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dc.contributor.authorDeJesus, Michael A.
dc.contributor.authorNambi, Subhalaxmi
dc.contributor.authorSmith, Clare M.
dc.contributor.authorBaker, Richard E.
dc.contributor.authorSassetti, Christopher M.
dc.contributor.authorIoerger, Thomas R.
dc.date2022-08-11T08:09:21.000
dc.date.accessioned2022-08-23T16:27:09Z
dc.date.available2022-08-23T16:27:09Z
dc.date.issued2017-02-22
dc.date.submitted2017-05-25
dc.identifier.citationNucleic Acids Res. 2017 Feb 22. doi: 10.1093/nar/gkx128. <a href="https://doi.org/10.1093/nar/gkx128">Link to article on publisher's site</a>
dc.identifier.issn0305-1048 (Linking)
dc.identifier.doi10.1093/nar/gkx128
dc.identifier.pmid28334803
dc.identifier.urihttp://hdl.handle.net/20.500.14038/36719
dc.description.abstractTn-Seq is an experimental method for probing the functions of genes through construction of complex random transposon insertion libraries and quantification of each mutant's abundance using next-generation sequencing. An important emerging application of Tn-Seq is for identifying genetic interactions, which involves comparing Tn mutant libraries generated in different genetic backgrounds (e.g. wild-type strain versus knockout strain). Several analytical methods have been proposed for analyzing Tn-Seq data to identify genetic interactions, including estimating relative fitness ratios and fitting a generalized linear model. However, these have limitations which necessitate an improved approach. We present a hierarchical Bayesian method for identifying genetic interactions through quantifying the statistical significance of changes in enrichment. The analysis involves a four-way comparison of insertion counts across datasets to identify transposon mutants that differentially affect bacterial fitness depending on genetic background. Our approach was applied to Tn-Seq libraries made in isogenic strains of Mycobacterium tuberculosis lacking three different genes of unknown function previously shown to be necessary for optimal fitness during infection. By analyzing the libraries subjected to selection in mice, we were able to distinguish several distinct classes of genetic interactions for each target gene that shed light on their functions and roles during infection.
dc.language.isoen_US
dc.relation<a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=28334803&dopt=Abstract">Link to Article in PubMed</a>
dc.relation.urlhttps://doi.org/10.1093/nar/gkx128
dc.rights© The Author(s) 2017. Published by Oxford University Press on behalf of Nucleic Acids Research.
dc.rights.urihttp://creativecommons.org/licenses/by-nc/4.0/
dc.subjectgenes
dc.subjectlibraries
dc.subjectdna transposons
dc.subjectgene interaction
dc.subjectdatasets
dc.subjectBiochemistry
dc.subjectCellular and Molecular Physiology
dc.subjectComputational Biology
dc.subjectMicrobiology
dc.subjectMolecular Biology
dc.titleStatistical analysis of genetic interactions in Tn-Seq data
dc.typeJournal Article
dc.source.journaltitleNucleic acids research
dc.identifier.legacyfulltexthttps://escholarship.umassmed.edu/cgi/viewcontent.cgi?article=1086&amp;context=metnet_pubs&amp;unstamped=1
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/metnet_pubs/87
dc.identifier.contextkey10212152
refterms.dateFOA2022-08-23T16:27:09Z
html.description.abstract<p>Tn-Seq is an experimental method for probing the functions of genes through construction of complex random transposon insertion libraries and quantification of each mutant's abundance using next-generation sequencing. An important emerging application of Tn-Seq is for identifying genetic interactions, which involves comparing Tn mutant libraries generated in different genetic backgrounds (e.g. wild-type strain versus knockout strain). Several analytical methods have been proposed for analyzing Tn-Seq data to identify genetic interactions, including estimating relative fitness ratios and fitting a generalized linear model. However, these have limitations which necessitate an improved approach. We present a hierarchical Bayesian method for identifying genetic interactions through quantifying the statistical significance of changes in enrichment. The analysis involves a four-way comparison of insertion counts across datasets to identify transposon mutants that differentially affect bacterial fitness depending on genetic background. Our approach was applied to Tn-Seq libraries made in isogenic strains of Mycobacterium tuberculosis lacking three different genes of unknown function previously shown to be necessary for optimal fitness during infection. By analyzing the libraries subjected to selection in mice, we were able to distinguish several distinct classes of genetic interactions for each target gene that shed light on their functions and roles during infection.</p>
dc.identifier.submissionpathmetnet_pubs/87
dc.contributor.departmentDepartment of Microbiology and Physiological Systems


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© The Author(s) 2017. Published by Oxford University Press on behalf of Nucleic Acids Research.
Except where otherwise noted, this item's license is described as © The Author(s) 2017. Published by Oxford University Press on behalf of Nucleic Acids Research.