Critical review of reporting of the data analysis step in metabolomics

被引:51
|
作者
Considine, E. C. [1 ]
Thomas, G. [2 ]
Boulesteix, A. L. [3 ]
Khashan, A. S. [1 ,4 ]
Kenny, L. C. [1 ]
机构
[1] Univ Coll Cork, Dept Obstet & Gynaecol, Irish Ctr Fetal & Neonatal Translat Res INFANT, Cork, Ireland
[2] SQU4RE, Sint Alfonsusstr 17, B-8800 Roeselare, Belgium
[3] Ludwig Maximilians Univ Munchen, Dept Med Informat Biometry & Epidemiol, Marchioninistr 15, D-81377 Munich, Germany
[4] Univ Coll Cork, Dept Epidemiol & Publ Hlth, Cork, Ireland
基金
爱尔兰科学基金会;
关键词
Data analysis; Reporting; Minimum standards; Biomarker discovery; Metabolomics; Guidelines; STATISTICAL-ANALYSIS; MINIMUM INFORMATION; BIOLOGICAL SAMPLES; EARLY-DIAGNOSIS; SERUM; BIOMARKERS; STANDARDS; CANCER; NMR; REQUIREMENTS;
D O I
10.1007/s11306-017-1299-3
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Introduction We present the first study to critically appraise the quality of reporting of the data analysis step in metabolomics studies since the publication of minimum reporting guidelines in 2007. Objectives The aim of this study was to assess the standard of reporting of the data analysis step in metabolomics biomarker discovery studies and to investigate whether the level of detail supplied allows basic understanding of the steps employed and/or reuse of the protocol. For the purposes of this review we define the data analysis step to include the data pretreatment step and the actual data analysis step, which covers algorithm selection, univariate analysis and multivariate analysis. Method We reviewed the literature to identify metabolomic studies of biomarker discovery that were published between January 2008 and December 2014. Studies were examined for completeness in reporting the various steps of the data pretreatment phase and data analysis phase and also for clarity of the workflow of these sections. Results We analysed 27 papers, published anytime in 2008 until the end of 2014 in the area or biomarker discovery in serum metabolomics. The results of this review showed that the data analysis step in metabolomics biomarker discovery studies is plagued by unclear and incomplete reporting. Major omissions and lack of logical flow render the data analysis' workflows in these studies impossible to follow and therefore replicate or even imitate. Conclusions While we await the holy grail of computational reproducibility in data analysis to become standard, we propose that, at a minimum, the data analysis section of metabolomics studies should be readable and interpretable without omissions such that a data analysis workflow diagram could be extrapolated from the study and therefore the data analysis protocol could be reused by the reader. That inconsistent and patchy reporting obfuscates reproducibility is a given. However even basic understanding and reuses of protocols are hampered by the low level of detail supplied in the data analysis sections of the studies that we reviewed.
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收藏
页数:16
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