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Predicting demographic group structures based on DNA sequence data

机译:基于DNA序列数据预测人口群体结构

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The ability to infer relationships between groups of sequences, either by searching for their evolutionary history or by comparing their sequence similarity, can be a crucial step in hypothesis testing. Interpreting relationships of human immunodeficiency virus type 1 (HIV-1) sequences can be challenging because of their rapidly evolving genotnes, but it may also lead to a better understanding of the underlying biology. Several studies have focused on the evolution of HIV-1, but there is little information to link sequence similarities and evolutionary histories of HIV-1 to the epidemiological information of the infected individual. Our goal was to correlate patterns of HIV-1 genetic diversity with epidemiological information, including risk and demographic factors. These correlations were then used to predict epidemiological information through analyzing short stretches of HIV-1 sequence. Using standard phylogenetic and phenetic techniques on 100 HIV-1 subtype B sequences, we were able to show some correlation between the viral sequences and the geographic area of infection and the risk of men who engage in sex with men. To help identify more subtle relationships between the viral sequences, the method of multidimensional scaling (MDS) was performed. That method identified statistically significant correlations between the viral sequences and the risk factors of men who engage in sex with men and individuals who engage in sex with injection drug users or use injection drugs themselves. Using tree construction, MDS, and newly developed likelihood assignment methods on the original 100 samples we sequenced, and also on a set of blinded samples, we were able to predict demographic/risk group membership at a rate statistically better than by chance alone. Such methods may make it possible to identify viral variants belonging to specific demographic groups by examining only a small portion of the HIV-1 genome. Such predictions of demographic epidemiology based on sequence information may become valuable in assigning different treatment regimens to infected individuals.
机译:通过搜索序列的进化历史或比较序列相似性来推断序列组之间关系的能力可能是假设检验的关键步骤。解释人类免疫缺陷病毒 1 型 (HIV-1) 序列的关系可能具有挑战性,因为它们的基因基快速进化,但它也可能导致对潜在生物学的更好理解。一些研究集中在HIV-1的进化上,但很少有信息将HIV-1的序列相似性和进化史与感染个体的流行病学信息联系起来。我们的目标是将HIV-1遗传多样性的模式与流行病学信息(包括风险和人口因素)相关联。然后,这些相关性用于通过分析HIV-1序列的短段来预测流行病学信息。在 100 个 HIV-1 亚型 B 序列上使用标准的系统发育和表型技术,我们能够显示病毒序列与感染地理区域之间的一些相关性以及男性与男性发生性关系的风险。为了帮助识别病毒序列之间更微妙的关系,进行了多维缩放(MDS)方法。该方法确定了病毒序列与与男性发生性关系的男性和与注射吸毒者发生性关系或自己使用注射毒品的个人的风险因素之间的统计学显着相关性。使用树构造、MDS 和新开发的可能性分配方法,对我们测序的原始 100 个样本以及一组盲法样本进行预测,我们能够以统计学上优于单纯偶然的比率预测人口统计学/风险组成员。这些方法可以通过仅检查HIV-1基因组的一小部分来识别属于特定人口群体的病毒变异。这种基于序列信息的人口流行病学预测在为感染者分配不同的治疗方案时可能变得很有价值。

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