Evidence map›Paper›PMID 39897528›Full record

ArticleFrontiers in systems biology2024

A robust ensemble feature selection approach to prioritize genes associated with survival outcome in high-dimensional gene expression data.

Phi Le, Xingyue Gong, Leah Ung, Hai Yang, Bridget P Keenan, Li Zhang, Tao He

Abstract read
In one paragraph

Article in Frontiers in systems biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. 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

7 authors.

Phi LeDivision of Hematology/Oncology, Department of Medicine, University of California, San Francisco, San Francisco, CA, United States.
Xingyue GongDepartment of Physiological Nursing, School of Nursing, University of California, San Francisco, San Francisco, CA, United States.
Leah UngDivision of Hematology/Oncology, Department of Medicine, University of California, San Francisco, San Francisco, CA, United States.
Hai YangDivision of Hematology/Oncology, Department of Medicine, University of California, San Francisco, San Francisco, CA, United States.
Bridget P KeenanDivision of Hematology/Oncology, Department of Medicine, University of California, San Francisco, San Francisco, CA, United States.
Li ZhangDivision of Hematology/Oncology, Department of Medicine, University of California, San Francisco, San Francisco, CA, United States.
Tao HeDepartment of Mathematics, San Francisco State University, San Francisco, CA, United States.

Funding

UCSF Paul Calabresi K12 Career Development Program in Clinical OncologyK12CA260225 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI BERGSLAND, EMILY K, BIVONA, TREVER G · 2021 to 2025
$2.6M
Investigation of the landscape of immunosequencing and its clinical relevance through novel immunoinformatic approachesR01LM013763 · NLM · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI ZHANG, LI · 2022 to 2025
$1.4M
Computational approaches to unravel immune receptor sequencing for cancer immunotherapyR21CA264381 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI ZHANG, LI · 2021 to 2022
$384k
NCI NIH HHS K12 CA260225NCI NIH HHS R21 CA264381NLM NIH HHS R01 LM013763
6 · The paper itself

Abstract

Exploring features associated with the clinical outcome of interest is a rapidly advancing area of research. However, with contemporary sequencing technologies capable of identifying over thousands of genes per sample, there is a challenge in constructing efficient prediction models that balance accuracy and resource utilization. To address this challenge, researchers have developed feature selection methods to enhance performance, reduce overfitting, and ensure resource efficiency. However, applying feature selection models to survival analysis, particularly in clinical datasets characterized by substantial censoring and limited sample sizes, introduces unique challenges. We propose a robust ensemble feature selection approach integrated with group Lasso to identify compelling features and evaluate its performance in predicting survival outcomes. Our approach consistently outperforms established models across various criteria through extensive simulations, demonstrating low false discovery rates, high sensitivity, and high stability. Furthermore, we applied the approach to a colorectal cancer dataset from The Cancer Genome Atlas, showcasing its effectiveness by generating a composite score based on the selected genes to correctly distinguish different subtypes of the patients. In summary, our proposed approach excels in selecting impactful features from high-dimensional data, yielding better outcomes compared to contemporary state-of-the-art models.

Indexed as

colorectal cancerensemble feature selectiongroup lassohigh-dimensional datapseudo variablestime-to-event outcome

Identifiers

PMID39897528
PMCPMC11786965

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.