Evidence map›Paper›PMID 40740430›Full record

ArticleThe annals of applied statistics2024

OUTCOME-GUIDED DISEASE SUBTYPING BY GENERATIVE MODEL AND WEIGHTED JOINT LIKELIHOOD IN TRANSCRIPTOMIC APPLICATIONS.

Yujia Li, Peng Liu, Wenjia Wang, Wei Zong, Yusi Fang, Zhao Ren, Lu Tang, Juan C Celedón, Steffi Oesterreich, George C Tseng

Abstract read
In one paragraph

Article in The annals of applied statistics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

10 authors.

Yujia LiUniversity of Pittsburgh.
Peng LiuUniversity of Pittsburgh.
Wenjia WangUniversity of Pittsburgh.
Wei ZongUniversity of Pittsburgh.
Yusi FangUniversity of Pittsburgh.
Zhao RenUniversity of Pittsburgh.
Lu TangUniversity of Pittsburgh.
Juan C CeledónUniversity of Pittsburgh.
Steffi OesterreichUniversity of Pittsburgh.
George C TsengUniversity of Pittsburgh.

Funding

Disease subtyping guided by clinical phenotype for precision medicineR01LM014142 · NLM · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI George C. Tseng · 2023 to 2026
$1.2M
Congruence of mouse model to human in transcriptomic responseR21LM012752 · NLM · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI TSENG, GEORGE C. · 2018 to 2019
$370k
NLM NIH HHS R01 LM014142NLM NIH HHS R21 LM012752
6 · The paper itself

Abstract

With advances in high-throughput technology, molecular disease subtyping by high-dimensional omics data has been recognized as an effective approach for identifying subtypes of complex diseases with distinct disease mechanisms and prognoses. Conventional cluster analysis takes omics data as input and generates patient clusters with similar gene expression pattern. The omics data, however, usually contain multi-faceted cluster structures that can be defined by different sets of gene. If the gene set associated with irrelevant clinical variables (e.g., sex or age) dominates the clustering process, the resulting clusters may not capture clinically meaningful disease subtypes. This motivates the development of a clustering framework with guidance from a pre-specified disease outcome, such as lung function measurement or survival, in this paper. We propose two disease subtyping methods by omics data with outcome guidance using a generative model or a weighted joint likelihood. Both methods connect an outcome association model and a disease subtyping model by a latent variable of cluster labels. Compared to the generative model, weighted joint likelihood contains a data-driven weight parameter to balance the likelihood contributions from outcome association and gene cluster separation, which improves generalizability in independent validation but requires heavier computing. Extensive simulations and two real applications in lung disease and triple-negative breast cancer demonstrate superior disease subtyping performance of the outcome-guided clustering methods in terms of disease subtyping accuracy, gene selection and outcome association. Unlike existing clustering methods, the outcome-guided disease subtyping framework creates a new precision medicine paradigm to directly identify patient subgroups with clinical association.

Indexed as

disease subtypinggenerative modelhigh-dimensional cluster analysisomics dataweighted joint likelihood

Identifiers

PMID40740430
PMCPMC12309773

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

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.