Evidence map›Paper›PMID 24530838›Full record

ReviewNeuroImage2014

Sparse representation based biomarker selection for schizophrenia with integrated analysis of fMRI and SNPs.

Hongbao Cao, Junbo Duan, Dongdong Lin, Yin Yao Shugart, Vince Calhoun, Yu-Ping Wang

Abstract readReview
In one paragraph

Review in NeuroImage, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing 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

26 citing papers in PubMed.

  1. Article
  2. Review
  3. Brain imaging and behavior · 2023
    Article
  4. Article
  5. Brain Functional Connectivity Analysis via Graphical Deep Learning.IEEE transactions on bio-medical engineering · 2022
    Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. A Curated Target Gene Pool Assisting Early Disease Prediction and Patient-Specific Treatment for Small Cell Lung Cancer.Journal of computational biology : a journal of computational molecular cell biology · 2018
    Article
  16. Article
  17. Review
  18. Article
  19. Article
  20. 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

6 authors.

Hongbao CaoUnit on Statistical Genomics, Intramural Program of Research, National Institute of Mental Health, NIH, Bethesda, 20852, USA.
Junbo DuanDepartment of Biomedical Engineering, Tulane University, New Orleans, LA, USA; Department of Biostatistics & Bioinformatics, Tulane University, New Orleans, LA, USA.
Dongdong LinDepartment of Biomedical Engineering, Tulane University, New Orleans, LA, USA.
Yin Yao ShugartUnit on Statistical Genomics, Intramural Program of Research, National Institute of Mental Health, NIH, Bethesda, 20852, USA.
Vince CalhounThe Mind Research Network, Albuquerque, NM, USA; Department of Electrical and Computer Engineering at the University of New Mexico, Albuquerque, NM, USA.
Yu-Ping WangDepartment of Biomedical Engineering, Tulane University, New Orleans, LA, USA; Department of Biostatistics & Bioinformatics, Tulane University, New Orleans, LA, USA. Electronic address: wyp@tulane.edu.

Funding

Multivariate methods for identifying multitask/multimodal brain imaging biomarkersR01EB006841 · NIBIB · THE MIND RESEARCH NETWORK · PI VINCE D CALHOUN, Sergey Plis · 2007 to 2026
$9.8M
Informed Data-Driven Fusion of Behavior, Brain Function, and GenesR01EB005846 · NIBIB · THE MIND RESEARCH NETWORK · PI CALHOUN, VINCE D · 2005 to 2016
$5.5M
Unified multivariate data-driven solutions for static and dynamic brain connectivityR01EB020407 · NIBIB · THE MIND RESEARCH NETWORK · PI ADALI, TULAY, CALHOUN, VINCE D · 2015 to 2018
$2.7M
Developing new statisical methods to detect variants involved in complex diseaseZIAMH002929 · NIMH · NATIONAL INSTITUTE OF MENTAL HEALTH · PI YAO, YIN · 2011 to 2016
$2.6M
Integration of brain imaging with genomic and epigenomic dataR01MH104680 · NIMH · TULANE UNIVERSITY OF LOUISIANA · PI CALHOUN, VINCE D, DENG, HONG-WEN · 2014 to 2017
$2.1M
Integration of multiscale genomic data for comprehensive analysis of complex diseR01GM109068 · NIGMS · TULANE UNIVERSITY OF LOUISIANA · PI WANG, YU-PING · 2014 to 2018
$1.6M
Developing Stats Methods to Detect Rare Genetics Variants in Human PedigreesZIAMH002930 · NIMH · NATIONAL INSTITUTE OF MENTAL HEALTH · PI YAO, YIN · 2011 to 2016
$1.6M
Integrating fMRI and Next-Generation-Sequencing Data to Identify Schizophrenia BiomarkersZIAMH002934 · NIMH · NATIONAL INSTITUTE OF MENTAL HEALTH · PI YAO, YIN · 2013 to 2016
$638k
A New Paradigm for Integrated Analysis of Multiscale Genomic Imaging DatasetsR21LM010042 · NLM · UNIVERSITY OF MISSOURI KANSAS CITY · PI WANG, YU-PING · 2009 to 2010
$406k
Intramural NIH HHSNIBIB NIH HHS R01 EB005846NIBIB NIH HHS R01 EB006841NIBIB NIH HHS R01 EB020407NIGMS NIH HHS R01 GM109068NIMH NIH HHS MH002930-03NIMH NIH HHS R01 MH104680NIMH NIH HHS R01MH104680NLM NIH HHS R21 LM010042
6 · The paper itself

Abstract

Integrative analysis of multiple data types can take advantage of their complementary information and therefore may provide higher power to identify potential biomarkers that would be missed using individual data analysis. Due to different natures of diverse data modality, data integration is challenging. Here we address the data integration problem by developing a generalized sparse model (GSM) using weighting factors to integrate multi-modality data for biomarker selection. As an example, we applied the GSM model to a joint analysis of two types of schizophrenia data sets: 759,075 SNPs and 153,594 functional magnetic resonance imaging (fMRI) voxels in 208 subjects (92 cases/116 controls). To solve this small-sample-large-variable problem, we developed a novel sparse representation based variable selection (SRVS) algorithm, with the primary aim to identify biomarkers associated with schizophrenia. To validate the effectiveness of the selected variables, we performed multivariate classification followed by a ten-fold cross validation. We compared our proposed SRVS algorithm with an earlier sparse model based variable selection algorithm for integrated analysis. In addition, we compared with the traditional statistics method for uni-variant data analysis (Chi-squared test for SNP data and ANOVA for fMRI data). Results showed that our proposed SRVS method can identify novel biomarkers that show stronger capability in distinguishing schizophrenia patients from healthy controls. Moreover, better classification ratios were achieved using biomarkers from both types of data, suggesting the importance of integrative analysis.

Indexed as

Magnetic Resonance ImagingPolymorphism, Single NucleotideAdultAlgorithmsBiomarkersFemaleHumansModels, StatisticalSchizophreniaBiomarkersfMRISchizophreniaSNPSparse representationsVariable selection

Identifiers

PMID24530838
PMCPMC4130811

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.