Validation of a commercially available test that enables the quantification of the numbers of CGG trinucleotide repeat expansion in FMR1 gene

被引:10
作者
Lim, Grace X. Y. [1 ]
Yeo, Minli [1 ]
Koh, Yvonne Y. [1 ]
Winarni, Tri Indah [2 ]
Rajan-Babu, Indhu-Shree [3 ]
Chong, Samuel S. [3 ,4 ,5 ]
Faradz, Sultana M. H. [2 ]
Guan, Ming [1 ]
机构
[1] BioFactory Pte Ltd, Singapore, Singapore
[2] Diponegoro Univ, Div Human Genet, Ctr Biomed Res, Fac Med, Semarang, Indonesia
[3] Natl Univ Singapore, Yong Loo Lin Sch Med, Dept Paediat, Singapore, Singapore
[4] Natl Univ Hlth Syst, Khoo Teck Puat Natl Univ Childrens Med Inst, Singapore, Singapore
[5] Natl Univ Singapore Hosp, Dept Lab Med, Singapore, Singapore
来源
PLOS ONE | 2017年 / 12卷 / 03期
关键词
FRAGILE-X-SYNDROME; EXPANDED ALLELES; PRIMED PCR; FULL MUTATIONS; GUIDELINES; IDENTIFICATION; DISORDERS; DIAGNOSIS; NEWBORN; ASSAY;
D O I
10.1371/journal.pone.0173279
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
In the present study, we evaluated a commercially available TP-PCR-based assay, the FastFraX(TM) FMR1 Sizing kit, as a test in quantifying the number of CGG repeats in the FMR1 gene. Based on testing with well characterized DNA samples from Coriell, the kit yielded size results within 3 repeats of those obtained by common consensus (n = 14), with the exception of one allele. Furthermore, based on data obtained using all Coriell samples with or without common consensus (n = 29), the Sizing kit was 97.5% in agreement with existing approaches. Additionally, the kit generated consistent size information in repeatability and reproducibility studies (CV 0.39% to 3.42%). Clinical performance was established with 198 archived clinical samples, yielding results of 100% sensitivity (95% CI, 91.03% to 100%) and 100% specificity (95% CI, 97.64% to 100%) in categorizing patient samples into the respective normal, intermediate, premutation and full mutation genotypes.
引用
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页数:15
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