Please use this identifier to cite or link to this item: http://hdl.handle.net/20.500.11861/7479
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dc.contributor.authorLo, Leung-Yauen_US
dc.contributor.authorWong, Man-Leungen_US
dc.contributor.authorLee, Kin-Hongen_US
dc.contributor.authorProf. LEUNG Kwong Saken_US
dc.date.accessioned2023-03-15T02:13:01Z-
dc.date.available2023-03-15T02:13:01Z-
dc.date.issued2015-
dc.identifier.citationPLoS ONE , 2015, 10(9), e0138596en_US
dc.identifier.urihttp://hdl.handle.net/20.500.11861/7479-
dc.description.abstractInferring the gene regulatory network (GRN) is crucial to understanding the working of the cell. Many computational methods attempt to infer the GRN from time series expression data, instead of through expensive and time-consuming experiments. However, existing methods make the convenient but unrealistic assumption of causal sufficiency, i.e. all the relevant factors in the causal network have been observed and there are no unobserved common cause. In principle, in the real world, it is impossible to be certain that all relevant factors or common causes have been observed, because some factors may not have been conceived of, and therefore are impossible to measure. In view of this, we have developed a novel algorithm named HCC-CLINDE to infer an GRN from time series data allowing the presence of hidden common cause(s). We assume there is a sparse causal graph (possibly with cycles) of interest, where the variables are continuous and each causal link has a delay (possibly more than one time step). A small but unknown number of variables are not observed. Each unobserved variable has only observed variables as children and parents, with at least two children, and the children are not linked to each other. Since it is difficult to obtain very long time series, our algorithm is also capable of utilizing multiple short time series, which is more realistic. To our knowledge, our algorithm is far less restrictive than previous works. We have performed extensive experiments using synthetic data on GRNs of size up to 100, with up to 10 hidden nodes. The results show that our algorithm can adequately recover the true causal GRN and is robust to slight deviation from Gaussian distribution in the error terms. We have also demonstrated the potential of our algorithm on small YEASTRACT subnetworks using limited real data.en_US
dc.language.isoenen_US
dc.relation.ispartofPLoS Oneen_US
dc.titleTime Delayed Causal Gene Regulatory Network Inference with Hidden Common Causesen_US
dc.typePeer Reviewed Journal Articleen_US
dc.identifier.doi10.1371/journal.pone.0138596-
item.fulltextNo Fulltext-
crisitem.author.deptDepartment of Applied Data Science-
Appears in Collections:Applied Data Science - Publication
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