ArticleStatistics in biosciences2017
Prediction-Oriented Marker Selection (PROMISE): With Application to High-Dimensional Regression.
Article in Statistics in biosciences, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.
What it found
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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
6 citing papers in PubMed.
- Prediction-oriented prognostic biomarker discovery with survival machine learning methods.NAR genomics and bioinformatics · 2023Article
- Statistical and Machine Learning Methods for Discovering Prognostic Biomarkers for Survival Outcomes.Methods in molecular biology (Clifton, N.J.) · 2023Article
- Measuring individual benefits of psychiatric treatment using longitudinal binary outcomes: Application to antipsychotic benefits in non-cannabis and cannabis users.Journal of biopharmaceutical statistics · 2020Article
- Collective effects of long-range DNA methylations predict gene expressions and estimate phenotypes in cancer.Scientific reports · 2020Article
- Germinal Immunogenetics predict treatment outcome for PD-1/PD-L1 checkpoint inhibitors.Investigational new drugs · 2020Article
- 3' UTR shortening represses tumor-suppressor genes in trans by disrupting ceRNA crosstalk.Nature genetics · 2018Article
Corrections and comments
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Authors and funding
3 authors.
Funding
Abstract
In personalized medicine, biomarkers are used to select therapies with the highest likelihood of success based on an individual patient's biomarker/genomic profile. Two goals are to choose important biomarkers that accurately predict treatment outcomes and to cull unimportant biomarkers to reduce the cost of biological and clinical verifications. These goals are challenging due to the high dimensionality of genomic data. Variable selection methods based on penalized regression (e.g., the lasso and elastic net) have yielded promising results. However, selecting the right amount of penalization is critical to simultaneously achieving these two goals. Standard approaches based on cross-validation (CV) typically provide high prediction accuracy with high true positive rates but at the cost of too many false positives. Alternatively, stability selection (SS) controls the number of false positives, but at the cost of yielding too few true positives. To circumvent these issues, we propose prediction-oriented marker selection (PROMISE), which combines SS with CV to conflate the advantages of both methods. Our application of PROMISE with the lasso and elastic net in data analysis shows that, compared to CV, PROMISE produces sparse solutions, few false positives, and small type I + type II error, and maintains good prediction accuracy, with a marginal decrease in the true positive rates. Compared to SS, PROMISE offers better prediction accuracy and true positive rates. In summary, PROMISE can be applied in many fields to select regularization parameters when the goals are to minimize false positives and maximize prediction accuracy.
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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.