Sentence examples for mutations are easily from inspiring English sources

"The mutations are easily pinpointed changes in base pairs in DNA.

Although PTEN mutations are easily detectable, they are enriched in hypermutated tumors and may or may not cause loss of protein expression 12– 24.

MtDNA mutations are easily detected in early stage prostate cancer tissues and can also be found in the serum and urine from the same individuals [ 7].

Such point mutations are easily detected by mutation-detection systems such as the CEL1 nuclease assay or high-resolution melting curve (HRM) analysis [ 3, 4].

The m.3243A >G mutation is easily detected in urine, may cause a variety of mitochondrial syndromes (MELAS, maternally inherited diabetes and deafness, PEO, isolated MM, and cardiomyopathy), and its mutation load may even provide prognostic information (29).

The SSRs, which usually have a higher mutation rate, are easily genotyped using PCR, used as markers for phylogenetic analysis and in marker-assisted breeding when located on nuclear chromosomes.

In general, small premutations are more easily detected when the normal fragment is small and/or electrophoretic migration is long, whereas large/diffuse full mutations are more easily detected when the normal fragment is large and/or electrophoretic migration is short.

However, carbohydrate mutations are not easily classified in such terms.

However, the effects of mutations are not easily transferable among different influenza (H1N1) types and may need to be tested separately (Technical Appendix ).

Whole-exome (protein-coding exons plus other highly conserved regions) and whole-genome sequencing are beginning to be used for identifying genetic causes of rare, unknown conditions, particularly those presenting in childhood or in strongly affected pedigrees for which novel mutations are more easily detected.

With currently available techniques, construction of molecules that mimic ROS1 activating mutations in C. elegans are easily attainable, and would be a potentially informative approach to increase our understanding of the biology of this oncogene.