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GaussianCpG: a Gaussian model for detection of CpG island in human genome sequences

机译:GaussianCpG:用于检测人类基因组序列中CpG岛的高斯模型

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摘要

BackgroundAs crucial markers in identifying biological elements and processes in mammalian genomes, CpG islands (CGI) play important roles in DNA methylation, gene regulation, epigenetic inheritance, gene mutation, chromosome inactivation and nuclesome retention. The generally accepted criteria of CGI rely on: (a) %G+C content is ≥ 50%, (b) the ratio of the observed CpG content and the expected CpG content is ≥ 0.6, and (c) the general length of CGI is greater than 200 nucleotides. Most existing computational methods for the prediction of CpG island are programmed on these rules. However, many experimentally verified CpG islands deviate from these artificial criteria. Experiments indicate that in many cases %G+C is < 50%, CpG obs/CpG exp varies, and the length of CGI ranges from eight nucleotides to a few thousand of nucleotides. It implies that CGI detection is not just a straightly statistical task and some unrevealed rules probably are hidden.
机译:背景技术CpG岛(CGI)作为识别哺乳动物基因组中生物元素和过程的关键标志物,在DNA甲基化,基因调控,表观遗传,基因突变,染色体失活和核小体保留中起着重要作用。 CGI的公认标准取决于:(a)G + C含量≥50%,(b)观察到的CpG含量与预期CpG含量之比≥0.6,以及(c)CGI的总长度大于200个核苷酸。在这些规则上可以编程用于预测CpG岛的大多数现有计算方法。但是,许多经过实验验证的CpG岛均偏离了这些人工标准。实验表明,在许多情况下,%G + C <50%,CpG obs / CpG exp有所不同,CGI的长度从8个核苷酸到数千个核苷酸不等。这意味着CGI检测不仅是一项直接的统计任务,而且某些未公开的规则可能被隐藏了。

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