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Phylogenetic Analysis of Mass Spectrometry or Gene Array Data for the Diagnosis of Physiological Conditions

机译:质谱或基因阵列数据的系统发育分析,用于诊断生理状况

摘要

A universal data-mining platform capable of analyzing mass spectrometry (MS) serum proteomic profiles and/or gene array data to produce biologically meaningful classification; i.e., group together biologically related specimens into clades. This platform utilizes the principles of phylogenetics, such as parsimony, to reveal susceptibility to cancer development (or other physiological or pathophysiological conditions), diagnosis and typing of cancer, identifying stages of cancer, as well as post-treatment evaluation. To place specimens into their corresponding clade(s), the invention utilizes two algorithms: a new data-mining parsing algorithm, and a publicly available phylogenetic algorithm (MIX). By outgroup comparison (i.e., using a normal set as the standard reference), the parsing algorithm identifies under and/or overexpressed gene values or in the case of sera, (i) novel or (ii) vanished MS peaks, and peaks signifying (iii) up or (iv) down regulated proteins, and scores the variations as either derived (do not exit in the outgroup set) or ancestral (exist in the outgroup set); the derived is given a score of “1”, and the ancestral a score of “0”—these are called the polarized values. Furthermore, the shared derived characters that it identifies are potential biomarkers for cancers and other conditions and their subclasses.
机译:一个通用的数据挖掘平台,能够分析质谱(MS)血清蛋白质组学特征和/或基因阵列数据,以产生生物学上有意义的分类;即,将生物学相关的标本归类为进化枝。该平台利用系统进化学的原理(例如简约性)来揭示对癌症发展(或其他生理或病理生理状况),癌症的诊断和分型,确定癌症的阶段以及治疗后评估的易感性。为了将标本放入它们对应的进化枝中,本发明利用两种算法:新的数据挖掘解析算法和公开可用的系统发生算法(MIX)。通过组外比较(即,使用正常集作为标准参考),解析算法可以识别出低于和/或过表达的基因值,或者在血清的情况下,(i)新的或(ii)消失的MS峰,并且峰表示( iii)上调或(iv)下调的蛋白质,并对变异进行评分,得出的变异是衍生的(不存在于外群中)或祖先的(存在于外群中);派生的分数为“ 1”,祖先的分数为“ 0”,这些被称为极化值。此外,它识别出的共有衍生特征是癌症和其他疾病及其亚类的潜在生物标记。

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