Evidence map›Paper›PMID 27862229›Full record

ArticleGenetic epidemiology2017

Sparse multivariate factor analysis regression models and its applications to integrative genomics analysis.

Yan Zhou, Pei Wang, Xianlong Wang, Ji Zhu, Peter X-K Song

Open access · bronzeAbstract read
In one paragraph

Article in Genetic epidemiology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.5field-weighted citation impact, top 27% of its field
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

6 citing papers in PubMed, 9 citations in OpenAlex.

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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

5 authors at 4 institutions in 1 country.

Yan ZhouMerck & Co, North Wales, PA, USA.
Pei WangIcahn School of Medicine at Mount Sinai, New York, NY, USA.
Xianlong WangFred Hutchinson Cancer Research Center, Seattle, WA, USA.
Ji ZhuUniversity of Michigan, Ann Arbor, MI, USA.
Peter X-K SongUniversity of Michigan, Ann Arbor, MI, USA.
University of Michigan–Ann Arbor · USFred Hutch Cancer Center · USIcahn School of Medicine at Mount Sinai · USMerck & Co., Inc., Rahway, NJ, USA (United States) · US

Funding

Proteo-genomic Discovery, Prioritization and Verification of Cancer BiomarkersU24CA160034 · NCI · BROAD INSTITUTE, INC. · PI CARR, STEVEN A, PAULOVICH, AMANDA G · 2011 to 2016
$16.2M
Use of Biomarkers in Diagnosis, Prognosis, Risk Prediction and Early Detection ofP01CA053996 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI PRENTICE, ROSS L · 1991 to 2015
$9.4M
Project 3: Developmental Exposures and Diet: Epigenetics of Metabolic SyndromeP01ES022844 · NIEHS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI PADMANABHAN, VASANTHA, PETERSON, KAREN EILEEN · 2013 to 2018
$3.9M
Integrative multivariate association and genomic analysesR01GM108711 · NIGMS · UNIVERSITY OF CHICAGO · PI CHEN, LIN · 2014 to 2022
$3.1M
Statistical Methods for Integrative Analysis of Genomics and Proteomics DataR01GM082802 · NIGMS · FRED HUTCHINSON CANCER RESEARCH CENTER · PI WANG, PEI · 2008 to 2012
$1.4M
Statistical Methods to Assess Early Life Environmental Exposures on Child HealthR01ES024732 · NIEHS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI SONG, PETER XUEKUN · 2015 to 2018
$1.3M
NCI NIH HHS P01 CA053996NCI NIH HHS U24 CA160034NIEHS NIH HHS P01 ES022844NIEHS NIH HHS R01 ES024732NIGMS NIH HHS R01 GM082802NIGMS NIH HHS R01 GM108711
6 · The paper itself

Abstract

The multivariate regression model is a useful tool to explore complex associations between two kinds of molecular markers, which enables the understanding of the biological pathways underlying disease etiology. For a set of correlated response variables, accounting for such dependency can increase statistical power. Motivated by integrative genomic data analyses, we propose a new methodology-sparse multivariate factor analysis regression model (smFARM), in which correlations of response variables are assumed to follow a factor analysis model with latent factors. This proposed method not only allows us to address the challenge that the number of association parameters is larger than the sample size, but also to adjust for unobserved genetic and/or nongenetic factors that potentially conceal the underlying response-predictor associations. The proposed smFARM is implemented by the EM algorithm and the blockwise coordinate descent algorithm. The proposed methodology is evaluated and compared to the existing methods through extensive simulation studies. Our results show that accounting for latent factors through the proposed smFARM can improve sensitivity of signal detection and accuracy of sparse association map estimation. We illustrate smFARM by two integrative genomics analysis examples, a breast cancer dataset, and an ovarian cancer dataset, to assess the relationship between DNA copy numbers and gene expression arrays to understand genetic regulatory patterns relevant to the disease. We identify two trans-hub regions: one in cytoband 17q12 whose amplification influences the RNA expression levels of important breast cancer genes, and the other in cytoband 9q21.32-33, which is associated with chemoresistance in ovarian cancer.

Indexed as

Factor Analysis, StatisticalMultivariate AnalysisAlgorithmsBiomarkers, TumorBreast NeoplasmsFemaleGenomicsHumansModels, GeneticOvarian NeoplasmsBiomarkers, TumorEM-blockwise coordinate descenthigh-dimensional datalatent factorsregularization

Identifiers

PMID27862229
PMCPMC5154917
OpenAlexW2555995761

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.