Evidence map›Paper›PMID 24361387›Full record

ArticleJournal of biomedical informatics2014

A novel artificial neural network method for biomedical prediction based on matrix pseudo-inversion.

Binghuang Cai, Xia Jiang

Abstract read
In one paragraph

Article in Journal of biomedical informatics, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 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

2 authors.

Binghuang CaiDepartment of Biomedical Informatics, School of Medicine, University of Pittsburgh, Pittsburgh, PA 15206-3701, USA. Electronic address: bic9@pitt.edu.
Xia JiangDepartment of Biomedical Informatics, School of Medicine, University of Pittsburgh, Pittsburgh, PA 15206-3701, USA. Electronic address: xij6@pitt.edu.

Funding

Detecting Genome Wide Epistasis with Efficient Bayesian Network LearningR00LM010822 · NLM · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI JIANG, XIA · 2012 to 2014
$565k
Detecting Genome Wide Epistasis with Efficient Bayesian Network LearningK99LM010822 · NLM · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI JIANG, XIA · 2010 to 2011
$180k
NLM NIH HHS K99 LM010822NLM NIH HHS LM010822NLM NIH HHS R00 LM010822
6 · The paper itself

Abstract

Biomedical prediction based on clinical and genome-wide data has become increasingly important in disease diagnosis and classification. To solve the prediction problem in an effective manner for the improvement of clinical care, we develop a novel Artificial Neural Network (ANN) method based on Matrix Pseudo-Inversion (MPI) for use in biomedical applications. The MPI-ANN is constructed as a three-layer (i.e., input, hidden, and output layers) feed-forward neural network, and the weights connecting the hidden and output layers are directly determined based on MPI without a lengthy learning iteration. The LASSO (Least Absolute Shrinkage and Selection Operator) method is also presented for comparative purposes. Single Nucleotide Polymorphism (SNP) simulated data and real breast cancer data are employed to validate the performance of the MPI-ANN method via 5-fold cross validation. Experimental results demonstrate the efficacy of the developed MPI-ANN for disease classification and prediction, in view of the significantly superior accuracy (i.e., the rate of correct predictions), as compared with LASSO. The results based on the real breast cancer data also show that the MPI-ANN has better performance than other machine learning methods (including support vector machine (SVM), logistic regression (LR), and an iterative ANN). In addition, experiments demonstrate that our MPI-ANN could be used for bio-marker selection as well.

Indexed as

Neural Networks, ComputerSupport Vector MachineAlgorithmsArtificial IntelligenceBreast NeoplasmsFemaleGenomicsHumansMedical InformaticsModels, StatisticalNeoplasmsPolymorphism, Single NucleotideRegression AnalysisReproducibility of ResultsBiomedical prediction and classificationCancerLeast Absolute Shrinkage and Selection Operator (LASSO)Matrix pseudo-inversionNeural networksSingle Nucleotide Polymorphism (SNP)

Identifiers

PMID24361387
PMCPMC4004678

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.