Evidence map›Paper›PMID 35596135›Full record

ArticleBMC bioinformatics2022

Gene expression data classification using topology and machine learning models.

Tamal K Dey, Sayan Mandal, Soham Mukherjee

Abstract read
In one paragraph

Article in BMC bioinformatics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

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

2 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

3 authors.

Tamal K DeyDepartment of Computer Science, Purdue University, West Lafayette, IN, USA.
Sayan MandalDepartment of Computer Science and Engineering, The Ohio State University, Columbus, OH, USA.
Soham MukherjeeDepartment of Computer Science, Purdue University, West Lafayette, IN, USA. mukher26@purdue.edu.ORCID http://orcid.org/0000-0003-0486-7763

Funding

National Science Foundation ccf-1839252National Science Foundation ccf-2049010
6 · The paper itself

Abstract

backgroundInterpretation of high-throughput gene expression data continues to require mathematical tools in data analysis that recognizes the shape of the data in high dimensions. Topological data analysis (TDA) has recently been successful in extracting robust features in several applications dealing with high dimensional constructs. In this work, we utilize some recent developments in TDA to curate gene expression data. Our work differs from the predecessors in two aspects: (1) Traditional TDA pipelines use topological signatures called barcodes to enhance feature vectors which are used for classification. In contrast, this work involves curating relevant features to obtain somewhat better representatives with the help of TDA. This representatives of the entire data facilitates better comprehension of the phenotype labels. (2) Most of the earlier works employ barcodes obtained using topological summaries as fingerprints for the data. Even though they are stable signatures, there exists no direct mapping between the data and said barcodes.

resultsThe topology relevant curated data that we obtain provides an improvement in shallow learning as well as deep learning based supervised classifications. We further show that the representative cycles we compute have an unsupervised inclination towards phenotype labels. This work thus shows that topological signatures are able to comprehend gene expression levels and classify cohorts accordingly.

conclusionsIn this work, we engender representative persistent cycles to discern the gene expression data. These cycles allow us to directly procure genes entailed in similar processes.

Indexed as

Data AnalysisMachine LearningGene ExpressionGene expressionNeural networkPersistent cyclesTopological data analysis

Identifiers

PMID35596135
PMCPMC9121583

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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.