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COMPETITIVE POPULATION NORMALIZATION FOR COMPARATIVE ANALYSIS OF NUCLEIC ACID SAMPLES

机译:核酸样本比较分析中的竞争人口标准化

摘要

Methods are disclosed that convert two or more complex nucleic acid samples into a single collection of normalized target molecules that can be used to compare the abundance of each of the targets in the original samples. Multiple RNA or DNA samples are uniquely tagged and pooled to create a sample mixture. A defined set of target within the sample mixture is converted to approximately equal amounts of nucleic acid by one of several methods employing primer extension with a set of target specific primers. The concentration of target specific primers is equal and limiting for all targets, therefore an appropriate number of primer extension cycles converts all targets to similar final concentrations of product nucleic acid. The different tags appended to the sample nucleic acids from each sample population unique. These different tags are used to generate RNA or DNA , molecules for analysis that derive form each of the input samples. The disclosed methods are primarily intended to enhance gene array analysis, however, any method used to compare multiple nucleic acid targets form different samples will benefit form the invention.
机译:公开了将两个或更多个复杂核酸样品转化为标准化靶分子的单个集合的方法,其可用于比较原始样品中每个靶的丰度。多个RNA或DNA样品被唯一标记并合并以创建样品混合物。通过采用引物延伸和一组靶特异性引物的几种方法中的一种,将样品混合物中的一组确定的靶标转化为大约相等量的核酸。靶标特异性引物的浓度相等且限制所有靶标,因此适当数量的引物延伸循环可将所有靶标转化为相似的最终核酸产物浓度。来自每个样本群体的附加到样本核酸的不同标签是唯一的。这些不同的标签用于生成RNA或DNA分子,以进行分析,这些分子是从每个输入样本中衍生出来的。所公开的方法主要旨在增强基因阵列分析,但是,用于比较来自不同样品的多个核酸靶标的任何方法将从本发明中受益。

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