Evidence map›Paper›PMID 39131398›Full record

ArticlebioRxiv : the preprint server for biology2024

Bootstrap Evaluation of Association Matrices (BEAM) for Integrating Multiple Omics Profiles with Multiple Outcomes.

Anna Eames Seffernick, Xueyuan Cao, Cheng Cheng, Wenjian Yang, Robert J Autry, Jun J Yang, Ching-Hon Pui, David T Teachey, Jatinder K Lamba, Charles G Mullighan and 1 more

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

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.

Anna Eames SeffernickDepartment of Biostatistics, St. Jude Children's Research Hospital, Memphis, TN, USA.ORCID 0000-0003-0848-4604
Xueyuan CaoDepartment of Health Promotion and Disease Prevention, University of Tennessee Health Science Center, Memphis, TN, USA.
Cheng ChengDepartment of Biostatistics, St. Jude Children's Research Hospital, Memphis, TN, USA.
Wenjian YangDepartment of Pharmacy & Pharmaceutical Services, St. Jude Children's Research Hospital, Memphis, TN, USA.
Robert J AutryHopp Children's Cancer Center Heidelberg (KiTZ), Heidelberg, Germany.
Jun J YangDepartment of Pharmacy & Pharmaceutical Services, St. Jude Children's Research Hospital, Memphis, TN, USA.
Ching-Hon PuiHematological Malignancies Program, St. Jude Children's Research Hospital, Memphis, TN, USA.
David T TeacheyPerelman School of Medicine at the University of Pennsylvania, Philadelphia, PA, USA.
Jatinder K LambaDepartment of Pharmacotherapy and Translational Research, University of Florida College of Pharmacy, Gainesville, FL, USA.
Charles G MullighanHematological Malignancies Program, St. Jude Children's Research Hospital, Memphis, TN, USA.ORCID 0000-0002-1871-1850
Stanley B PoundsDepartment of Biostatistics, St. Jude Children's Research Hospital, Memphis, TN, USA.

Funding

Viral Vector Technology (VVTSR)P30CA021765 · NCI · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI CHARLES ROBERTS · 1985 to 2026
$166.9M
Pharmacogenomics of Ara-C in AMLR01CA132946 · NCI · UNIVERSITY OF MINNESOTA · PI LAMBA, JATINDER K., POUNDS, STANLEY BARRETT · 2008 to 2025
$5.3M
Integrated Systems Biology of Pediatric AMLR01CA270120 · NCI · UNIVERSITY OF FLORIDA · PI Jatinder K. Lamba, Stanley Barrett Pounds · 2023 to 2026
$2.7M
Childhood Hematological Malignancies Training ProgramT32CA236748 · NCI · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI Charles G Mullighan · 2019 to 2026
$2.0M
NCI NIH HHS P30 CA021765NCI NIH HHS R01 CA132946NCI NIH HHS R01 CA270120NCI NIH HHS T32 CA236748
6 · The paper itself

Abstract

Motivation: Large datasets containing multiple clinical and omics measurements for each subject motivate the development of new statistical methods to integrate these data to advance scientific discovery. Model: We propose bootstrap evaluation of association matrices (BEAM), which integrates multiple omics profiles with multiple clinical endpoints. BEAM associates a set omic features with clinical endpoints via regression models and then uses bootstrap resampling to determine statistical significance of the set. Unlike existing methods, BEAM uniquely accommodates an arbitrary number of omic profiles and endpoints. Results: In simulations, BEAM performed similarly to the theoretically best simple test and outperformed other integrated analysis methods. In an example pediatric leukemia application, BEAM identified several genes with biological relevance established by a CRISPR assay that had been missed by univariate screens and other integrated analysis methods. Thus, BEAM is a powerful, flexible, and robust tool to identify genes for further laboratory and/or clinical research evaluation. Availability: Source code, documentation, and a vignette for BEAM are available on GitHub at: https://github.com/annaSeffernick/BEAMR. The R package is available from CRAN at: https://cran.r-project.org/package=BEAMR. Contact: Stanley.Pounds@stjude.org. Supplementary Information: Supplementary data are available at the journal's website.

Identifiers

PMID39131398
PMCPMC11312528

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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.