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Evaluating single-subject study methods for personal transcriptomic interpretations to advance precision medicine

BACKGROUND: 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 thera...

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Autores principales: Rachid Zaim, Samir, Kenost, Colleen, Berghout, Joanne, Vitali, Francesca, Zhang, Helen Hao, Lussier, Yves A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6624180/
https://www.ncbi.nlm.nih.gov/pubmed/31296218
http://dx.doi.org/10.1186/s12920-019-0513-8
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author Rachid Zaim, Samir
Kenost, Colleen
Berghout, Joanne
Vitali, Francesca
Zhang, Helen Hao
Lussier, Yves A.
author_facet Rachid Zaim, Samir
Kenost, Colleen
Berghout, Joanne
Vitali, Francesca
Zhang, Helen Hao
Lussier, Yves A.
author_sort Rachid Zaim, Samir
collection PubMed
description BACKGROUND: 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). RESULTS: Eight 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, ~ 50% and ~ 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. CONCLUSIONS: The “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. http://www.lussiergroup.org/publications/EnsembleBiomarker
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spelling pubmed-66241802019-07-23 Evaluating single-subject study methods for personal transcriptomic interpretations to advance precision medicine Rachid Zaim, Samir Kenost, Colleen Berghout, Joanne Vitali, Francesca Zhang, Helen Hao Lussier, Yves A. BMC Med Genomics Research BACKGROUND: 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). RESULTS: Eight 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, ~ 50% and ~ 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. CONCLUSIONS: The “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. http://www.lussiergroup.org/publications/EnsembleBiomarker BioMed Central 2019-07-11 /pmc/articles/PMC6624180/ /pubmed/31296218 http://dx.doi.org/10.1186/s12920-019-0513-8 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. 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.
spellingShingle Research
Rachid Zaim, Samir
Kenost, Colleen
Berghout, Joanne
Vitali, Francesca
Zhang, Helen Hao
Lussier, Yves A.
Evaluating single-subject study methods for personal transcriptomic interpretations to advance precision medicine
title Evaluating single-subject study methods for personal transcriptomic interpretations to advance precision medicine
title_full Evaluating single-subject study methods for personal transcriptomic interpretations to advance precision medicine
title_fullStr Evaluating single-subject study methods for personal transcriptomic interpretations to advance precision medicine
title_full_unstemmed Evaluating single-subject study methods for personal transcriptomic interpretations to advance precision medicine
title_short Evaluating single-subject study methods for personal transcriptomic interpretations to advance precision medicine
title_sort evaluating single-subject study methods for personal transcriptomic interpretations to advance precision medicine
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6624180/
https://www.ncbi.nlm.nih.gov/pubmed/31296218
http://dx.doi.org/10.1186/s12920-019-0513-8
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