Sentence examples for mutations in common from inspiring English sources

But two patients with the same type of cancer might have only five mutations in common.

We then screened primary or metastatic neuroendocrine breast carcinomas (excluding papillary and mucinous) for mutations in common cancer genes using polymerase chain reaction-mass spectroscopy (643 hotspot mutations across 53 genes), or semiconductor-based next-generation sequencing analysis (37 genes).

Genetic sequencing, which entered the popular lexicon with the launch of the Human Genome Project, in 1990, allows for the opposite type of search: comparing the entire genomes of people who suffer from an unknown disorder, to see if they have genetic mutations in common.

There are far more mutations in common tumors.

Cancer geneticist Garth Anderson (profiled in part 1 of this series) explains that the problem is the sheer number of ever-changing mutations in common tumors.

In the 'NGS & SNP6 matched' cluster (Figure 1), SNP6 data showed higher IBS mean and lower IBS variance, indicating that mutations in common variants was relatively less compared to NGS, an observation in line with the understanding that SNPs in the Affymetrix SNP 6.0 chip were supposedly well validated common polymorphisms.

They had one mutation in common, a substitution of aspartate in position 112 to glutamate (Asp112 → Glu).

Genetic DNA testing for neonatal diabetes revealed no pathogenic mutation in common KCNJ11, ABCC8 and INS genes.

One feature of the evolved xyloglucan binders is that all contained one mutation in common (aspartate to glutamate in position 112) compared to XG-34.

Finally, we propose that the roles of normal specific and mutation in common AS variants should be examined in addition to cancer-specific transcripts; analyses of these absent AS transcripts may further aid in the understanding of the cancer physiology.

Further association analysis using wild O. marmoratus (N = 68) and O. profundicola (N = 34) stocks revealed that they only had a single 430-bp insertion Y chromosome-specific mutation in common.