No retraction, correction or concern found when last checked on Oct 16, 2026.
Guidelines for Developing and Reporting Machine Learning Predictive Models in Biomedical Research: A Multidisciplinary View
Wei Luo, Dinh Phung, Truyen Tran and 9 more
Journal of Medical Internet Research · 2016
Abstract
Background. As more and more researchers are turning to big data for new opportunities of biomedical discoveries, machine learning models, as the backbone of big data analysis, are mentioned more often in biomedical journals. However, owing to the inherent complexity of machine learning methods, they are prone to misuse. Because of the flexibility in specifying machine learning models, the results are often insufficiently reported in research articles, hindering reliable assessment of model validity and consistent interpretation of model outputs.
Objective. To attain a set of guidelines on the use of machine learning predictive models within clinical settings to make sure the models are correctly applied and sufficiently reported so that true discoveries can be distinguished from random coincidence.
Methods. A multidisciplinary panel of machine learning experts, clinicians, and traditional statisticians were interviewed, using an iterative process in accordance with the Delphi method.
Results. The process produced a set of guidelines that consists of (1) a list of reporting items to be included in a research article and (2) a set of practical sequential steps for developing predictive models.
Conclusions. A set of guidelines was generated to enable correct application of machine learning models and consistent reporting of model specifications and results in biomedical research. We believe that such guidelines will accelerate the adoption of big data analysis, particularly with machine learning methods, in the biomedical research community.
Full text
From PubMed Central, U.S. National Library of Medicine, as current on Oct 16, 2026. Paragraph numbers are ours, so an answer can point at one.
Introduction
Big data is changing every industry. Medicine is no exception. With rapidly growing volume and diversity of data in health care and biomedical research, traditional statistical methods often are inadequate. By looking into other industries where modern machine learning techniques play central roles in dealing with big data, many health and biomedical researchers have started applying machine learning to extract valuable insights from ever-growing biomedical databases, in particular with predictive models. The flexibility and prowess of machine learning models also enable us to leverage novel but extremely valuable sources of information, such as wearable device data and electronic health record data.
Despite its popularity, it is difficult to find a universally agreed-upon definition for machine learning. Arguably, many machine learning methods can be traced back as far as 30 years ago. However, machine learning started making a broad impact only in the last 10 years. The reviews by Jordan and Mitchell and Ghahramani provide accessible overviews for machine learning. In this paper, we focus on machine learning predictive methods and models. These include random forest, support vector machines, and other methods listed in Multimedia Appendix 1. They all share an important difference from the traditional statistical methods such as logistic regression or analysis of variance—the ability to make accurate predictions on unseen data. To optimize the prediction accuracy, often the methods do not attempt to produce interpretable models. This also allows them to handle a large number of variables common in most big data problems.
Accompanying the flexibility of emerging machine learning techniques, however, is uncertainty and inconsistency in the use of such techniques. Machine learning, owing to its intrinsic mathematical and algorithmic complexity, is often considered a “black magic” that requires a delicate balance of a large number of conflicting factors. This, together with inadequate reporting of data sources and modeling process, makes research results reported in many biomedical papers difficult to interpret. It is not rare to see potentially spurious conclusions drawn from methodologically inadequate studies, which in turn compromises the credibility of other valid studies and discourages many researchers who could benefit from adopting machine learning techniques.
Most pitfalls of applying machine learning techniques in biomedical research originate from a small number of common issues, including data leakage and overfitting, which can be avoided by adopting a set of best practice standards. Recognizing the urgent need for such a standard, we created a minimum list of reporting items and a set of guidelines for optimal use of predictive models in biomedical research.
Panel of Experts
In 2015, a multidisciplinary panel was assembled to cover expertise in machine learning, traditional statistics, and biomedical applications of these methods. The candidate list was generated in two stages. The panel grew from a number of active machine learning researchers attending international conferences including the Asian Conference on Machine Learning, the Pacific Asia Conference on Knowledge Discovery and Data Mining, and the International Conference on Pattern Recognition. The responders were then asked to nominate additional researchers who apply machine learning in biomedical research. Effort was exercised to include researchers from different continents. Researchers from the list were approached through emails for joining the panel and/or recommending colleagues to be included. Two declined the invitation.
