Evidence map›Paper›PMID 26756854›Full record

ArticleStatistics in medicine2016

Integrative and regularized principal component analysis of multiple sources of data.

Binghui Liu, Xiaotong Shen, Wei Pan

Abstract read
In one paragraph

Article in Statistics in medicine, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Fast Fusion Clustering via Double Random Projection.Entropy (Basel, Switzerland) · 2024
    Article
  2. Robust integrative biclustering for multi-view data.Statistical methods in medical research · 2022
    Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. A New Algorithm and Theory for Penalized Regression-based Clustering.Journal of machine learning research : JMLR · 2016
    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

3 authors.

Binghui LiuSchool of Mathematics and Statistics, Northeast Normal University, Changchun, 130024, Jilin Province, China.
Xiaotong ShenSchool of Statistics, University of Minnesota, 224 Church St. S.E., Minneapolis, 55455, MN, U.S.A.
Wei PanDivision of Biostatistics, University of Minnesota, 420 Delaware St. S.E., Minneapolis, 55455, MN, U.S.A.

Funding

Powerful Inference and Prediction for Genetic AssociationR01HL105397 · NHLBI · UNIVERSITY OF MINNESOTA · PI PAN, WEI, SHEN, XIAOTONG TOM · 2011 to 2018
$2.9M
New Machine Learning Tools for Biomedical DataR01GM081535 · NIGMS · UNIVERSITY OF MINNESOTA · PI PAN, WEI, SHEN, XIAOTONG TOM · 2007 to 2014
$2.2M
Statistical Methods for Genomic DataR01GM113250 · NIGMS · UNIVERSITY OF MINNESOTA · PI PAN, WEI · 2014 to 2017
$702k
NHLBI NIH HHS R01 HL105397NIGMS NIH HHS R01 GM081535NIGMS NIH HHS R01 GM113250
6 · The paper itself

Abstract

Integration of data of disparate types has become increasingly important to enhancing the power for new discoveries by combining complementary strengths of multiple types of data. One application is to uncover tumor subtypes in human cancer research in which multiple types of genomic data are integrated, including gene expression, DNA copy number, and DNA methylation data. In spite of their successes, existing approaches based on joint latent variable models require stringent distributional assumptions and may suffer from unbalanced scales (or units) of different types of data and non-scalability of the corresponding algorithms. In this paper, we propose an alternative based on integrative and regularized principal component analysis, which is distribution-free, computationally efficient, and robust against unbalanced scales. The new method performs dimension reduction simultaneously on multiple types of data, seeking data-adaptive sparsity and scaling. As a result, in addition to feature selection for each type of data, integrative clustering is achieved. Numerically, the proposed method compares favorably against its competitors in terms of accuracy (in identifying hidden clusters), computational efficiency, and robustness against unbalanced scales. In particular, compared with a popular method, the new method was competitive in identifying tumor subtypes associated with distinct patient survival patterns when applied to a combined analysis of DNA copy number, mRNA expression, and DNA methylation data in a glioblastoma multiforme study. Copyright © 2016 John Wiley & Sons, Ltd.

Indexed as

Data Interpretation, StatisticalAlgorithmsCluster AnalysisDNA Copy Number VariationsDNA MethylationGene Expression Regulation, NeoplasticGlioblastomaHumansModels, StatisticalPrincipal Component Analysisintegrative clusteringPCAtumor subtypes

Identifiers

PMID26756854
PMCPMC4853304

What OpenQuestion holds

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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.