Sentence examples for mutations from all from inspiring English sources

To determine genes and domains frequently mutated in the patient populations, we first obtained the count of somatic mutations from all patients falling within the protein coding region of each gene, defined in the protein cancer set, and within each protein domain.

All models are trained using the whole data set (comprising therefore mutations from all amino acid types) but each of them corresponds to a different choice of input features.

The cpDNA haplotypes of both analyzed accessions were almost identical and unique, they differed by many mutations from all other Balkan species.

Furthermore, aggregating mutations from all genes containing a specific protein domain enables the identification of mutations that are rare at the gene level, but that occur frequently within the specified domain.

Yet, the power of our approach is derived from aggregating mutations from all genes containing a particular domain, therefore currently restricting our method to identifying significant mutation frequency inside domain regions.

Peptide nucleic acid-locked nucleic acid PCR clamp can rapidly (within 2 hours) detect EGFR mutations from all specimens used to diagnose lung cancers, that is, sputum, pleural effusion and bronchial washing which contain many normal cells.

In Table 6, which shows the frequencies of mutations resulting from all 12 possible mispairs for WT, E710A, and Y766A, the aggregate mutation frequencies at each template base (fourth entry for each template base) are broadly consistent with the expectations from our biochemical analysis.

I'm here suggesting that detailed data for all mutations taken from all "79" entries are provided to the community in the form of a table or downloadable flat or excel-type file.

DNA extracted from normal tissues from the same patient was genotyped for KRAS and/or BRAF mutation status from all cases with KRAS and/or BRAF mutation to distinguish between somatic and germline mutation.

Available preclinical studies so far are insufficient to support excluding all mutation carriers from all trials.

We generate simulated mutation data from all complete rooted binary trees with 3, 5, 7 and 9 nodes (Supplementary Appendix D.7).