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Hamming Distance as a Concept in DNA Molecular Recognition

机译:汉明距离作为DNA分子识别中的一个概念

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摘要

DNA microarrays constitute an in vitro example system of a highly crowded molecular recognition environment. Although they are widely applied in many biological applications, some of the basic mechanisms of the hybridization processes of DNA remain poorly understood. On a microarray, cross-hybridization arises from similarities of sequences that may introduce errors during the transmission of information. Experimentally, we determine an appropriate distance, called minimum Hamming distance, in which the sequences of a set differ. By applying an algorithm based on a graph-theoretical method, we find large orthogonal sets of sequences that are sufficiently different not to exhibit any cross-hybridization. To create such a set, we first derive an analytical solution for the number of sequences that include at least four guanines in a row for a given sequence length and eliminate them from the list of candidate sequences. We experimentally confirm the orthogonality of the largest possible set with a size of 23 for the length of 7. We anticipate our work to be a starting point toward the study ofsignal propagation in highly competitive environments, besides itsobvious application in DNA high throughput experiments.
机译:DNA微阵列构成了高度拥挤的分子识别环境的体外示例系统。尽管它们广泛地应用于许多生物学应用中,但对DNA杂交过程的一些基本机制仍然知之甚少。在微阵列上,交叉杂交源自序列的相似性,这些相似性可能在信息传输过程中引入错误。在实验上,我们确定一个合适的距离,称为最小汉明距离,其中一组序列不同。通过应用基于图论方法的算法,我们发现了大的正交序列集,这些序列的差异足够大,不会表现出任何交叉杂交。为了创建这样的集合,我们首先导出对于给定序列长度连续包含至少四个鸟嘌呤的序列数量的解析解,并将其从候选序列列表中消除。我们通过实验确定了长度为7的最大可能集(大小为23)的正交性。我们预计我们的工作将成为研究λ的起点。信号在竞争激烈的环境中传播在DNA高通量实验中有明显的应用。

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