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Newborn Screening for Phenylketonuria: Machine Learning vs Clinicians

机译:新生儿苯丙酮尿筛选: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:代谢障碍可能在新生儿期间妨碍婴儿的正常身体或精神发育。 如果在早期阶段发现疾病,可以通过有效疗法治疗代谢疾病。 因此,新生儿筛查计划对于防止新生儿免受这些损害至关重要。 在本文中,引入了一种基于支持向量机(SVM)的算法,代替截止值决定,以评估与苯丙酮尿尿尿的分析物升高原料数据。 数据从串联质谱(MS / MS)获得的新生儿。 另外,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,疑似病例的数量大幅度减少,它还有效且有效地处理医疗资源。

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