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Newborn Screening for Phenylketonuria: Machine Learning vs Clinicians

机译:苯丙酮尿症的新生儿筛查:机器学习与临床医生

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The metabolic disorders may hinder an infant's normal physical or mental development during the neonatal period. The metabolic diseases can be treated by effective therapies if the diseases are discovered in the early stages. Therefore, newborn screening program is essential to prevent neonatal from these damages. In the paper, a support vector machine (SVM) based algorithm is introduced in place of cut-off value decision to evaluate the analyte elevation raw data associated with Phenylketonuria. The data were obtained from tandem mass spectrometry (MS/MS) for newborns. In addition, a combined feature selection mechanism is proposed to compare with the cut-off scheme. By adapting the mechanism, the number of suspected cases is reduced substantially, it also handles the medical resources effectively and efficiently.
机译:在新生儿期间,代谢异常可能会阻碍婴儿的正常身体或智力发育。如果在早期发现代谢性疾病,则可以通过有效的疗法进行治疗。因此,新生儿筛查程序对于防止新生儿受到这些损害至关重要。在本文中,引入了基于支持向量机(SVM)的算法来代替临界值决策,以评估与苯丙酮尿症相关的分析物海拔原始数据。数据是从新生儿串联质谱(MS / MS)获得的。此外,提出了一种组合特征选择机制,以与截止方案进行比较。通过调整机制,大大减少了疑似病例的数量,也有效地处理了医疗资源。

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