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dc.contributor.authorEslami, Mohammed
dc.contributor.authorBorujeni, Amin Espah
dc.contributor.authorEramian, Hamed
dc.contributor.authorWeston, Mark
dc.contributor.authorZheng, George
dc.contributor.authorUrrutia, Joshua
dc.contributor.authorCorbet, Carolyn
dc.contributor.authorBecker, Diveena
dc.contributor.authorMaschhoff, Paul
dc.contributor.authorClowers, Katie
dc.contributor.authorCristofaro, Alexander
dc.contributor.authorHosseini, Hamid Doost
dc.contributor.authorGordon, D Benjamin
dc.contributor.authorDorfan, Yuval
dc.contributor.authorSinger, Jedediah
dc.contributor.authorVaughn, Matthew
dc.contributor.authorGaffney, Niall
dc.contributor.authorFonner, John
dc.contributor.authorStubbs, Joe
dc.contributor.authorVoigt, Christopher A
dc.contributor.authorYeung, Enoch
dc.date.accessioned2023-02-07T17:43:14Z
dc.date.available2023-02-07T17:43:14Z
dc.date.issued2022
dc.identifier.urihttps://hdl.handle.net/1721.1/147936
dc.description.abstract<jats:title>Abstract</jats:title> <jats:sec> <jats:title>Motivation</jats:title> <jats:p>Applications in synthetic and systems biology can benefit from measuring whole-cell response to biochemical perturbations. Execution of experiments to cover all possible combinations of perturbations is infeasible. In this paper, we present the host response model (HRM), a machine learning approach that maps response of single perturbations to transcriptional response of the combination of perturbations.</jats:p> </jats:sec> <jats:sec> <jats:title>Results</jats:title> <jats:p>The HRM combines high-throughput sequencing with machine learning to infer links between experimental context, prior knowledge of cell regulatory networks, and RNASeq data to predict a gene’s dysregulation. We find that the HRM can predict the directionality of dysregulation to a combination of inducers with an accuracy of &amp;gt;90% using data from single inducers. We further find that the use of prior, known cell regulatory networks doubles the predictive performance of the HRM (an R2 from 0.3 to 0.65). The model was validated in two organisms, Escherichia coli and Bacillus subtilis, using new experiments conducted after training. Finally, while the HRM is trained with gene expression data, the direct prediction of differential expression makes it possible to also conduct enrichment analyses using its predictions. We show that the HRM can accurately classify &amp;gt;95% of the pathway regulations. The HRM reduces the number of RNASeq experiments needed as responses can be tested in silico prior to the experiment.</jats:p> </jats:sec> <jats:sec> <jats:title>Availability and implementation</jats:title> <jats:p>The HRM software and tutorial are available at https://github.com/sd2e/CDM and the configurable differential expression analysis tools and tutorials are available at https://github.com/SD2E/omics_tools.</jats:p> </jats:sec> <jats:sec> <jats:title>Supplementary information</jats:title> <jats:p>Supplementary data are available at Bioinformatics online.</jats:p> </jats:sec>en_US
dc.language.isoen
dc.publisherOxford University Press (OUP)en_US
dc.relation.isversionof10.1093/BIOINFORMATICS/BTAB676en_US
dc.rightsCreative Commons Attribution-Noncommercial-Share Alikeen_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/4.0/en_US
dc.sourcebioRxiven_US
dc.titlePrediction of whole-cell transcriptional response with machine learningen_US
dc.typeArticleen_US
dc.identifier.citationEslami, Mohammed, Borujeni, Amin Espah, Eramian, Hamed, Weston, Mark, Zheng, George et al. 2022. "Prediction of whole-cell transcriptional response with machine learning." Bioinformatics, 38 (2).
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biological Engineeringen_US
dc.relation.journalBioinformaticsen_US
dc.eprint.versionOriginal manuscripten_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/NonPeerRevieweden_US
dc.date.updated2023-02-07T17:29:40Z
dspace.orderedauthorsEslami, M; Borujeni, AE; Eramian, H; Weston, M; Zheng, G; Urrutia, J; Corbet, C; Becker, D; Maschhoff, P; Clowers, K; Cristofaro, A; Hosseini, HD; Gordon, DB; Dorfan, Y; Singer, J; Vaughn, M; Gaffney, N; Fonner, J; Stubbs, J; Voigt, CA; Yeung, Een_US
dspace.date.submission2023-02-07T17:29:42Z
mit.journal.volume38en_US
mit.journal.issue2en_US
mit.licenseOPEN_ACCESS_POLICY
mit.metadata.statusAuthority Work and Publication Information Neededen_US


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