Literature DB >> 32087354

Towards the development of an omics data analysis framework.

Marcha Verheijen1, Weida Tong2, Leming Shi3, Timothy W Gant4, Bruce Seligman5, Florian Caiment6.   

Abstract

The use of various omics techniques for scientific research is increasing. While toxicogenomics studies have already produced substantial data on diverse omics platforms, to date there has been little routine application in regulatory toxicology. This is despite the promises and excitement of 20 years ago when it was widely speculated that omics methods would reduce or even replace animal use and allow a much enhanced understanding of hazard and susceptibility. One of the reasons for this has been a trepidation about relying on the produced data. It has been argued that omics outputs might not be sufficiently reliable for regulatory application because the techniques, bioinformatics and interpretation can vary. For these reasons the robustness of the obtained results is questioned. This reticence to trust omics data is further magnified by the lack of internationally agreed upon guidelines and protocols for both the generation and processing of omics data. One way forward would be to reach a consensus on an omics data analysis framework (ODAF) for regulatory application (R-ODAF) based on rigorous data analysis. The authors of this article are involved in a Long-Range Research Initiative (LRI) project that will propose an R-ODAF for transcriptomics data. The R-ODAF will then be reviewed and evaluated by the main regulatory agencies and consensus forums such as the Organization for Economic Co-operation and Development (OECD). This work builds on The MicroArray Quality Control work that developed standards for the generation of data from microarrays and sequencing but not for reporting or analysis.
Copyright © 2020. Published by Elsevier Inc.

Keywords:  Data-analysis framework; Regulatory agencies; Toxicogenomics; Toxicology; Transcriptomics

Mesh:

Year:  2020        PMID: 32087354     DOI: 10.1016/j.yrtph.2020.104621

Source DB:  PubMed          Journal:  Regul Toxicol Pharmacol        ISSN: 0273-2300            Impact factor:   3.271


  2 in total

1.  Progress towards an OECD reporting framework for transcriptomics and metabolomics in regulatory toxicology.

Authors:  Joshua A Harrill; Mark R Viant; Carole L Yauk; Magdalini Sachana; Timothy W Gant; Scott S Auerbach; Richard D Beger; Mounir Bouhifd; Jason O'Brien; Lyle Burgoon; Florian Caiment; Donatella Carpi; Tao Chen; Brian N Chorley; John Colbourne; Raffaella Corvi; Laurent Debrauwer; Claire O'Donovan; Timothy M D Ebbels; Drew R Ekman; Frank Faulhammer; Laura Gribaldo; Gina M Hilton; Stephanie P Jones; Aniko Kende; Thomas N Lawson; Sofia B Leite; Pim E G Leonards; Mirjam Luijten; Alberto Martin; Laura Moussa; Serge Rudaz; Oliver Schmitz; Tomasz Sobanski; Volker Strauss; Monica Vaccari; Vikrant Vijay; Ralf J M Weber; Antony J Williams; Andrew Williams; Russell S Thomas; Maurice Whelan
Journal:  Regul Toxicol Pharmacol       Date:  2021-07-29       Impact factor: 3.598

Review 2.  Translational precision medicine: an industry perspective.

Authors:  Dominik Hartl; Valeria de Luca; Anna Kostikova; Jason Laramie; Scott Kennedy; Enrico Ferrero; Richard Siegel; Martin Fink; Sohail Ahmed; John Millholland; Alexander Schuhmacher; Markus Hinder; Luca Piali; Adrian Roth
Journal:  J Transl Med       Date:  2021-06-05       Impact factor: 5.531

  2 in total

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