Mostrar el registro sencillo del ítem
dc.contributor.author | Ugidos, Manuel | es_ES |
dc.contributor.author | Tarazona Campos, Sonia | es_ES |
dc.contributor.author | Prats-Montalbán, José Manuel | es_ES |
dc.contributor.author | Ferrer, Alberto | es_ES |
dc.contributor.author | Conesa, Ana | es_ES |
dc.date.accessioned | 2021-03-05T04:32:24Z | |
dc.date.available | 2021-03-05T04:32:24Z | |
dc.date.issued | 2020-10 | es_ES |
dc.identifier.issn | 0962-2802 | es_ES |
dc.identifier.uri | http://hdl.handle.net/10251/163188 | |
dc.description.abstract | [EN] Diversity of omic technologies has expanded in the last years together with the number of omic data integration strategies. However, multiomic data generation is costly, and many research groups cannot afford research projects where many different omic techniques are generated, at least at the same time. As most researchers share their data in public repositories, different omic datasets of the same biological system obtained at different labs can be combined to construct a multiomic study. However, data obtained at different labs or moments in time are typically subjected to batch effects that need to be removed for successful data integration. While there are methods to correct batch effects on the same data types obtained in different studies, they cannot be applied to correct lab or batch effects across omics. This impairs multiomic meta-analysis. Fortunately, in many cases, at least one omics platform-i.e. gene expression- is repeatedly measured across labs, together with the additional omic modalities that are specific to each study. This creates an opportunity for batch analysis. We have developed MultiBaC (multiomic Multiomics Batch-effect Correction correction), a strategy to correct batch effects from multiomic datasets distributed across different labs or data acquisition events. Our strategy is based on the existence of at least one shared data type which allows data prediction across omics. We validate this approach both on simulated data and on a case where the multiomic design is fully shared by two labs, hence batch effect correction within the same omic modality using traditional methods can be compared with the MultiBaC correction across data types. Finally, we apply MultiBaC to a true multiomic data integration problem to show that we are able to improve the detection of meaningful biological effects. | es_ES |
dc.description.sponsorship | The author(s) disclosed receipt of the following financial support for the research, authorship, and/or publication of this article: This work is part of a research project that is totally funded by Conselleria d'Educacio, Cultura i Esport (Generalitat Valenciana) through PROMETEO grants program for excellence research groups. | es_ES |
dc.language | Inglés | es_ES |
dc.publisher | SAGE Publications | es_ES |
dc.relation.ispartof | Statistical Methods in Medical Research | es_ES |
dc.rights | Reserva de todos los derechos | es_ES |
dc.subject | Batch effect correction | es_ES |
dc.subject | Multiomic integration | es_ES |
dc.subject | Multivariate methods | es_ES |
dc.subject | Biostatistics | es_ES |
dc.subject.classification | ESTADISTICA E INVESTIGACION OPERATIVA | es_ES |
dc.title | MultiBaC: A strategy to remove batch effects between different omic data types | es_ES |
dc.type | Artículo | es_ES |
dc.identifier.doi | 10.1177/0962280220907365 | es_ES |
dc.relation.projectID | info:eu-repo/grantAgreement/GVA//PROMETEO%2F2016%2F093/ES/The Next Systems Biology: desarrollo de métodos estadísticos para la biología de sistemas multiómica/ | es_ES |
dc.rights.accessRights | Abierto | es_ES |
dc.contributor.affiliation | Universitat Politècnica de València. Departamento de Estadística e Investigación Operativa Aplicadas y Calidad - Departament d'Estadística i Investigació Operativa Aplicades i Qualitat | es_ES |
dc.description.bibliographicCitation | Ugidos, M.; Tarazona Campos, S.; Prats-Montalbán, JM.; Ferrer, A.; Conesa, A. (2020). MultiBaC: A strategy to remove batch effects between different omic data types. Statistical Methods in Medical Research. 29(10):2851-2864. https://doi.org/10.1177/0962280220907365 | es_ES |
