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Ontological Discovery Environment: a system for integrating gene-phenotype associations.

机译:本体发现环境:用于整合基因表型关联的系统。

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The wealth of genomic technologies has enabled biologists to rapidly ascribe phenotypic characters to biological substrates. Central to effective biological investigation is the operational definition of the process under investigation. We propose an elucidation of categories of biological characters, including disease relevant traits, based on natural endogenous processes and experimentally observed biological networks, pathways and systems rather than on externally manifested constructs and current semantics such as disease names and processes. The Ontological Discovery Environment (ODE) is an Internet accessible resource for the storage, sharing, retrieval and analysis of phenotype-centered genomic data sets across species and experimental model systems. Any type of data set representing gene-phenotype relationships, such quantitative trait loci (QTL) positional candidates, literature reviews, microarray experiments, ontological or even meta-data, may serve as inputs. To demonstrate a use case leveraging the homology capabilities of ODE and its ability to synthesize diverse data sets, we conducted an analysis of genomic studies related to alcoholism. The core of ODE's gene set similarity, distance and hierarchical analysis is the creation of a bipartite network of gene-phenotype relations, a unique discrete graph approach to analysis that enables set-set matching of non-referential data. Gene sets are annotated with several levels of metadata, including community ontologies, while gene set translations compare models across species. Computationally derived gene sets are integrated into hierarchical trees based on gene-derived phenotype interdependencies. Automated set identifications are augmented by statistical tools which enable users to interpret the confidence of modeled results. This approach allows data integration and hypothesis discovery across multiple experimental contexts, regardless of the face similarity and semantic annotation of the experimental systems or species domain.
机译:丰富的基因组技术使生物学家能够迅速将表型特征归因于生物底物。有效生物学调查的核心是所调查过程的操作定义。我们建议根据自然内生过程和实验观察到的生物学网络,途径和系统,而不是基于外部表现的结构和当前语义(例如疾病名称和过程),阐明生物特征的类别,包括与疾病相关的性状。本体发现环境(ODE)是Internet上可访问的资源,用于跨物种和实验模型系统存储,共享,检索和分析以表型为中心的基因组数据集。代表基因表型关系的任何类型的数据集,例如定量性状基因位点(QTL)定位候选物,文献综述,微阵列实验,本体论甚至元数据,都可以用作输入。为了演示利用ODE的同源性及其综合各种数据集的能力的用例,我们对与酗酒有关的基因组研究进行了分析。 ODE基因组相似性,距离和层次分析的核心是创建基因表型关系的双向网络,这是一种独特的离散图分析方法,可以对非参考数据进行组集匹配。基因集带有多个级别的元数据,包括社区本体,被注释,而基因集翻译则比较了跨物种的模型。基于基因衍生的表型相互依赖性,将计算得出的基因集整合到层次树中。统计工具增强了自动集合识别的能力,使用户能够解释建模结果的置信度。这种方法允许跨多个实验上下文进行数据集成和发现假设,而与实验系统或物种域的面孔相似性和语义注释无关。

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