The final panel included 11 researchers from 3 institutions on 3 different continents. Each panelist had experience and expertise in machine learning projects in biomedical applications and has learned from common pitfalls. The areas of research expertise included machine learning, data mining, computational intelligence, signal processing, information management, bioinformatics, and psychiatry. On average, each panel member had 8.5 years’ experience in either developing or applying machine learning methods. The diversity of the panel was reflected by the members’ affiliation with 3 different institutions across 3 continents.
Development of Guidelines
Using an iterative process, the panel produced a set of guidelines that consists of (1) a list of reporting items to be included in a research article and (2) a set of practical sequential steps for developing predictive models. The Delphi method was used to generate the list of reporting items.
The panelists were interviewed with multiple iterations of emails. Email 1 asked panelists to list topics to be covered in the guidelines. An aggregated topic list was generated. Email 2 asked each panelist to review the scope of the list and state his or her recommendation for each topic in the aggregated list. Later iterations of email interviews were organized to evolve the list until all experts agreed on the list. Because of the logistic complexity of coordinating the large panel, we took a grow-shrink approach. In the growing phase, all suggested items were included, even an item suggested by only 1 panelist. In the shrinking phase, any item opposed by a panelist was excluded. As it turned out, most items were initially suggested by a panelist but seconded by other panelists, suggesting the importance of the group effort for covering most important topics.
The practical steps were developed by machine learning experts in their respective areas and finally approved by the panel. During the process, the panelists consulted extensively the broad literature on machine learning and predictive model in particular.
Results
A total of 4 iterations of emails resulted in the final form of the guidelines. Email 1 generated diverse responses in terms of topics. However the final scope was generally agreed upon. For email 2, most panelists commented on only a subset of topics (mostly the ones suggested by themselves). No recommendations generated significant disagreement except for minor wording decisions and quantifying conditions.
The final results included a list of reporting items (Tables 1-5,Textboxes 1-4, and Figure 1) and a template flowchart for reporting data used for training and testing predictive models, including both internal validation and external validation (Figure 2).
Recognizing the broad meaning of the term “machine learning,” we distinguish essential items from desirable items (using appropriate footnotes in the tables). The essential items should be included in any report, unless there is a strong reason indicating otherwise; the desirable items should be reported whenever applicable.
Leakage refers to the unintended use of known information as unknown. There are two kinds of leakage: outcome leakage and validation leakage. In outcome leakage, independent variables incorporate elements that can be used to easily infer outcomes. For example, a risk factor that spans into the future may be used to predict the future itself. In the validation leakage, ground truth from the training set may propagate to the validation set. For example, when the same patient is used in both training and validation, the future outcome in the training may overlap with the future outcome in the validation. In both leakage cases, the performance obtained is overoptimistic.
Calibration of a prediction model refers to the agreement between the predictions made by the model and the observed outcomes. As an example, if the prediction model predicts 70% risk of mortality in the next 1 year for a patient with lung cancer, then the model is well calibrated if in our dataset approximately 70% of patients with lung cancer die within the next 1 year.
Often, the regularized prediction may create bias in a model. Therefore, it is advisable to check for the calibration. In the case of regression models, the calibration can be easily assessed graphically by marking prediction scores on the x-axis and the true outcomes on the y-axis. In the case of binary classification, the y-axis has only 0 and 1 values; however, smoothing techniques such as LOESS algorithm may be used to estimate the observed probabilities for the outcomes. In a more systematic way, one can perform the Hosmer-Lemeshow test to measure the goodness of fit of the model. The test assesses whether the observed event rates match the predicted event rates in subgroups of the model population.
When a categorical predictor variable can take an uncommon value, there may be only a small number of observations having that value. In a classification problem, these few observations by chance may have the same response value. Such “perfect” predictors may cause overfitting, especially when tree-based models are used. Therefore, special treatment is required.