dc.description.accrualMethod | S | es_ES |
dc.relation.publisherversion | https://doi.org/10.1177/0962280220907365 | es_ES |
dc.description.upvformatpinicio | 2851 | es_ES |
dc.description.upvformatpfin | 2864 | es_ES |
dc.type.version | info:eu-repo/semantics/publishedVersion | es_ES |
dc.description.volume | 29 | es_ES |
dc.description.issue | 10 | es_ES |
dc.identifier.pmid | 32131696 | es_ES |
dc.relation.pasarela | S\408088 | es_ES |
dc.contributor.funder | Generalitat Valenciana | es_ES |
dc.description.references | Kupfer, P., Guthke, R., Pohlers, D., Huber, R., Koczan, D., & Kinne, R. W. (2012). Batch correction of microarray data substantially improves the identification of genes differentially expressed in Rheumatoid Arthritis and Osteoarthritis. BMC Medical Genomics, 5(1). doi:10.1186/1755-8794-5-23 | es_ES |
dc.description.references | Gregori, J., Villarreal, L., Méndez, O., Sánchez, A., Baselga, J., & Villanueva, J. (2012). Batch effects correction improves the sensitivity of significance tests in spectral counting-based comparative discovery proteomics. Journal of Proteomics, 75(13), 3938-3951. doi:10.1016/j.jprot.2012.05.005 | es_ES |
dc.description.references | Ritchie, M. E., Phipson, B., Wu, D., Hu, Y., Law, C. W., Shi, W., & Smyth, G. K. (2015). limma powers differential expression analyses for RNA-sequencing and microarray studies. Nucleic Acids Research, 43(7), e47-e47. doi:10.1093/nar/gkv007 | es_ES |
dc.description.references | Gagnon-Bartsch, J. A., & Speed, T. P. (2011). Using control genes to correct for unwanted variation in microarray data. Biostatistics, 13(3), 539-552. doi:10.1093/biostatistics/kxr034 | es_ES |
dc.description.references | Nueda, M. j., Ferrer, A., & Conesa, A. (2011). ARSyN: a method for the identification and removal of systematic noise in multifactorial time course microarray experiments. Biostatistics, 13(3), 553-566. doi:10.1093/biostatistics/kxr042 | es_ES |
dc.description.references | Jansen, J. J., Hoefsloot, H. C. J., van der Greef, J., Timmerman, M. E., Westerhuis, J. A., & Smilde, A. K. (2005). ASCA: analysis of multivariate data obtained from an experimental design. Journal of Chemometrics, 19(9), 469-481. doi:10.1002/cem.952 | es_ES |
dc.description.references | Nueda, M. J., Conesa, A., Westerhuis, J. A., Hoefsloot, H. C. J., Smilde, A. K., Talón, M., & Ferrer, A. (2007). Discovering gene expression patterns in time course microarray experiments by ANOVA–SCA. Bioinformatics, 23(14), 1792-1800. doi:10.1093/bioinformatics/btm251 | es_ES |
dc.description.references | Giordan, M. (2013). A Two-Stage Procedure for the Removal of Batch Effects in Microarray Studies. Statistics in Biosciences, 6(1), 73-84. doi:10.1007/s12561-013-9081-1 | es_ES |
dc.description.references | Nyamundanda, G., Poudel, P., Patil, Y., & Sadanandam, A. (2017). A Novel Statistical Method to Diagnose, Quantify and Correct Batch Effects in Genomic Studies. Scientific Reports, 7(1). doi:10.1038/s41598-017-11110-6 | es_ES |
dc.description.references | Reese, S. E., Archer, K. J., Therneau, T. M., Atkinson, E. J., Vachon, C. M., de Andrade, M., … Eckel-Passow, J. E. (2013). A new statistic for identifying batch effects in high-throughput genomic data that uses guided principal component analysis. Bioinformatics, 29(22), 2877-2883. doi:10.1093/bioinformatics/btt480 | es_ES |
dc.description.references | Papiez, A., Marczyk, M., Polanska, J., & Polanski, A. (2018). BatchI: Batch effect Identification in high-throughput screening data using a dynamic programming algorithm. Bioinformatics, 35(11), 1885-1892. doi:10.1093/bioinformatics/bty900 | es_ES |
dc.description.references | Keel, B. N., Zarek, C. M., Keele, J. W., Kuehn, L. A., Snelling, W. M., Oliver, W. T., … Lindholm-Perry, A. K. (2018). RNA-Seq Meta-analysis identifies genes in skeletal muscle associated with gain and intake across a multi-season study of crossbred beef steers. BMC Genomics, 19(1). doi:10.1186/s12864-018-4769-8 | es_ES |
dc.description.references | Li, M. D., Burns, T. C., Morgan, A. A., & Khatri, P. (2014). Integrated multi-cohort transcriptional meta-analysis of neurodegenerative diseases. Acta Neuropathologica Communications, 2(1). doi:10.1186/s40478-014-0093-y | es_ES |
