Evidence map›Paper›PMID 39541190›Full record

ArticleBriefings in bioinformatics2024

Molecular group and correlation guided structural learning for multi-phenotype prediction.

Xueping Zhou, Manqi Cai, Molin Yue, Juan C Celedón, Jiebiao Wang, Ying Ding, Wei Chen, Yanming Li

Abstract read
In one paragraph

Article in Briefings in bioinformatics, 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

8 authors.

Xueping ZhouDepartment of Biostatistics, University of Pittsburgh, Pittsburgh, PA 15216, United States.
Manqi CaiDepartment of Biostatistics, University of Pittsburgh, Pittsburgh, PA 15216, United States.
Molin YueDepartment of Biostatistics, University of Pittsburgh, Pittsburgh, PA 15216, United States.
Juan C CeledónDepartment of Pediatrics, University of Pittsburgh Medical Center Children's Hospital of Pittsburgh, Pittsburgh, PA 15224, United States.
Jiebiao WangDepartment of Biostatistics, University of Pittsburgh, Pittsburgh, PA 15216, United States.
Ying DingDepartment of Biostatistics, University of Pittsburgh, Pittsburgh, PA 15216, United States.
Wei ChenDepartment of Pediatrics, University of Pittsburgh Medical Center Children's Hospital of Pittsburgh, Pittsburgh, PA 15224, United States.
Yanming LiDepartment of Biostatistics & Data Science, University of Kansas Medical Center, Kansas, KS 66160, United States.

Funding

Epigenetic Variation and Childhood Asthma in Puerto RicansR01HL117191 · NHLBI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI CELEDON, JUAN CARLOS · 2013 to 2020
$5.8M
High-Throughput Computing for Genomics and Bioinformatics ResearchS10OD028483 · OD · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI LEE, ADRIAN V · 2021 to 2021
$574k
Multi-omics Analysis of Childhood Asthma in HispanicsR21HL150431 · NHLBI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI CELEDON, JUAN CARLOS, CHEN, WEI · 2020 to 2021
$235k
National Science Foundation 2225775NHLBI NIH HHS R01 HL117191NHLBI NIH HHS R21 HL150431NIH HHS R01HL117191NIH HHS S10 OD028483NIH HHS S10OD028483NSF OAC-2117681
6 · The paper itself

Abstract

We propose a supervised learning bioinformatics tool, Biological gRoup guIded muLtivariate muLtiple lIneAr regression with peNalizaTion (Brilliant), designed for feature selection and outcome prediction in genomic data with multi-phenotypic responses. Brilliant specifically incorporates genome and/or phenotype grouping structures, as well as phenotype correlation structures, in feature selection, effect estimation, and outcome prediction under a penalized multi-response linear regression model. Extensive simulations demonstrate its superior performance compared to competing methods. We applied Brilliant to two omics studies. In the first study, we identified novel association signals between multivariate gene expressions and high-dimensional DNA methylation profiles, providing biological insights for the baseline CpG-to-gene regulation patterns in a Puerto Rican children asthma cohort. The second study focused on cell-type deconvolution prediction using high-dimensional gene expression profiles. Using Brilliant, we improved the accuracy for cell-type fraction prediction and identified novel cell-type signature genes.

Indexed as

Computational BiologyPhenotypeAsthmaCpG IslandsDNA MethylationGenomicsHumansLinear Modelsassociation studycell-type deconvolutionDNA methylationfeature selectiongenomic grouping structuremulti-type prediction

Identifiers

PMID39541190
PMCPMC11562839

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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.