CancerInSilico: An R/Bioconductor package for combining mathematical and statistical modeling to simulate time course bulk and single cell gene expression data in cancer

dc.contributor.authorSherman, Thomas D.
dc.contributor.authorKagohara, Luciane T.
dc.contributor.authorCao, Raymon
dc.contributor.authorCheng, Raymond
dc.contributor.authorSatriano, Matthew
dc.contributor.authorConsidine, Michael
dc.contributor.authorKrigsfeld, Gabriel
dc.contributor.authorRanaweera, Ruchira
dc.contributor.authorTang, Yong
dc.contributor.authorJablonski, Sandra A.
dc.contributor.authorStein-O'Brien, Genevieve
dc.contributor.authorGaykalova, Daria A.
dc.contributor.authorWeiner, Louis M.
dc.contributor.authorChung, Christine H.
dc.contributor.authorFertig, Elana J.
dc.date.accessioned2026-05-08T20:00:40Z
dc.date.available2026-05-08T20:00:40Z
dc.date.issued2019-04-19
dc.description© 2019 Sherman et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
dc.description.abstractBioinformatics techniques to analyze time course bulk and single cell omics data are advancing. The absence of a known ground truth of the dynamics of molecular changes challenges benchmarking their performance on real data. Realistic simulated time-course datasets are essential to assess the performance of time course bioinformatics algorithms. We develop an R/Bioconductor package, CancerInSilico, to simulate bulk and single cell transcriptional data from a known ground truth obtained from mathematical models of cellular systems. This package contains a general R infrastructure for running cell-based models and simulating gene expression data based on the model states. We show how to use this package to simulate a gene expression data set and consequently benchmark analysis methods on this data set with a known ground truth. The package is freely available via Bioconductor: http://bioconductor.org/packages/CancerInSilico/
dc.description.sponsorshipNIH, CA177669 || NIH, CA006973 || NIH, CA212007 || NIH, CA50633 || NIH, CA51008 || NIH, DE017982 || SPORE, DE019032 || The Cleveland Foundation, Helen Masenhimer Fellowship || John Hopkins University, Catalyst Grant || John Hopkins University, Discovery Grant || John Hopkins School of Medicine, Synergy Award || Chan Zuckerberg Initiative DAF, 2018-183444.
dc.identifier.urihttps://doi.org/10.1371/journal.pcbi.1006935
dc.identifier.urihttps://hdl.handle.net/10012/23282
dc.language.isoen
dc.publisherPublic Library of Science
dc.relation.ispartofseriesPLoS Computational Biology; 14(4); e1006935
dc.relation.urihttps://github.com/FertigLab/CancerInSilico-Figures
dc.rightsAttribution 4.0 Internationalen
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subjectcancers and neoplasms
dc.subjectgene expression
dc.subjectsimulation and modeling
dc.subjectmathematical models
dc.subjectstatistical models
dc.subjectbioinformatics
dc.subjectcell cycle and cell division
dc.subjectsoftware tools
dc.titleCancerInSilico: An R/Bioconductor package for combining mathematical and statistical modeling to simulate time course bulk and single cell gene expression data in cancer
dc.typeArticle
dcterms.bibliographicCitationSherman TD, Kagohara LT, Cao R, Cheng R, Satriano M, Considine M, et al. (2018) CancerInSilico: An R/Bioconductor package for combining mathematical and statistical modeling to simulate time course bulk and single cell gene expression data in cancer. PLoS Comput Biol 14(4): e1006935. https://doi.org/10.1371/journal.pcbi.1006935
uws.contributor.affiliation1Faculty of Mathematics
uws.contributor.affiliation2Applied Mathematics
uws.peerReviewStatusReviewed
uws.scholarLevelFaculty
uws.typeOfResourceTexten

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