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High-Throughput Multiplexed T-Cell–Receptor Excision Circle Quantitative PCR Assay with Internal Controls for Detection of Severe Combined Immunodeficiency in Population-Based Newborn Screening
Author(s) -
Jacalyn L. Gerstel-Thompson,
Jonathan F. Wilkey,
Jennifer C Baptiste,
Jennifer S Navas,
SungYun Pai,
Kenneth A. Pass,
Roger B. Eaton,
Anne Marie Comeau
Publication year - 2010
Publication title -
clinical chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.705
H-Index - 218
eISSN - 1530-8561
pISSN - 0009-9147
DOI - 10.1373/clinchem.2010.144915
Subject(s) - multiplex , dried blood spot , multiplexing , newborn screening , population , quality assurance , real time polymerase chain reaction , computational biology , medicine , biology , computer science , gene , bioinformatics , external quality assessment , pathology , genetics , telecommunications , environmental health
Real-time quantitative PCR (qPCR) targeting a specific marker of functional T cells, the T-cell-receptor excision circle (TREC), detects the absence of functional T cells and has a demonstrated clinical validity for detecting severe combined immunodeficiency (SCID) in infants. There is need for a qPCR TREC assay with an internal control to monitor DNA quality and the relative cellular content of the particular dried blood spot punch sampled in each reaction. The utility of the qPCR TREC assay would also be far improved if more tests could be performed on the same newborn screening sample.

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