dc.description.references | Andres-Terre, M., McGuire, H. M., Pouliot, Y., Bongen, E., Sweeney, T. E., Tato, C. M., & Khatri, P. (2015). Integrated, Multi-cohort Analysis Identifies Conserved Transcriptional Signatures across Multiple Respiratory Viruses. Immunity, 43(6), 1199-1211. doi:10.1016/j.immuni.2015.11.003 | es_ES |
dc.description.references | Sandhu, V., Labori, K. J., Borgida, A., Lungu, I., Bartlett, J., Hafezi-Bakhtiari, S., … Haibe-Kains, B. (2019). Meta-Analysis of 1,200 Transcriptomic Profiles Identifies a Prognostic Model for Pancreatic Ductal Adenocarcinoma. JCO Clinical Cancer Informatics, (3), 1-16. doi:10.1200/cci.18.00102 | es_ES |
dc.description.references | Huang, H., Liu, C.-C., & Zhou, X. J. (2010). Bayesian approach to transforming public gene expression repositories into disease diagnosis databases. Proceedings of the National Academy of Sciences, 107(15), 6823-6828. doi:10.1073/pnas.0912043107 | es_ES |
dc.description.references | Pelechano, V., & Pérez-Ortín, J. E. (2010). There is a steady-state transcriptome in exponentially growing yeast cells. Yeast, 27(7), 413-422. doi:10.1002/yea.1768 | es_ES |
dc.description.references | Garcı́a-Martı́nez, J., Aranda, A., & Pérez-Ortı́n, J. E. (2004). Genomic Run-On Evaluates Transcription Rates for All Yeast Genes and Identifies Gene Regulatory Mechanisms. Molecular Cell, 15(2), 303-313. doi:10.1016/j.molcel.2004.06.004 | es_ES |
dc.description.references | Pelechano, V., Chávez, S., & Pérez-Ortín, J. E. (2010). A Complete Set of Nascent Transcription Rates for Yeast Genes. PLoS ONE, 5(11), e15442. doi:10.1371/journal.pone.0015442 | es_ES |
dc.description.references | Zid, B. M., & O’Shea, E. K. (2014). Promoter sequences direct cytoplasmic localization and translation of mRNAs during starvation in yeast. Nature, 514(7520), 117-121. doi:10.1038/nature13578 | es_ES |
dc.description.references | Freeberg, M. A., Han, T., Moresco, J. J., Kong, A., Yang, Y.-C., Lu, Z., … Kim, J. K. (2013). Pervasive and dynamic protein binding sites of the mRNA transcriptome in Saccharomyces cerevisiae. Genome Biology, 14(2), R13. doi:10.1186/gb-2013-14-2-r13 | es_ES |
dc.description.references | McKinlay, A., Araya, C. L., & Fields, S. (2011). Genome-Wide Analysis of Nascent Transcription in Saccharomyces cerevisiae. G3 Genes|Genomes|Genetics, 1(7), 549-558. doi:10.1534/g3.111.000810 | es_ES |
dc.description.references | Castells-Roca, L., García-Martínez, J., Moreno, J., Herrero, E., Bellí, G., & Pérez-Ortín, J. E. (2011). Heat Shock Response in Yeast Involves Changes in Both Transcription Rates and mRNA Stabilities. PLoS ONE, 6(2), e17272. doi:10.1371/journal.pone.0017272 | es_ES |
dc.description.references | Wold, S., Sjöström, M., & Eriksson, L. (2001). PLS-regression: a basic tool of chemometrics. Chemometrics and Intelligent Laboratory Systems, 58(2), 109-130. doi:10.1016/s0169-7439(01)00155-1 | es_ES |
dc.description.references | Folch-Fortuny, A., Vitale, R., de Noord, O. E., & Ferrer, A. (2017). Calibration transfer between NIR spectrometers: New proposals and a comparative study. Journal of Chemometrics, 31(3), e2874. doi:10.1002/cem.2874 | es_ES |
dc.description.references | García Muñoz, S., MacGregor, J. F., & Kourti, T. (2005). Product transfer between sites using Joint-Y PLS. Chemometrics and Intelligent Laboratory Systems, 79(1-2), 101-114. doi:10.1016/j.chemolab.2005.04.009 | es_ES |
dc.description.references | Andrade, J. M., Gómez-Carracedo, M. P., Krzanowski, W., & Kubista, M. (2004). Procrustes rotation in analytical chemistry, a tutorial. Chemometrics and Intelligent Laboratory Systems, 72(2), 123-132. doi:10.1016/j.chemolab.2004.01.007 | es_ES |
dc.description.references | Hurley, J. R., & Cattell, R. B. (2007). The procrustes program: Producing direct rotation to test a hypothesized factor structure. Behavioral Science, 7(2), 258-262. doi:10.1002/bs.3830070216 | es_ES |
dc.description.references | Hartigan, J. A., & Wong, M. A. (1979). Algorithm AS 136: A K-Means Clustering Algorithm. Applied Statistics, 28(1), 100. doi:10.2307/2346830 | es_ES |