
Mosaic ratio quantification of isochromosome 12p in Pallister–Killian syndrome using droplet digital PCR
Author(s) -
Fujiki Katsunori,
Shirahige Katsuhiko,
Kaur Maninder,
Deardorff Matthew A.,
Conlin Laura K.,
Krantz Ian D.,
Izumi Kosuke
Publication year - 2016
Publication title -
molecular genetics and genomic medicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.765
H-Index - 29
ISSN - 2324-9269
DOI - 10.1002/mgg3.200
Subject(s) - isochromosome , biology , aneuploidy , fluorescence in situ hybridization , digital polymerase chain reaction , polymerase chain reaction , genetics , gene , chromosome , karyotype
Background Pallister–Killian syndrome ( PKS ) is a prototypic mosaic aneuploidy syndrome caused by mosaic supernumerary marker isochromosome 12p. Cells possessing the isochromosome 12p rapidly diminish after birth in the peripheral blood, often necessitating a skin biopsy for diagnosis. Therefore, a genomic testing that is capable of detecting low percent mosaic isochromosome 12p is preferred for the diagnosis of PKS . Methods The utility of the droplet digital PCR system in quantifying the mosaic ratio of isochromosome 12p in PKS was evaluated. Results Droplet digital PCR was able to precisely quantify isochromosome 12p mosaic ratio, and copy number measured by droplet digital PCR was correlated well with that of fluorescence in situ hybridization analysis. Conclusion Droplet digital PCR should be considered as an effective tool for both clinical and research analytics to precisely quantify mosaic genomic copy number alterations or mosaic mutations.