Evidence map›Paper›PMID 15774002›Full record

ArticleBMC bioinformatics2005

Towards precise classification of cancers based on robust gene functional expression profiles.

Zheng Guo, Tianwen Zhang, Xia Li, Qi Wang, Jianzhen Xu, Hui Yu, Jing Zhu, Haiyun Wang, Chenguang Wang, Eric J Topol and 2 more

Abstract read
In one paragraph

Article in BMC bioinformatics, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 73 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
73citing papers in PubMed, 1 pooled it
–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

73 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Article
  4. Knowledge-Informed Machine Learning for Cancer Diagnosis and Prognosis: A Review.IEEE transactions on automation science and engineering : a publication of the IEEE Robotics and Automation Society · 2025
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  9. Pathway expression analysis.Scientific reports · 2022
    Article
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  12. Review
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  15. Review
  16. Article
  17. Article
  18. Review
  19. Article
  20. PIMKL: Pathway-Induced Multiple Kernel Learning.NPJ systems biology and applications · 2019
    Article

13 more citing papers are in PubMed but not listed here.

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

12 authors.

Zheng GuoDepartment of Computer Science, Harbin Institute of Technology, Harbin 150001, China. guoz@ems.hrbmu.edu.cn
Tianwen Zhang
Xia Li
Qi Wang
Jianzhen Xu
Hui Yu
Jing Zhu
Haiyun Wang
Chenguang Wang
Eric J Topol
Qing Wang
Shaoqi Rao

Funding

Molecular Mechanisms of Cardiac ArrhythmiasR01HL066251 · NHLBI · CLEVELAND CLINIC LERNER COL/MED-CWRU · PI WANG, QING KENNETH · 2002 to 2005
$1.7M
NHLBI NIH HHS R01 HL066251
6 · The paper itself

Abstract

backgroundDevelopment of robust and efficient methods for analyzing and interpreting high dimension gene expression profiles continues to be a focus in computational biology. The accumulated experiment evidence supports the assumption that genes express and perform their functions in modular fashions in cells. Therefore, there is an open space for development of the timely and relevant computational algorithms that use robust functional expression profiles towards precise classification of complex human diseases at the modular level.

resultsInspired by the insight that genes act as a module to carry out a highly integrated cellular function, we thus define a low dimension functional expression profile for data reduction. After annotating each individual gene to functional categories defined in a proper gene function classification system such as Gene Ontology applied in this study, we identify those functional categories enriched with differentially expressed genes. For each functional category or functional module, we compute a summary measure (s) for the raw expression values of the annotated genes to capture the overall activity level of the module. In this way, we can treat the gene expressions within a functional module as an integrative data point to replace the multiple values of individual genes. We compare the classification performance of decision trees based on functional expression profiles with the conventional gene expression profiles using four publicly available datasets, which indicates that precise classification of tumour types and improved interpretation can be achieved with the reduced functional expression profiles.

conclusionThis modular approach is demonstrated to be a powerful alternative approach to analyzing high dimension microarray data and is robust to high measurement noise and intrinsic biological variance inherent in microarray data. Furthermore, efficient integration with current biological knowledge has facilitated the interpretation of the underlying molecular mechanisms for complex human diseases at the modular level.

Indexed as

Gene Expression Regulation, NeoplasticAlgorithmsCluster AnalysisComputational BiologyDatabase Management SystemsDatabases, GeneticDatabases, Nucleic AcidData Interpretation, StatisticalDecision TreesGene Expression ProfilingGene Expression RegulationGenetic Predisposition to DiseaseGenomicsHumansInformation Storage and RetrievalModels, Genetic

Identifiers

PMID15774002
PMCPMC1274255

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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.