One conservative approach is to remove all dummy variables corresponding to rare categories. We recommend a cutoff of 10 observations.
For modeling methods with feature selection built in, an alternative approach is to first fit a model with all independent variables. If the resulting model is only marginally influenced by the rare categories, then the model can be kept. Otherwise, the rare categories showing high “importance” score are removed and the model refitted.
K-fold validation refers to the practice of splitting the derivation data into K equal parts. The model is then trained on K−1 parts and validated on the remaining part. The process is repeated K times. The average results for K-folds are then reported. For small classes and rare categorical factors, stratified K-fold splitting should be used to ensure the equal presence of these classes and factors in each fold.
Discussion
We have generated a set of guidelines that will enable correct application of machine learning models and consistent reporting of model specifications and results in biomedical research.
Because of the broad range of machine learning methods that can be used in biomedical applications, we involved a large number of stakeholders, as either developers of machine learning methods or users of these methods in biomedicine research.
The guidelines here cover most popular machine learning methods appearing in biomedical studies. We believe that such guidelines will accelerate the adoption of big data analysis, particularly with machine learning methods, in the biomedical research community.
Although the proposed guidelines result from a voluntary effort without dedicated funding support, we still managed to assemble a panel of researchers from multiple disciplines, multiple institutions, and multiple continents. We hope the guidelines can result in more people contributing their knowledge and experience in the discussion.
As machine learning is a rapidly developing research area, the guidelines are not expected to cover every aspect of the modeling process. The guidelines are expected to evolve as research in biomedicine and machine learning progresses.
References 55
- 1.
Ayaru L, Ypsilantis P, Nanapragasam A, Choi RC, Thillanathan A, Min-Ho L, Montana G. Prediction of outcome in acute lower gastrointestinal bleeding using gradient boosting. PLoS One. 2015;10(7):e0132485.
Not in our library10.1371/journal.pone.0132485
- 2.
- 3.
Tran T, Luo W, Phung D, Harvey R, Berk M, Kennedy RL, Venkatesh S. Risk stratification using data from electronic medical records better predicts suicide risks than clinician assessments. BMC Psychiatry. 2014;14:76.
Not in our library10.1186/1471-244x-14-76
- 4.
Breiman L, Friedman J, Stone C, Olshen R. Classification and regression trees. 1984.
Not in our library
- 5.
Jordan MI, Mitchell TM. Machine learning: trends, perspectives, and prospects. Science. 2015;349(6245):255-60.
Not in our library10.1126/science.aaa8415
- 6.
Ghahramani Z. Probabilistic machine learning and artificial intelligence. Nature. 2015;521(7553):452-9.
Not in our library10.1038/nature14541
- 7.
Bone D, Goodwin MS, Black MP, Lee C, Audhkhasi K, Narayanan S. Applying machine learning to facilitate autism diagnostics: pitfalls and promises. J Autism Dev Disord. 2015;45(5):1121-36.
Not in our library10.1007/s10803-014-2268-6
- 8.
Metaxas P, Mustafaraj E, Gayo-Avello D. How (not) to predict elections. 2011.
Not in our library
- 9.
Jungherr A, Jurgens P, Schoen H. Why the pirate party won the German election of 2009 or the trouble with predictions: a response to Tumasjan A, Sprenger TO, Sander PG, & Welpe IM “Predicting elections with Twitter: what 140 characters reveal about political sentiment”. Social Science Computer Review. 2011;30(2):229-234.
Not in our library10.1177/0894439311404119
- 10.
Lazer D, Kennedy R, King G, Vespignani A. Big data. The parable of Google flu: traps in big data analysis. Science. 2014;343(6176):1203-5.
Not in our library10.1126/science.1248506
- 11.
- 12.
Smialowski P, Frishman D, Kramer S. Pitfalls of supervised feature selection. Bioinformatics. 2010;26(3):440-3.
Not in our library10.1093/bioinformatics/btp621
- 13.
Babyak M. What you see may not be what you get: a brief, nontechnical introduction to overfitting in regression-type models. Psychosom Med. 2004;66(3):411-21.
