ArticleBioinformatics (Oxford, England)2014
Robust clinical outcome prediction based on Bayesian analysis of transcriptional profiles and prior causal networks.
Article in Bioinformatics (Oxford, England), 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
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Who cites it
14 citing papers in PubMed, 26 citations in OpenAlex.
- Using machine learning to predict clinical remission with exclusive enteral nutrition in pediatric Crohn disease.Journal of pediatric gastroenterology and nutrition · 2026Article
- Pathogenesis and precision medicine for predicting response in inflammatory bowel disease: advances and future directions.eGastroenterology · 2024Review
- Artificial Intelligence in Inflammatory Bowel Disease Endoscopy: Implications for Clinical Trials.Journal of Crohn's & colitis · 2023Review
- Drawbacks of Artificial Intelligence and Their Potential Solutions in the Healthcare Sector.Biomedical materials & devices (New York, N.Y.) · 2023Review
- Machine Learning Predictive Outcomes Modeling in Inflammatory Bowel Diseases.Inflammatory bowel diseases · 2022Review
- Review
- Emerging use of artificial intelligence in inflammatory bowel disease.World journal of gastroenterology · 2020Review
- A Machine Learning Model Accurately Predicts Ulcerative Colitis Activity at One Year in Patients Treated with Anti-Tumour Necrosis Factor α Agents.Medicina (Kaunas, Lithuania) · 2020Article
- Review
- Standard machine learning approaches outperform deep representation learning on phenotype prediction from transcriptomics data.BMC bioinformatics · 2020Article
- Enhancing reproducibility of gene expression analysis with known protein functional relationships: The concept of well-associated protein.PLoS computational biology · 2020Article
- Artificial Intelligence in Clinical Health Care Applications: Viewpoint.Interactive journal of medical research · 2019Article
- Robust phenotype prediction from gene expression data using differential shrinkage of co-regulated genes.Scientific reports · 2018Article
- A biological network-based regularized artificial neural network model for robust phenotype prediction from gene expression data.BMC bioinformatics · 2017Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
4 authors at 1 institution in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
motivationUnderstanding and predicting an individual's response in a clinical trial is the key to better treatments and cost-: effective medicine. Over the coming years, more and more large-scale omics datasets will become available to characterize patients with complex and heterogeneous diseases at a molecular level. Unfortunately, genetic, phenotypical and environmental variation is much higher in a human trial population than currently modeled or measured in most animal studies. In our experience, this high variability can lead to failure of trained predictors in independent studies and undermines the credibility and utility of promising high-dimensional datasets.
methodsWe propose a method that utilizes patient-level genome-wide expression data in conjunction with causal networks based on prior knowledge. Our approach determines a differential expression profile for each patient and uses a Bayesian approach to infer corresponding upstream regulators. These regulators and their corresponding posterior probabilities of activity are used in a regularized regression framework to predict response.
resultsWe validated our approach using two clinically relevant phenotypes, namely acute rejection in kidney transplantation and response to Infliximab in ulcerative colitis. To demonstrate pitfalls in translating trained predictors across independent trials, we analyze performance characteristics of our approach as well as alternative feature sets in the regression on two independent datasets for each phenotype. We show that the proposed approach is able to successfully incorporate causal prior knowledge to give robust performance estimates.
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.