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Genetic Programming for Measuring Peptide Detectability

机译:遗传程序用于测量肽的可检测性

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The biomarker discovery process usually produces a long list of candidates, which need to be verified. The verification of protein biomarkers from mass spectrometry data can be done through measuring the detection probability from the mass spectrometer (Peptide detection). However, the limited size of the experimental data and lack of a universal quantitative method make the identification of these pep-tides challenging. In this paper, genetic programming (GP) is proposed to measure the detection of the peptides in the mass spectrometer. This is done through measuring the physicochemical chemicals of the peptides and selecting the high responding peptides. The proposed method performs both feature selection and classification, where feature selection is adopted to determine the important physicochemical properties required for the prediction. The proposed GP method is tested on two different yeast data sets with increasing complexity. It outperforms five other state-of-the-art classification algorithms. The results also show that GP outperforms two conventional feature selection methods, namely, Chi Square and Information Gain Ratio.
机译:生物标志物发现过程通常会产生一长串候选者,需要对其进行验证。可以通过测量质谱仪(肽段检测)的检测概率来完成从质谱数据中对蛋白质生物标志物的验证。然而,实验数据的有限性和缺乏通用的定量方法使得鉴定这些肽具有挑战性。在本文中,提出了遗传程序(GP)来测量质谱仪中肽段的检测。这是通过测量肽的理化化学成分并选择高响应肽来完成的。所提出的方法既执行特征选择又进行分类,其中特征选择用于确定预测所需的重要理化性质。所提出的GP方法在两个不同的酵母数据集上进行了测试,且复杂度不断提高。它优于其他五种最新的分类算法。结果还表明,GP胜过两种传统的特征选择方法,即Chi Square和Information Gain Ratio。

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