Evidence map›Paper›PMID 29247873›Full record

ArticleGenomics, proteomics & bioinformatics2017

The Ability of Different Imputation Methods to Preserve the Significant Genes and Pathways in Cancer.

Rosa Aghdam, Taban Baghfalaki, Pegah Khosravi, Elnaz Saberi Ansari

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Article in Genomics, proteomics & bioinformatics, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

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0cells of the map it votes in
4citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Rosa AghdamSchool of Biological Science, Institute for Research in Fundamental Sciences (IPM), Tehran 19395-5746, Iran. Electronic address: rosaaghdam@ipm.ir.
Taban BaghfalakiDepartment of Statistics, Faculty of Mathematical Sciences, Tarbiat Modares University, Tehran 14115-111, Iran.
Pegah KhosraviSchool of Biological Science, Institute for Research in Fundamental Sciences (IPM), Tehran 19395-5746, Iran; Department of Physiology and Biophysics, Institute for Computational Biomedicine and Institute for Precision Medicine, Weill Cornell Medical College, New York, NY 10021, USA.
Elnaz Saberi AnsariSchool of Biological Science, Institute for Research in Fundamental Sciences (IPM), Tehran 19395-5746, Iran; Institut Cochin, Inserm U1016, CNRS UMR 8104, Universit Paris Descartes UMR-S1016, F-75014 Paris, France. Electronic address: elnaz.saberiansari@ipm.ir.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Deciphering important genes and pathways from incomplete gene expression data could facilitate a better understanding of cancer. Different imputation methods can be applied to estimate the missing values. In our study, we evaluated various imputation methods for their performance in preserving significant genes and pathways. In the first step, 5% genes are considered in random for two types of ignorable and non-ignorable missingness mechanisms with various missing rates. Next, 10 well-known imputation methods were applied to the complete datasets. The significance analysis of microarrays (SAM) method was applied to detect the significant genes in rectal and lung cancers to showcase the utility of imputation approaches in preserving significant genes. To determine the impact of different imputation methods on the identification of important genes, the chi-squared test was used to compare the proportions of overlaps between significant genes detected from original data and those detected from the imputed datasets. Additionally, the significant genes are tested for their enrichment in important pathways, using the ConsensusPathDB. Our results showed that almost all the significant genes and pathways of the original dataset can be detected in all imputed datasets, indicating that there is no significant difference in the performance of various imputation methods tested. The source code and selected datasets are available on http://profiles.bs.ipm.ir/softwares/imputation_methods/.

Indexed as

AlgorithmsComputational BiologyDatabases, GeneticGenes, NeoplasmHumansNeoplasmsReplication Protein CSignal TransductionReplication Protein CRFC2 protein, humanGene expressionImputation methodMissing dataPathway enrichmentSignificant genes

Identifiers

PMID29247873
PMCPMC5828654

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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.