Not in our library10.1097/01.psy.0000127692.23278.a9
- 14.
Hawkins DM. The problem of overfitting. J Chem Inf Comput Sci. 2004;44(1):1-12.
Not in our library10.1021/ci0342472
- 15.
Subramanian J, Simon R. Overfitting in prediction models - is it a problem only in high dimensions? Contemp Clin Trials. 2013;36(2):636-41.
Not in our library10.1016/j.cct.2013.06.011
- 16.
Hastie T, Tibshirani R, Friedman J. The elements of statistical learning: data mining, inference and prediction. 2009.
Not in our library
- 17.
Kuhn M, Johnson K. Applied predictive modeling. 2013.
Not in our library
- 18.
Steyerberg E. Clinical Prediction Models: A Practical Approach to Development, Validation, and Updating (Statistics for Biology and Health). 2009.
Not in our library
- 19.
Cox D. Two further applications of a model for binary regression. Biometrika. 1958;45(3/4):562-565.
Not in our library10.2307/2333203
- 20.
Quinlan J. Simplifying decision trees. Int J Man Mach Stud. 1987;27(3):221-234.
Not in our library10.1016/s0020-7373(87)80053-6
- 21.
Quinlan J. Induction of decision trees. Mach Learn. 1986;1(1):81-106.
Not in our library10.1007/bf00116251
- 22.
Podgorelec V, Kokol P, Stiglic B, Rozman I. Decision trees: an overview and their use in medicine. J Med Syst. 2002;26(5):445-63.
Not in our library10.1023/a:1016409317640
- 23.
Kotsiantis S. Decision trees: a recent overview. Artif Intell Rev. 2011;39(4):261-283.
Not in our library10.1007/s10462-011-9272-4
- 24.
Kingsford C, Salzberg SL. What are decision trees? Nat Biotechnol. 2008;26(9):1011-3.
Not in our library10.1038/nbt0908-1011
- 25.
Luo W, Gallagher M. Unsupervised DRG upcoding detection in healthcare databases. 2010;600-605.
Not in our library10.1109/icdmw.2010.108
- 26.
Siddique J, Ruhnke GW, Flores A, Prochaska MT, Paesch E, Meltzer DO, Whelan CT. Applying classification trees to hospital administrative data to identify patients with lower gastrointestinal bleeding. PLoS One. 2015;10(9):e0138987.
Not in our library10.1371/journal.pone.0138987
- 27.
Bae S, Lee SA, Lee SH. Prediction by data mining, of suicide attempts in Korean adolescents: a national study. Neuropsychiatr Dis Treat. 2015;11:2367-75.
Not in our library10.2147/ndt.s91111
- 28.
Satomi J, Ghaibeh AA, Moriguchi H, Nagahiro s. Predictability of the future development of aggressive behavior of cranial dural arteriovenous fistulas based on decision tree analysis. J Neurosurg. 2015;123(1):86-90.
Not in our library10.3171/2014.10.jns141429
- 29.
Breiman L. Random forests. Mach Learn. 2001;45(1):5-32.
Not in our library10.1023/a:1010933404324
- 30.
Boulesteix A, Janitza S, Kruppa J, König Ir. Overview of random forest methodology and practical guidance with emphasis on computational biology and bioinformatics. WIREs Data Mining Knowl Discov. 2012;2(6):493-507.
Not in our library10.1002/widm.1072
- 31.
Strobl C, Malley J, Tutz G. An introduction to recursive partitioning: rationale, application, and characteristics of classification and regression trees, bagging, and random forests. Psychol Methods. 2009;14(4):323-48.
Not in our library10.1037/a0016973
- 32.
Touw W, Bayjanov JR, Overmars L, Backus L, Boekhorst J, Wels M, van Hijum SA. Data mining in the Life Sciences with random forest: a walk in the park or lost in the jungle? Brief Bioinform. 2013;14(3):315-26.
Not in our library10.1093/bib/bbs034
- 33.
