Evidence map›Paper›PMID 42368974›Full record

ArticleJournal of computational and graphical statistics : a joint publication of American Statistical Association, Institute of Mathematical Statistics, Interface Foundation of North America2026

Probabilistic Joint and Individual Variation Explained (ProJIVE) for Data Integration.

Raphiel J Murden, Ganzhong Tian, Deqiang Qiu, Benjamin B Risk

Abstract read
In one paragraph

Article in Journal of computational and graphical statistics : a joint publication of American Statistical Association, Institute of Mathematical Statistics, Interface Foundation of North America, 2026. 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

4 authors.

Raphiel J MurdenDepartment of Biostatistics and Bioinformatics, Rollins School of Public Health, Emory University, Atlanta, GA.ORCID 0000-0002-6396-9105
Ganzhong TianDepartment of Biostatistics and Bioinformatics, Rollins School of Public Health, Emory University, Atlanta, GA.
Deqiang QiuDepartment of Radiology and Imaging Sciences, Emory University School of Medicine, Atlanta, GA.
Benjamin B RiskDepartment of Biostatistics and Bioinformatics, Rollins School of Public Health, Emory University, Atlanta, GA.

Funding

The Goizueta Alzheimer's Disease Research CenterP30AG066511 · NIA · EMORY UNIVERSITY · PI ALLAN I LEVEY · 2020 to 2026
$29.0M
Cerebral hemodynamic impairment in symptomatic and asymptomatic Alzheimer's DiseaseR01AG072603 · NIA · EMORY UNIVERSITY · PI Deqiang Qiu · 2022 to 2026
$3.8M
Statistical approaches to improving functional connectivity estimates with an application to autismR01MH129855 · NIMH · EMORY UNIVERSITY · PI Benjamin Brewster Risk · 2022 to 2026
$3.5M
Advancing methods for structural connectome acquisition and estimation in older adultsR21AG066970 · NIA · UNIVERSITY OF ROCHESTER · PI HEFFNER, KATHI L, LIN, FENG VANKEE · 2020 to 2020
$438k
Fast multiparametric MR imaging as early biomarkers of Alzheimer's DiseaseR21AG064405 · NIA · EMORY UNIVERSITY · PI QIU, DEQIANG · 2019 to 2020
$429k
NIA NIH HHS P30 AG066511NIA NIH HHS R01 AG072603NIA NIH HHS R21 AG064405NIA NIH HHS R21 AG066970NIMH NIH HHS R01 MH129855
6 · The paper itself

Abstract

Collecting multiple types of data on the same set of subjects is common in modern scientific applications including genomics, metabolomics, and neuroimaging. Joint and Individual Variation Explained (JIVE) seeks a low-rank approximation of the joint variation between two or more sets of features captured on common subjects and isolates this variation from that unique to each set of features. We develop an expectation-maximization (EM) algorithm to estimate a probabilistic model for the JIVE framework. The model extends probabilistic PCA to multiple datasets. Our maximum likelihood approach simultaneously estimates joint and individual components, which can lead to greater accuracy compared to other methods. We apply ProJIVE to measures of brain morphometry and cognition in Alzheimer's disease. ProJIVE learns biologically meaningful sources of variation, and the joint morphometry and cognition subject scores are strongly related to more expensive existing biomarkers. Data used in preparation of this article were obtained from the Alzheimer's Disease Neuroimaging Initiative (ADNI) database. Code to reproduce the analysis is available at https://github.com/thebrisklab/ProJIVE.

Indexed as

ADNIAlzheimer’s DiseaseJIVEMulti-block data analysisMultimodal data analysisProbabilistic PCA

Identifiers

PMID42368974
PMCPMC13308631

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.