In:
Molecular Genetics & Genomic Medicine, Wiley, Vol. 5, No. 4 ( 2017-07), p. 443-447
Kurzfassung:
Hereditary breast and ovarian cancer is characterized by mutations in BRCA 1 or BRCA 2 genes and PCR ‐based screening techniques, such as capillary sequencing and next‐generation sequencing ( NGS ), are considered gold standard methods for detection of pathogenic mutations in these genes. Single‐nucleotide polymorphisms ( SNP s) constitute a vast source of variation in the human genome and represent a risk for misdiagnosis in genetic testing, since the presence of a SNP in primer‐annealing sites may cause false negative results due to allele dropout. However, few reports are available and the frequency of this phenomenon in diagnostic assays remains unknown. Methods and Results In this article, we investigated the causes of a false negative capillary sequencing result in BRCA 1 involving a mother‐daughter dyad. Using several molecular strategies, including different DNA polymerases, primer redesign, allele‐specific PCR and NGS , we established that the initial misdiagnosis was caused by a SNP located in the primer‐annealing region, leading to allele dropout of the mutated allele. Conclusion Assuming that this problem can also occur in any PCR ‐based method that are widely used in diagnostic settings, the clinical report presented here draws attention for one of the limitations of genetic testing in general, for which medical and laboratory communities need to be aware.
Materialart:
Online-Ressource
ISSN:
2324-9269
,
2324-9269
DOI:
10.1002/mgg3.2017.5.issue-4
Sprache:
Englisch
Verlag:
Wiley
Publikationsdatum:
2017
ZDB Id:
2734884-2
