Sentence examples for considered for mutations from inspiring English sources

Residues that were identified as conserved in more than 65% of 32 IFN- γ receptor sequences from 19 species were not considered for mutations.

Plasma samples could be considered for mutation analysis if tumour tissue is unavailable.

This is the first report of a critical role for SALL2 in eye morphogenesis in both humans and mice, and the gene should therefore be considered for mutation screening in patients with coloboma.

The families of these individuals were families that would have been considered for mutation screening of BRCA1 and BRCA2 if they had been identified through the ordinary oncogenetic reception, a clinical unit for oncogenetic counselling jointly run by the departments of oncology and clinical genetics at Lund University Hospital.

Further studies will be considered for segregating mutations for which more than one family shows rare segregating mutations in the same gene.

Macrosomic babies with diazoxide-responsive hyperinsulinism and a strong family history of diabetes (see characteristic 3 in the section above entitled Children and young adults with diabetes and a strong family history of diabetes: testing for HNF1A mutations) should be considered for HNF4A mutation screening.

On the other hand, a new fast algorithm will be considered for driver mutations prediction.

Genes with either moderate to strong protein expression in colon cancer in the Human Protein Atlas resource or with median values in the top 50 scores by either gene expression study were considered for cMS mutation analysis.

However, with an efficiency of 82.2%, which may be comparable [24] or higher [23] than reported elsewhere but remains low for a diagnostic test, and with the technical disadvantages described in Table 5, despite the low cost, dideoxy-sequencing can hardly be considered for point mutation detection in the FFPE diagnostic setting.

Therefore, while the most suitable detection sensitivity remains to be determined, the detection limit within 1 10% should be practically considered for RAS mutation testing.

As SAMtools does not clearly specify how to define the input for tumor and normal data sets and the generated result file lacked information about the somatic score, SAMtools was not further considered for calling somatic mutations.