Evidence map›Paper›PMID 16509965›Full record

ArticleBMC bioinformatics2006

A multivariate prediction model for microarray cross-hybridization.

Yian A Chen, Cheng-Chung Chou, Xinghua Lu, Elizabeth H Slate, Konan Peck, Wenying Xu, Eberhard O Voit, Jonas S Almeida

Abstract read
In one paragraph

Article in BMC bioinformatics, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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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

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3 · Its place in the literature

Who cites it

15 citing papers in PubMed.

  1. Article
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  4. Article
  5. Compressive sensing DNA microarrays.EURASIP journal on bioinformatics & systems biology · 2009
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  8. Review
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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

8 authors.

Yian A ChenDepartment of Biostatistics, Bioinformatics, and Epidemiology, Medical University of South Carolina, Charleston, SC, USA. chenya@musc.edu
Cheng-Chung Chou
Xinghua Lu
Elizabeth H Slate
Konan Peck
Wenying Xu
Eberhard O Voit
Jonas S Almeida

Funding

NHLBI PROTEOMICS INITIATIVE-N01HV28181N01HV028181 · HV · MEDICAL UNIV OF SOUTH CAROLINA · PI KNAPP, DANIEL · 2002 to 2006
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NHLBI NIH HHS N01-HV-281-81-000
6 · The paper itself

Abstract

backgroundExpression microarray analysis is one of the most popular molecular diagnostic techniques in the post-genomic era. However, this technique faces the fundamental problem of potential cross-hybridization. This is a pervasive problem for both oligonucleotide and cDNA microarrays; it is considered particularly problematic for the latter. No comprehensive multivariate predictive modeling has been performed to understand how multiple variables contribute to (cross-) hybridization.

resultsWe propose a systematic search strategy using multiple multivariate models [multiple linear regressions, regression trees, and artificial neural network analyses (ANNs)] to select an effective set of predictors for hybridization. We validate this approach on a set of DNA microarrays with cytochrome p450 family genes. The performance of our multiple multivariate models is compared with that of a recently proposed third-order polynomial regression method that uses percent identity as the sole predictor. All multivariate models agree that the 'most contiguous base pairs between probe and target sequences,' rather than percent identity, is the best univariate predictor. The predictive power is improved by inclusion of additional nonlinear effects, in particular target GC content, when regression trees or ANNs are used.

conclusionA systematic multivariate approach is provided to assess the importance of multiple sequence features for hybridization and of relationships among these features. This approach can easily be applied to larger datasets. This will allow future developments of generalized hybridization models that will be able to correct for false-positive cross-hybridization signals in expression experiments.

Indexed as

AlgorithmsModels, GeneticArtifactsComputer SimulationIn Situ HybridizationModels, StatisticalMultivariate AnalysisOligonucleotide Array Sequence AnalysisSequence Analysis, DNA

Identifiers

PMID16509965
PMCPMC1409802

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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.