C3: connect separate connected components to form a succinct disease module

Precise disease module is conducive to understanding the molecular mechanism of disease causation and identifying drug targets. However, due to the fragmentization of disease module in incomplete human interactome, how to determine connectivity pattern and detect a complete neighbourhood of disease...

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Veröffentlicht in:BMC bioinformatics 2020-10, Vol.21 (1), p.1-433, Article 433
Hauptverfasser: Wang, Bingbo, Hu, Jie, Wang, Yajun, Zhang, Chenxing, Zhou, Yuanjun, Yu, Liang, Guo, Xingli, Gao, Lin, Chen, Yunru
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Sprache:eng
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Zusammenfassung:Precise disease module is conducive to understanding the molecular mechanism of disease causation and identifying drug targets. However, due to the fragmentization of disease module in incomplete human interactome, how to determine connectivity pattern and detect a complete neighbourhood of disease based on this is still an open question. In this paper, we perform exploratory analysis leading to an important observation that through a few intermediate nodes, most separate connected components formed by disease-associated proteins can be effectively connected and eventually form a complete disease module. And based on the topological properties of these intermediate nodes, we propose a connect separate connected components (C3) method to detect a succinct disease module by introducing a relatively small number of intermediate nodes, which allows us to obtain more pure disease module than other methods. Then we apply C3 across a large corpus of diseases to validate this connectivity pattern of disease module. Furthermore, the connectivity of the perturbed genes in multi-omics data such as The Cancer Genome Atlas also fits this pattern. C3 tool is not only useful in detecting a clearly-defined connected disease neighbourhood of 299 diseases and cancer with multi-omics data, but also helpful in better understanding the interconnection of phenotypically related genes in different omics data and studying complex pathological processes.
ISSN:1471-2105
1471-2105
DOI:10.1186/s12859-020-03769-y