Evidence map›Paper›PMID 26382192›Full record

ArticleBioinformatics (Oxford, England)2016

Component-wise gradient boosting and false discovery control in survival analysis with high-dimensional covariates.

Kevin He, Yanming Li, Ji Zhu, Hongliang Liu, Jeffrey E Lee, Christopher I Amos, Terry Hyslop, Jiashun Jin, Huazhen Lin, Qinyi Wei and 1 more

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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.

2 · The registry

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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

18 citing papers in PubMed.

  1. Article
  2. Interpretable Machine Learning for Cross-Cohort Prediction of Motor Fluctuations in Parkinson's Disease.Movement disorders : official journal of the Movement Disorder Society · 2025
    Article
  3. Article
  4. Article
  5. Article
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  7. Article
  8. Where Do We Stand in Regularization for Life Science Studies?Journal of computational biology : a journal of computational molecular cell biology · 2022
    Article
  9. Cystic fibrosis-related diabetes onset can be predicted using biomarkers measured at birth.Genetics in medicine : official journal of the American College of Medical Genetics · 2021
    Article
  10. Observational
  11. Article
  12. Article
  13. Covariance-Insured Screening.Computational statistics & data analysis · 2019
    Article
  14. Robust clinical marker identification for diabetic kidney disease with ensemble feature selection.Journal of the American Medical Informatics Association : JAMIA · 2019
    Article
  15. An exploration of ontology-based EMR data abstraction for diabetic kidney disease prediction.AMIA Joint Summits on Translational Science proceedings. AMIA Joint Summits on Translational Science · 2019
    Article
  16. False discovery control for penalized variable selections with high-dimensional covariates.Statistical applications in genetics and molecular biology · 2018
    Article
  17. Article
  18. Ensembling Variable Selectors by Stability Selection for the Cox Model.Computational intelligence and neuroscience · 2017
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors.

Kevin HeDepartment of Biostatistics and.
Yanming LiDepartment of Biostatistics and.
Ji ZhuDepartment of Statistics, University of Michigan, Ann Arbor, Michigan 48109, USA.
Hongliang LiuDepartment of Medicine, Duke University School of Medicine and Duke Cancer Institute, Duke University Medical Center, Durham, NC 27710, USA.
Jeffrey E LeeDepartment of Surgical Oncology, The University of Texas M.D. Anderson Cancer Center, Houston, TX 77030, USA.
Christopher I AmosDepartment of Community and Family Medicine, Geisel School of Medicine, Dartmouth College, Hanover, NH 03750, USA.
Terry HyslopDepartment of Biostatistics and Bioinformatics, Duke University and Duke Clinical Research Institute, Durham, NC 27710, USA.
Jiashun JinDepartment of Statistics, Carnegie Mellon University, Pittsburgh, PA 15213, USA and.
Huazhen LinCenter of Statistical Research, School of Statistics, Southwestern University of Finance and Economics, Chengdu, Sichuan 611130, China.
Qinyi WeiDepartment of Medicine, Duke University School of Medicine and Duke Cancer Institute, Duke University Medical Center, Durham, NC 27710, USA.
Yi LiDepartment of Biostatistics and.

Funding

Women's Cancer Research ProgramP30CA014236 · NCI · DUKE UNIVERSITY · PI DONNA NIEDZWIECKI · 1985 to 2026
$174.8M
Translational Engineering in Cancer (TEC)P30CA023108 · NCI · DARTMOUTH COLLEGE · PI Steven D Leach · 1985 to 2026
$91.3M
UT M.D. Anderson Cancer Center SPORE in MelanomaP50CA093459 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI GRIMM, ELIZABETH A · 2004 to 2014
$23.7M
Statistical Methods for Cancer Clinical TrialsP01CA142538 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI DAVIDIAN, MARIE, KOSOROK, MICHAEL R · 2010 to 2019
$21.3M
Genetic Predictors for DNA Repair Phenotype in CMMR01CA100264 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI WEI, QINGYI · 2004 to 2008
$1.5M
Statistical Methods for Gene Environment Interactions In Lung CancerR01CA133996 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI AMOS, CHRISTOPHER I. · 2007 to 2009
$790k
NCI NIH HHS P01 CA142538NCI NIH HHS P30CA014236NCI NIH HHS P30 CA023108NCI NIH HHS P50 CA093459NCI NIH HHS R01CA100264NCI NIH HHS R01CA133996
6 · The paper itself

Abstract

motivationTechnological advances that allow routine identification of high-dimensional risk factors have led to high demand for statistical techniques that enable full utilization of these rich sources of information for genetics studies. Variable selection for censored outcome data as well as control of false discoveries (i.e. inclusion of irrelevant variables) in the presence of high-dimensional predictors present serious challenges. This article develops a computationally feasible method based on boosting and stability selection. Specifically, we modified the component-wise gradient boosting to improve the computational feasibility and introduced random permutation in stability selection for controlling false discoveries.

resultsWe have proposed a high-dimensional variable selection method by incorporating stability selection to control false discovery. Comparisons between the proposed method and the commonly used univariate and Lasso approaches for variable selection reveal that the proposed method yields fewer false discoveries. The proposed method is applied to study the associations of 2339 common single-nucleotide polymorphisms (SNPs) with overall survival among cutaneous melanoma (CM) patients. The results have confirmed that BRCA2 pathway SNPs are likely to be associated with overall survival, as reported by previous literature. Moreover, we have identified several new Fanconi anemia (FA) pathway SNPs that are likely to modulate survival of CM patients. AVAILABILITY AND IMPLEMENTATION: The related source code and documents are freely available at https://sites.google.com/site/bestumich/issues. CONTACT: yili@umich.edu.

Indexed as

AlgorithmsBRCA2 ProteinComputer SimulationCutaneous Malignant MelanomaHumansMelanomaPolymorphism, Single NucleotideRisk FactorsSkin NeoplasmsSurvival AnalysisTime FactorsBRCA2 Protein

Identifiers

PMID26382192
PMCPMC4757968

What OpenQuestion holds

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Registered trials

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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.