Evidence map›Paper›PMID 18554411›Full record

ArticleBMC bioinformatics2008

Using the information embedded in the testing sample to break the limits caused by the small sample size in microarray-based classification.

Manli Zhu, Aleix M Martinez

Abstract read
In one paragraph

Article in BMC bioinformatics, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

2 authors.

Manli ZhuDepartment of Electrical and Computer Engineering, The Ohio State University, Columbus, OH 43210, USA. zhum.osu@gmail.com
Aleix M Martinez

Funding

Modeling the Nonmanuals in American Sign LanguageR01DC005241 · NIDCD · PURDUE UNIVERSITY WEST LAFAYETTE · PI WILBUR, RONNIE B · 2004 to 2008
$2.4M
NIDCD NIH HHS R01 DC 005241NIDCD NIH HHS R01 DC005241
6 · The paper itself

Abstract

backgroundMicroarray-based tumor classification is characterized by a very large number of features (genes) and small number of samples. In such cases, statistical techniques cannot determine which genes are correlated to each tumor type. A popular solution is the use of a subset of pre-specified genes. However, molecular variations are generally correlated to a large number of genes. A gene that is not correlated to some disease may, by combination with other genes, express itself.

resultsIn this paper, we propose a new classiification strategy that can reduce the effect of over-fitting without the need to pre-select a small subset of genes. Our solution works by taking advantage of the information embedded in the testing samples. We note that a well-defined classification algorithm works best when the data is properly labeled. Hence, our classification algorithm will discriminate all samples best when the testing sample is assumed to belong to the correct class. We compare our solution with several well-known alternatives for tumor classification on a variety of publicly available data-sets. Our approach consistently leads to better classification results.

conclusionStudies indicate that thousands of samples may be required to extract useful statistical information from microarray data. Herein, it is shown that this problem can be circumvented by using the information embedded in the testing samples.

Indexed as

Gene Expression ProfilingAlgorithmsGene Expression Regulation, NeoplasticHumansNeoplasmsOligonucleotide Array Sequence Analysis

Identifiers

PMID18554411
PMCPMC2443146

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Registered trials

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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.