Ultra deep sequencing detects a low rate of mosaic mutations in tuberous sclerosis complex View Full Text


Ontology type: schema:ScholarlyArticle      Open Access: True


Article Info

DATE

2010-05

AUTHORS

Wei Qin, Piotr Kozlowski, Bruce E. Taillon, Pascal Bouffard, Alison J. Holmes, Pasi Janne, Susana Camposano, Elizabeth Thiele, David Franz, David J. Kwiatkowski

ABSTRACT

Tuberous sclerosis complex (TSC) is an autosomal dominant neurocutaneous syndrome caused by mutations in TSC1 and TSC2. However, 10-15% TSC patients have no mutation identified with conventional molecular diagnostic studies. We used the ultra-deep pyrosequencing technique of 454 Sequencing to search for mosaicism in 38 TSC patients who had no TSC1 or TSC2 mutation identified by conventional methods. Two TSC2 mutations were identified, each at 5.3% read frequency in different patients, consistent with mosaicism. Both mosaic mutations were confirmed by several methods. Five of 38 samples were found to have heterozygous non-mosaic mutations, which had been missed in earlier analyses. Several other possible low-frequency mosaic mutations were identified by deep sequencing, but were discarded as artifacts by secondary studies. The low frequency of detection of mosaic mutations, two (6%) of 33, suggests that the majority of TSC patients who have no mutation identified are not due to mosaicism, but rather other causes, which remain to be determined. These findings indicate the ability of deep sequencing, coupled with secondary confirmatory analyses, to detect low-frequency mosaic mutations. More... »

PAGES

573-582

References to SciGraph publications

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/s00439-010-0801-z

DOI

http://dx.doi.org/10.1007/s00439-010-0801-z

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1009924860

PUBMED

https://www.ncbi.nlm.nih.gov/pubmed/20165957


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