Evidence map›Paper›PMID 39416165›Full record

ArticlebioRxiv : the preprint server for biology2024

High-dimensional Biomarker Identification for Scalable and Interpretable Disease Prediction via Machine Learning Models.

Yifan Dai, Fei Zou, Baiming Zou

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

3 authors.

Yifan DaiDepartment of Biostatistics, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.
Fei ZouDepartment of Biostatistics, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.
Baiming ZouDepartment of Biostatistics, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.

Funding

Robust Computational and Data Analytic Tools for In-depth Understanding Postoperative Pain Mechanism with Enhanced Pain Management and Clinical Decision MakingR01LM014407 · NLM · UNIV OF NORTH CAROLINA CHAPEL HILL · PI Baiming Zou · 2024 to 2026
$1.4M
Novel Deep Learning Tools for Clinical Decision Support in Postoperative Pain ManagementR56LM013784 · NLM · UNIV OF NORTH CAROLINA CHAPEL HILL · PI ZOU, BAIMING · 2022 to 2023
$832k
NLM NIH HHS R01 LM014407NLM NIH HHS R56 LM013784
6 · The paper itself

Abstract

Omics data generated from high-throughput technologies and clinical features jointly impact many complex human diseases. Identifying key biomarkers and clinical risk factors is essential for understanding disease mechanisms and advancing early disease diagnosis and precision medicine. However, the high-dimensionality and intricate associations between disease outcomes and omics profiles present significant analytical challenges. To address these, we propose an ensemble data-driven biomarker identification tool, Hybrid Feature Screening (HFS), to construct a candidate feature set for downstream advanced machine learning models. The pre-screened candidate features from HFS are further refined using a computationally efficient permutation-based feature importance test, forming the comprehensive High-dimensional Feature Importance Test (HiFIT) framework. Through extensive numerical simulations and real-world applications, we demonstrate HiFIT's superior performance in both outcome prediction and feature importance identification. An R package implementing HiFIT is available on GitHub (https://github.com/BZou-lab/HiFIT).

Indexed as

Deep learningFeature prescreeningGenomics data integrationModel interpretationNonlinear association

Identifiers

PMID39416165
PMCPMC11482776

What OpenQuestion holds

Textmetadata
LicenceCC BY
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Registered trials

None linked

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.