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dc.contributor.authorRachid Zaim, Samir
dc.contributor.authorKenost, Colleen
dc.contributor.authorBerghout, Joanne
dc.contributor.authorVitali, Francesca
dc.contributor.authorZhang, Helen Hao
dc.contributor.authorLussier, Yves A
dc.date.accessioned2019-08-22T19:31:12Z
dc.date.available2019-08-22T19:31:12Z
dc.date.issued2019-07-11
dc.identifier.citationZaim, S. R., Kenost, C., Berghout, J., Vitali, F., Zhang, H. H., & Lussier, Y. A. (2019). Evaluating single-subject study methods for personal transcriptomic interpretations to advance precision medicine. BMC medical genomics, 12(5), 96.en_US
dc.identifier.issn1755-8794
dc.identifier.pmid31296218
dc.identifier.doi10.1186/s12920-019-0513-8
dc.identifier.urihttp://hdl.handle.net/10150/633935
dc.description.abstractBackground Gene expression profiling has benefited medicine by providing clinically relevant insights at the molecular candidate and systems levels. However, to adopt a more precision' approach that integrates individual variability including omics data into risk assessments, diagnoses, and therapeutic decision making, whole transcriptome expression needs to be interpreted meaningfully for single subjects. We propose an all-against-one framework that uses biological replicates in isogenic conditions for testing differentially expressed genes (DEGs) in a single subject (ss) in the absence of an appropriate external reference standard or replicates. To evaluate our proposed all-against-one framework, we construct reference standards (RSs) with five conventional replicate-anchored analyses (NOISeq, DEGseq, edgeR, DESeq, DESeq2) and the remainder were treated separately as single-subject sample pairs for ss analyses (without replicates).ResultsEight ss methods (NOISeq, DEGseq, edgeR, mixture model, DESeq, DESeq2, iDEG, and ensemble) for identifying genes with differential expression were compared in Yeast (parental line versus snf2 deletion mutant; n=42/condition) and a MCF7 breast-cancer cell line (baseline versus stimulated with estradiol; n=7/condition). Receiver-operator characteristic (ROC) and precision-recall plots were determined for eight ss methods against each of the five RSs in both datasets. Consistent with prior analyses of these data, similar to 50% and similar to 15% DEGs were obtained in Yeast and MCF7 datasets respectively, regardless of the RSs method. NOISeq, edgeR, and DESeq were the most concordant for creating a RS. Single-subject versions of NOISeq, DEGseq, and an ensemble learner achieved the best median ROC-area-under-the-curve to compare two transcriptomes without replicates regardless of the RS method and dataset (>90% in Yeast, >0.75 in MCF7). Further, distinct specific single-subject methods perform better according to different proportions of DEGs.ConclusionsThe all-against-one framework provides a honest evaluation framework for single-subject DEG studies since these methods are evaluated, by design, against reference standards produced by unrelated DEG methods. The ss-ensemble method was the only one to reliably produce higher accuracies in all conditions tested in this conservative evaluation framework. However, single-subject methods for identifying DEGs from paired samples need improvement, as no method performed with precision>90% and obtained moderate levels of recall.en_US
dc.description.sponsorshipUniversity of Arizona Health Sciences Center for Biomedical Informatics and Biostatistics; BIO5 Institute; NIH [U01AI122275, HL132532, NCI P30CA023074, 1UG3OD023171, 1S10RR029030]en_US
dc.language.isoenen_US
dc.publisherBMCen_US
dc.rightsCopyright © The Author(s). 2019 Open Access. This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/). The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.en_US
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.subjectGenomic medicineen_US
dc.subjectMedical genomicsen_US
dc.subjectN-of-1en_US
dc.subjectN-of-1 studiesen_US
dc.subjectPrecision medicineen_US
dc.subjectSingle-subject studiesen_US
dc.subjectTranscriptomeen_US
dc.titleEvaluating single-subject study methods for personal transcriptomic interpretations to advance precision medicineen_US
dc.typeArticleen_US
dc.contributor.departmentUniv Arizona Hlth Sci, Ctr Biomed Informat & Biostaten_US
dc.contributor.departmentUniv Arizona, Grad Interdisciplinary Program Staten_US
dc.contributor.departmentUniv Arizona, Dept Math, Coll Scien_US
dc.contributor.departmentUniv Arizona, Ctr Cancen_US
dc.identifier.journalBMC MEDICAL GENOMICSen_US
dc.description.noteOpen access journalen_US
dc.description.collectioninformationThis item from the UA Faculty Publications collection is made available by the University of Arizona with support from the University of Arizona Libraries. If you have questions, please contact us at repository@u.library.arizona.edu.en_US
dc.eprint.versionFinal published versionen_US
dc.source.journaltitleBMC medical genomics
refterms.dateFOA2019-08-22T19:31:12Z


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Copyright © The Author(s). 2019 Open Access. This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/). The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
Except where otherwise noted, this item's license is described as Copyright © The Author(s). 2019 Open Access. This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/). The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.