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Variable locus length in the human genome leads to ascertainment bias in functional inference for non-coding elements

机译:人类基因组中可变的基因座长度导致非编码元件功能推断的确定偏差

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摘要

Motivation: Several functional gene annotation databases have been developed in the recent years, and are widely used to infer the biological function of gene sets, by scrutinizing the attributes that appear over- and underrepresented. However, this strategy is not directly applicable to the study of non-coding DNA, as the non-coding sequence span varies greatly among different gene loci in the human genome and longer loci have a higher likelihood of being selected purely by chance. Therefore, conclusions involving the function of non-coding elements that are drawn based on the annotation of neighboring genes are often biased. We assessed the systematic bias in several particular Gene Ontology (GO) categories using the standard hypergeometric test, by randomly sampling non-coding elements from the human genome and inferring their function based on the functional annotation of the closest genes. While no category is expected to occur significantly over- or underrepresented for a random selection of elements, categories such as ‘cell adhesion’, ‘nervous system development’ and ‘transcription factor activities’ appeared to be systematically overrepresented, while others such as ‘olfactory receptor activity’—underrepresented.
机译:动机:近年来已经开发了几个功能性基因注释数据库,并且通过仔细检查出现过高和过低表示的属性,它们被广泛用于推断基因组的生物学功能。但是,这种策略不能直接应用于非编码DNA的研究,因为人类基因组中不同基因位点之间的非编码序列跨度差异很大,而更长的位点纯属偶然地被选择的可能性更高。因此,涉及基于邻近基因的注释而得出的非编码元件功能的结论常常是有偏见的。我们使用标准的超几何学测试,通过从人类基因组中随机采样非编码元素并根据最近基因的功能注释推断其功能,来评估几种特定基因本体论(GO)类别中的系统偏见。尽管对于随机选择的元素,预计不会出现类别过多或不足的情况,但是诸如“细胞粘附”,“神经系统发育”和“转录因子活性”之类的类别似乎被系统地过度代表,而其他类别如“嗅觉”受体活性”-代表性不足。

著录项

  • 作者

    Taher, Leila; Ovcharenko, Ivan;

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  • 年度 2009
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  • 原文格式 PDF
  • 正文语种 {"code":"en","name":"English","id":9}
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