Sentence examples for mutation by examining from inspiring English sources

To this end, one would need to test which of the individually isolated F2 animals are homozygous for the mutation by examining their F3 progeny.

We investigated the progenitor population for the small body size mutation by examining the PCA of 94 dog-derived SNP genotypes in a range of potential ancestral grey wolf populations.

A recent study addressed the concerns about the impact of the solubility-enhancing mutations by examining NBD1 crystal structures that had fewer and different solubilizing mutations (16).

In this study, we investigated the true frequency of ST7 gene mutations by examining 48 primary colorectal cancers, 48 primary gastric cancers that frequently show LOH on 7q31 (Nishizuka et al, 1997), and 48 primary hepatocellular carcinomas that show high-level expression of the ST7/RAY1 gene (Vincent et al, 2000; Zenklusen et al, 2001).

Jacob et al. developed and tested a new technique of correlated mutation analysis by examining codon sequences as well as amino acid sequences.

We then examined the sequence context in which these mutations occurred by examining the bases immediately 5′ and 3′ to the mutated bases.

Traditionally, somatic mutations are detected by examining DNA sequence.

The number of possible synonymous and non-synonymous mutations was derived by examining the longest annotated coding transcript per gene (transcript length based upon Ensembl Biomart described above).

Either way the estimates of variance explained by all SNPs represent a lower bound for the total additive genetic variability explained owing to incomplete LD between directly typed SNPs and causative mutations (33), and by examining all common SNPs jointly, power to detect the influence of a small number of moderate to weak effects is less compared with the joint effect of true causal loci alone.

Genotypes of individuals with symptoms of FXS and individuals at risk for carrying the mutation can be determined by examining the size of the trinucleotide repeat segment and the methylation status of the FMR1 gene.

The non-linearity in the median AUC as a function of mutation rate in the pairwise mutation model is partially explained by examining the proportion of families where performance improves versus degrades in Figure 8.