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BPDA2d—a 2D global optimization-based Bayesian peptide detection algorithm for liquid chromatograph–mass spectrometry

机译:BPDA2d-基于二维全局优化的贝叶斯肽检测算法用于液相色谱-质谱

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摘要

>Motivation: Peptide detection is a crucial step in mass spectrometry (MS) based proteomics. Most existing algorithms are based upon greedy isotope template matching and thus may be prone to error propagation and ineffective to detect overlapping peptides. In addition, existing algorithms usually work at different charge states separately, isolating useful information that can be drawn from other charge states, which may lead to poor detection of low abundance peptides.>Results: BPDA2d models spectra as a mixture of candidate peptide signals and systematically evaluates all possible combinations of possible peptide candidates to interpret the given spectra. For each candidate, BPDA2d takes into account its elution profile, charge state distribution and isotope pattern, and it combines all evidence to infer the candidate's signal and existence probability. By piecing all evidence together—especially by deriving information across charge states—low abundance peptides can be better identified and peptide detection rates can be improved. Instead of local template matching, BPDA2d performs global optimization for all candidates and systematically optimizes their signals. Since BPDA2d looks for the optimal among all possible interpretations of the given spectra, it has the capability in handling complex spectra where features overlap. BPDA2d estimates the posterior existence probability of detected peptides, which can be directly used for probability-based evaluation in subsequent processing steps. Our experiments indicate that BPDA2d outperforms state-of-the-art detection methods on both simulated data and real liquid chromatography–mass spectrometry data, according to sensitivity and detection accuracy.>Availability: The BPDA2d software package is available at >Contact: ; >Supplementary information: are available at Bioinformatics online.
机译:>动机:肽段检测是基于质谱(MS)的蛋白质组学中的关键步骤。现有的大多数算法都基于贪婪的同位素模板匹配,因此可能易于错误传播并且无法有效检测重叠的肽段。此外,现有的算法通常分别在不同的电荷状态下工作,从而从其他电荷状态中分离出有用的信息,这可能导致对低丰度多肽的检测效果很差。>结果:BPDA2d将光谱建模为候选肽信号的混合,并系统评估可能的候选肽的所有组合,以解释给定的光谱。对于每个候选物,BPDA2d考虑到其洗脱曲线,电荷状态分布和同位素模式,并结合所有证据来推断该候选物的信号和存在概率。通过将所有证据拼凑在一起(尤其是通过跨电荷状态获取信息),可以更好地识别低丰度多肽,并可以提高多肽检测率。 BPDA2d代替全局模板匹配,而是对所有候选对象执行全局优化,并系统地优化其信号。由于BPDA2d会在给定光谱的所有可能解释中寻求最佳,因此它具有处理特征重叠的复杂光谱的能力。 BPDA2d估计检测到的肽的后验存在概率,可以将其直接用于后续处理步骤中基于概率的评估。我们的实验表明,根据灵敏度和检测精度,BPDA2d在模拟数据和实际液相色谱-质谱分析数据上均优于最新的检测方法。>可用性:在>联系人:; >补充信息:可在线访问生物信息学。

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