Asaoka R, Iwase A, Tsutsumi T, Saito H, Otani S, Miyata K, Murata H, Mayama C, Araie M. Combining multiple HRT parameters using the 'Random Forests' method improves the diagnostic accuracy of glaucoma in emmetropic and highly myopic eyes. Invest Ophthalmol Vis Sci. 2014;55(4):2482-90.
Not in our library10.1167/iovs.14-14009
- 34.
Yoshida T, Iwase A, Hirasawa H, Murata H, Mayama C, Araie M, Asaoka R. Discriminating between glaucoma and normal eyes using optical coherence tomography and the 'Random Forests' classifier. PLoS One. 2014;9(8):e106117.
Not in our library10.1371/journal.pone.0106117
- 35.
Tibshirani R. Regression shrinkage and selection via the lasso. J R Stat Soc Series B Stat Methodol. 1996;267-288.
Not in our library
- 36.
Tibshirani R. Regression shrinkage and selection via the lasso: a retrospective. Journal of the Royal Statistical Societyries B (Statistical Methodology). 2011;73(3):273-282.
Not in our library10.1111/j.1467-9868.2011.00771.x
- 37.
Vidaurre D, Bielza C, Larrañaga P. A survey of L1 regression. Int Stat Rev. 2013;81(3):361-387.
Not in our library10.1111/insr.12023
- 38.
Hesterberg T, Choi Nh, Meier L, Fraley C. Least angle and ℓ 1 penalized regression: A review. Statist Surv. 2008;2:61-93.
Not in our library10.1214/08-ss035
- 39.
Fujino Y, Murata H, Mayama C, Asaoka R. Applying “lasso” regression to predict future visual field progression in glaucoma patients. Invest Ophthalmol Vis Sci. 2015;56(4):2334-9.
Not in our library10.1167/iovs.15-16445
- 40.
Shimizu Y, Yoshimoto J, Toki S, Takamura M, Yoshimura S, Okamoto Y, Yamawaki S, Doya K. Toward probabilistic diagnosis and understanding of depression based on functional MRI data analysis with logistic group LASSO. PLoS One. 2015;10(5):e0123524.
Not in our library10.1371/journal.pone.0123524
Cited by papers we hold 14
- Machine learning algorithms for prediction of cerebrospinal fluid leakage after posterior surgery for thoracic ossification of the ligamentum flavum · 2025Not checked
- METhodological RadiomICs Score (METRICS): a quality scoring tool for radiomics research endorsed by EuSoMII · 2024No notice
- Reporting guidelines in medical artificial intelligence: a systematic review and meta-analysis · 2024No notice
- A machine learning approach to predict e-cigarette use and dependence among Ontario youth · 2022Not checked
- Guidelines and quality criteria for artificial intelligence-based prediction models in healthcare: a scoping review · 2022No notice
- Digital health tools for the passive monitoring of depression: a systematic review of methods · 2022No notice
- Artificial Intelligence Predicts Cost After Ambulatory Anterior Cruciate Ligament Reconstruction · 2021Not checked
- A Risk Prediction Model Based on Machine Learning for Cognitive Impairment Among Chinese Community-Dwelling Elderly People With Normal Cognition: Development and Validation Study · 2021No notice
- Letter to the editor: Response to Giardiello D, Antoniou AC, Mariani L, Easton DF, Steyerberg EW · 2020Not checked
- Early detection of type 2 diabetes mellitus using machine learning-based prediction models · 2020No notice
- Machine Learning–Guided Adjuvant Treatment of Head and Neck Cancer · 2020No notice
- Methods in predictive techniques for mental health status on social media: a critical review · 2020No notice
- Applications of Machine Learning in Real-Life Digital Health Interventions: Review of the Literature · 2019No notice
- Continuous Monitoring of Vital Signs Using Wearable Devices on the General Ward: Pilot Study · 2017No notice
Reads
Read by people on this page
None yet.
Checked or read by AI through naulon
None yet.
A person counts once a day per paper. We keep no cookie and no address: a reader is a hash that changes every day. Any month under five reads shows no number.
Are you an author?
Is this your paper?
Claim it to add your note and be paid when agents cite it. Free.