Evidence map›Paper›PMID 22078224›Full record

ArticleBMC bioinformatics2011

Consistent Differential Expression Pattern (CDEP) on microarray to identify genes related to metastatic behavior.

Lam C Tsoi, Tingting Qin, Elizabeth H Slate, W Jim Zheng

Abstract read
In one paragraph

Article in BMC bioinformatics, 2011. 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
–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

6 citing papers in PubMed.

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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

4 authors.

Lam C TsoiDepartment of Biochemistry and Molecular Biology, Medical University of South Carolina, 135 Cannon St, Charleston, SC 29425, USA.
Tingting Qin
Elizabeth H Slate
W Jim Zheng

Funding

THE ROLE OF LACTOSYLCERAMIDE IN RENAL AGING AND DISEASEP20RR017677 · NCRR · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI MAO, CUNGUI · 2002 to 2011
$23.4M
THE ROLE OF THE RNA BINDING PROTEIN LA IN ORAL TUMOR BIOLOGYP20RR017696 · NCRR · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI SOMMER, GUNHILD · 2002 to 2011
$20.7M
Modeling and Analysis of Yeast Sphingolipid MetabolismR01GM063265 · NIGMS · STATE UNIVERSITY NEW YORK STONY BROOK · PI HANNUN, YUSUF AWNI · 2001 to 2013
$3.4M
Training of Toolmakers for Bio-Medical Informatics (TTB*T15LM007438 · NLM · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI LU, XINGHUA · 2002 to 2008
$1.6M
Biostatistics Training for Basic Biomedical ResearchT32GM074934 · NIGMS · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI RAMAKRISHNAN, VISWANATHAN · 2005 to 2012
$1.1M
Logic Forest: A Statistical Method for Biomarker DiscoveryR03CA137805 · NCI · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI SLATE, ELIZABETH H. · 2008 to 2009
$146k
NCI NIH HHS R03CA137805NCRR NIH HHS 5P20RR017677-10NCRR NIH HHS P20 RR017677-10NCRR NIH HHS P20RR017696NCRR NIH HHS P20 RR017696-05NIGMS NIH HHS R01GM063265-09S1NIGMS NIH HHS T32GM074934 07NLM NIH HHS 5-T15-LM007438-02
6 · The paper itself

Abstract

backgroundTo utilize the large volume of gene expression information generated from different microarray experiments, several meta-analysis techniques have been developed. Despite these efforts, there remain significant challenges to effectively increasing the statistical power and decreasing the Type I error rate while pooling the heterogeneous datasets from public resources. The objective of this study is to develop a novel meta-analysis approach, Consistent Differential Expression Pattern (CDEP), to identify genes with common differential expression patterns across different datasets.

resultsWe combined False Discovery Rate (FDR) estimation and the non-parametric RankProd approach to estimate the Type I error rate in each microarray dataset of the meta-analysis. These Type I error rates from all datasets were then used to identify genes with common differential expression patterns. Our simulation study showed that CDEP achieved higher statistical power and maintained low Type I error rate when compared with two recently proposed meta-analysis approaches. We applied CDEP to analyze microarray data from different laboratories that compared transcription profiles between metastatic and primary cancer of different types. Many genes identified as differentially expressed consistently across different cancer types are in pathways related to metastatic behavior, such as ECM-receptor interaction, focal adhesion, and blood vessel development. We also identified novel genes such as AMIGO2, Gem, and CXCL11 that have not been shown to associate with, but may play roles in, metastasis.

conclusionsCDEP is a flexible approach that borrows information from each dataset in a meta-analysis in order to identify genes being differentially expressed consistently. We have shown that CDEP can gain higher statistical power than other existing approaches under a variety of settings considered in the simulation study, suggesting its robustness and insensitivity to data variation commonly associated with microarray experiments. AVAILABILITY: CDEP is implemented in R and freely available at: http://genomebioinfo.musc.edu/CDEP/. CONTACT: zhengw@musc.edu.

Indexed as

Neoplasm MetastasisGene Expression ProfilingGene Expression Regulation, NeoplasticHumansMeta-Analysis as TopicOligonucleotide Array Sequence Analysis

Identifiers

PMID22078224
PMCPMC3251006

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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.