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A multi-dimensional evidence-based candidate gene prioritization approach for complex diseases-schizophrenia as a case

机译:基于多维证据的复杂疾病-精神分裂症候选基因优先排序方法

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摘要

MOTIVATION: During the past decade, we have seen an exponential growth of vast amounts of genetic data generated for complex disease studies. Currently, across a variety of complex biological problems, there is a strong trend towards the integration of data from multiple sources. So far, candidate gene prioritization approaches have been designed for specific purposes, by utilizing only some of the available sources of genetic studies, or by using a simple weight scheme. Specifically to psychiatric disorders, there has been no prioritization approach that fully utilizes all major sources of experimental data. RESULTS: Here we present a multi-dimensional evidence-based candidate gene prioritization approach for complex diseases and demonstrate it in schizophrenia. In this approach, we first collect and curate genetic studies for schizophrenia from four major categories: association studies, linkage analyses, gene expression and literature search. Genes in these data sets are initially scored by category-specific scoring methods. Then, an optimal weight matrix is searched by a two-step procedure (core genes and unbiased P-values in independent genome-wide association studies). Finally, genes are prioritized by their combined scores using the optimal weight matrix. Our evaluation suggests this approach generates prioritized candidate genes that are promising for further analysis or replication. The approach can be applied to other complex diseases. AVAILABILITY: The collected data, prioritized candidate genes, and gene prioritization tools are freely available at http://bioinfo.mc.vanderbilt.edu/SZGR/.
机译:动因:在过去十年中,我们已经看到为复杂疾病研究生成的大量遗传数据呈指数增长。当前,在各种复杂的生物学问题中,有一个趋势是要整合来自多个来源的数据。到目前为止,已经通过仅利用一些遗传研究的可用资源或使用简单的权重方案为特定目的设计了候选基因优先排序方法。专门针对精神疾病,没有一种优先排序方法可以充分利用所有主要的实验数据来源。结果:在这里,我们提出了一种基于多维证据的复杂疾病候选基因优先排序方法,并在精神分裂症中进行了证明。在这种方法中,我们首先从四个主要类别收集和策划针对精神分裂症的遗传研究:关联研究,连锁分析,基因表达和文献检索。这些数据集中的基因最初是通过类别特定的评分方法评分的。然后,通过两步过程(在独立的全基因组关联研究中,核心基因和无偏P值)搜索最佳权重矩阵。最后,使用最佳权重矩阵通过基因的综合得分对基因进行优先排序。我们的评估表明,这种方法会产生优先的候选基因,有望用于进一步的分析或复制。该方法可以应用于其他复杂疾病。可用性:可以从http://bioinfo.mc.vanderbilt.edu/SZGR/免费获得所收集的数据,优先候选基因和基因优先工具。

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