Sample Tracking Tool: A Comprehensive Approach Based on OpenArray Technology and R Scripting for Genomic Sample Monitoring.

IF 3.3 3区 医学 Q1 MEDICINE, GENERAL & INTERNAL Diagnostics Pub Date : 2025-01-10 DOI:10.3390/diagnostics15020149
Giulia Trastulli, Giulia Calvino, Bruno Papasergi, Domenica Megalizzi, Cristina Peconi, Stefania Zampatti, Claudia Strafella, Carlo Caltagirone, Emiliano Giardina, Raffaella Cascella
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Abstract

Background/Objectives: Centralizing genetic sequencing in specialized facilities is pivotal for reducing the costs associated with diagnostic testing. These centers must be able to verify data quality and ensure sample integrity. This study aims at developing a protocol for tracking NGS-analyzed samples to prevent errors and mix-ups, ensuring proper quality control, accuracy, and reliability in genetic testing procedures. To this purpose, a protocol based on the genotyping of a panel of 60 single-nucleotide polymorphisms (SNPs) by OpenArrayTM technology was employed. Methods: The protocol was initially tested on a cohort of 758 samples and subsequently validated on a cohort of 100 samples. Furthermore, its ability to accurately detect identical and different samples was evaluated through a simulation test conducted on an additional 100 samples. Results: In total, 55 probes achieved a call rate ≥90% and were subjected to the sample matching process performed by an R tool specifically developed. The SNP panel achieved a random match probability of 3.29 × 10-15, proving its suitability for efficiently tracking samples and rapidly identifying any errors or mix-up during the analytical processing. Conclusions: The features of OpenArrayTM technology, cost-effectiveness, rapid analysis, and high discriminative power make it a suitable tool for sample tracking. In conclusion, this method represents a valuable example for promoting laboratory centralization and minimizing the risks related to different laboratory procedures and the management of a high number of samples.

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样本跟踪工具:基于OpenArray技术和R脚本的基因组样本监测综合方法。
背景/目的:在专门设施中集中基因测序对于降低与诊断检测相关的成本至关重要。这些中心必须能够验证数据质量并确保样本完整性。本研究旨在开发一种跟踪ngs分析样本的方案,以防止错误和混淆,确保基因检测过程中适当的质量控制、准确性和可靠性。为此,采用基于OpenArrayTM技术对60个单核苷酸多态性(snp)进行基因分型的方案。方法:该方案最初在758个样本队列中进行测试,随后在100个样本队列中进行验证。此外,通过对另外100个样品进行模拟测试,评估了其准确检测相同和不同样品的能力。结果:共有55个探针的通过率≥90%,并通过专门开发的R工具进行了样本匹配过程。SNP面板的随机匹配概率为3.29 × 10-15,证明其适用于有效跟踪样品并快速识别分析过程中的任何错误或混淆。结论:OpenArrayTM技术具有成本效益高、分析速度快、判别能力强等特点,是样品跟踪的理想工具。总之,该方法为促进实验室集中化和最大限度地降低与不同实验室程序和大量样品管理相关的风险提供了有价值的示例。
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来源期刊
Diagnostics
Diagnostics Biochemistry, Genetics and Molecular Biology-Clinical Biochemistry
CiteScore
4.70
自引率
8.30%
发文量
2699
审稿时长
19.64 days
期刊介绍: Diagnostics (ISSN 2075-4418) is an international scholarly open access journal on medical diagnostics. It publishes original research articles, reviews, communications and short notes on the research and development of medical diagnostics. There is no restriction on the length of the papers. Our aim is to encourage scientists to publish their experimental and theoretical research in as much detail as possible. Full experimental and/or methodological details must be provided for research articles.
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