expansion, a subset of the mutant plaques from the tissue sample is sequenced to identify recurrent mutations arising from one progenitor cell that may be inflating the mutant frequency.