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• W2024558751 abstract "A novel system for copy number variation (CNV) analysis was developed in the present study using a combination of magnetic separation and chemiluminescence (CL) detection technique. The amino-modified probes were firstly immobilized onto carboxylated magnetic nanoparticles (MNPs) and then hybridized with biotin-dUTP products, followed by amplification with ligation-dependent polymerase chain reaction (PCR). After streptavidin-modified alkaline phosphatase (STV-AP) bonding and magnetic separation, the CL signals were then detected. Results showed that the quantification of PCR products could be reflected by CL signal values. Under optimum conditions, the CL system was characterized for quantitative analysis and the CL intensity exhibited a linear correlation with logarithm of the target concentration. To validate the methodology, copy numbers of six genes from the human genome were detected. To compare the detection accuracy, multiplex ligation-dependent probe amplification (MLPA) and MNPs-CL detection were performed. Overall, there were two discrepancies by MLPA analysis, while only one by MNPs-CL detection. This research demonstrated that the novel MNPs-CL system is a useful analytical tool which shows simple, sensitive, and specific characters which are suitable for CNV analysis. Moreover, this system should be improved further and its application in the genome variation detection of various diseases is currently under further investigation." @default.
• W2024558751 created "2016-06-24" @default.
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• W2024558751 date "2015-01-01" @default.
• W2024558751 modified "2023-09-29" @default.
• W2024558751 title "Copy Number Variation Analysis by Ligation-Dependent PCR Based on Magnetic Nanoparticles and Chemiluminescence" @default.
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• W2024558751 doi "https://doi.org/10.7150/thno.10117" @default.
• W2024558751 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/4265749" @default.
• W2024558751 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/25553099" @default.
• W2024558751 hasPublicationYear "2015" @default.
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