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Venn-diaNet : venn diagram based network propagation analysis framework for comparing multiple biological experiments

DC Field Value Language
dc.contributor.authorHur, Benjamin-
dc.contributor.authorKang, Dongwon-
dc.contributor.authorLee, Sangseon-
dc.contributor.authorMoon, Ji Hwan-
dc.contributor.authorLee, Gung-
dc.contributor.authorKim, Sun-
dc.date.accessioned2020-04-01T02:00:40Z-
dc.date.available2020-04-01T11:10:55Z-
dc.date.issued2019-12-27-
dc.identifier.citationBMC Bioinformatics, 20(Suppl 23):667ko_KR
dc.identifier.issn1471-2105-
dc.identifier.uri10.1186/s12859-019-3302-7-
dc.identifier.urihttps://hdl.handle.net/10371/164887-
dc.description.abstractBackground
The main research topic in this paper is how to compare multiple biological experiments using transcriptome data, where each experiment is measured and designed to compare control and treated samples. Comparison of multiple biological experiments is usually performed in terms of the number of DEGs in an arbitrary combination of biological experiments. This process is usually facilitated with Venn diagram but there are several issues when Venn diagram is used to compare and analyze multiple experiments in terms of DEGs. First, current Venn diagram tools do not provide systematic analysis to prioritize genes. Because that current tools generally do not fully focus to prioritize genes, genes that are located in the segments in the Venn diagram (especially, intersection) is usually difficult to rank. Second, elucidating the phenotypic difference only with the lists of DEGs and expression values is challenging when the experimental designs have the combination of treatments. Experiment designs that aim to find the synergistic effect of the combination of treatments are very difficult to find without an informative system.

Results
We introduce Venn-diaNet, a Venn diagram based analysis framework that uses network propagation upon protein-protein interaction network to prioritizes genes from experiments that have multiple DEG lists. We suggest that the two issues can be effectively handled by ranking or prioritizing genes with segments of a Venn diagram. The user can easily compare multiple DEG lists with gene rankings, which is easy to understand and also can be coupled with additional analysis for their purposes. Our system provides a web-based interface to select seed genes in any of areas in a Venn diagram and then perform network propagation analysis to measure the influence of the selected seed genes in terms of ranked list of DEGs.

Conclusions
We suggest that our system can logically guide to select seed genes without additional prior knowledge that makes us free from the seed selection of network propagation issues. We showed that Venn-diaNet can reproduce the research findings reported in the original papers that have experiments that compare two, three and eight experiments. Venn-diaNet is freely available at: http://biohealth.snu.ac.kr/software/venndianet
ko_KR
dc.description.sponsorshipThis publication has been funded by (i) Next-Generation Information Computing Development Program through the National Research Foundation of Korea (NRF) the Ministry of Science ICT (MSIT) (No.NRF-2017M3C4A7065887), (ii) The Collaborative Genome Program for Fostering New Post-Genome Industry of the National Research Foundation (NRF), the Ministry of Science and ICT (MSIT) (No.NRF2014M3C9A3063541), and (iii) a grant of the Korea Health Technology R&D Project through the Korea
Health Industry Development Institute (KHIDI) the Ministry of Health & Welfare, Republic of Korea (Grant number: HI15C3224).
ko_KR
dc.language.isoenko_KR
dc.publisherBMCko_KR
dc.subjectVenn diagram-
dc.subjectDifferentially expressed genes-
dc.subjectNetwork propagation-
dc.subjectGene prioritization-
dc.titleVenn-diaNet : venn diagram based network propagation analysis framework for comparing multiple biological experimentsko_KR
dc.typeArticleko_KR
dc.contributor.AlternativeAuthor강동원-
dc.contributor.AlternativeAuthor이상선-
dc.contributor.AlternativeAuthor문지환-
dc.contributor.AlternativeAuthor김선-
dc.citation.journaltitleBMC Bioinformaticsko_KR
dc.language.rfc3066en-
dc.rights.holderThe Author(s)-
dc.date.updated2019-12-29T04:11:56Z-
dc.citation.numberSuppl 23ko_KR
dc.citation.startpage667ko_KR
dc.citation.volume20ko_KR
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