Evidence map›Paper›PMID 39649094›Full record

ArticleFrontiers in genetics2024

asmbPLS: biomarker identification and patient survival prediction with multi-omics data.

Runzhi Zhang, Susmita Datta

Abstract read
In one paragraph

Article in Frontiers in genetics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Statistical consideration in nephrology research.Kidney research and clinical practice · 2025
    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

2 authors.

Runzhi ZhangDepartment of Biostatistics, University of Florida, Gainesville, FL, United States.
Susmita DattaDepartment of Biostatistics, University of Florida, Gainesville, FL, United States.

Funding

Together: Transforming and Translating Discovery to Improve HealthTL1TR001428 · NCATS · UNIVERSITY OF FLORIDA · PI MCCORMACK, WAYNE T. · 2015 to 2023
$3.9M
NCATS NIH HHS TL1 TR001428
6 · The paper itself

Abstract

Introduction: With the advancement of high-throughput studies, an increasing wealth of high-dimensional multi-omics data is being collected from the same patient cohort. However, leveraging this multi-omics data to predict survival outcomes poses a significant challenge due to its complex structure. Methods: In this article, we present a novel approach, the Adaptive Sparse Multi-Block Partial Least Squares (asmbPLS) Regression model, which introduces a dynamic assignment of penalty factors to distinct blocks within various PLS components, facilitating effective feature selection and prediction. Results: We compared the proposed method with several state-of-the-art algorithms encompassing prediction performance, feature selection and computation efficiency. We conducted comprehensive evaluations using both simulated data with various scenarios and a real dataset from the melanoma patients to validate the effectiveness and efficiency of the asmbPLS method. Additionally, we applied the lung squamous cell carcinoma (LUSC) dataset from The Cancer Genome Atlas (TCGA) to further assess the feature selection capability of asmbPLS. Discussion: The inherent nature of asmbPLS imparts it with higher sensitivity in feature selection compared to other methods. Furthermore, an R package called asmbPLS implementing this method is made publicly available.

Indexed as

feature selectionmbPLSmulti-omicsPLSpredictionsurvival

Identifiers

PMID39649094
PMCPMC11621212

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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.