Evidence map›Paper›PMID 37430224›Full record

ArticleBMC bioinformatics2023

Supervised topological data analysis for MALDI mass spectrometry imaging applications.

Gideon Klaila, Vladimir Vutov, Anastasios Stefanou

Abstract read
In one paragraph

Article in BMC bioinformatics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
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

3 citing papers in PubMed.

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4 · The record

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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.

Gideon Klaila *Institute for Algebra, Geometry, Topology and their Applications (ALTA), University of Bremen, 28359, Bremen, Germany. klailag@uni-bremen.de.ORCID http://orcid.org/0009-0002-2861-2095
Vladimir Vutov *Institute for Statistics, University of Bremen, 28359, Bremen, Germany.ORCID http://orcid.org/0000-0002-4758-5822
Anastasios Stefanou *Institute for Algebra, Geometry, Topology and their Applications (ALTA), University of Bremen, 28359, Bremen, Germany.ORCID http://orcid.org/0000-0002-5408-9317

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMatrix-assisted laser desorption/ionization mass spectrometry imaging (MALDI MSI) displays significant potential for applications in cancer research, especially in tumor typing and subtyping. Lung cancer is the primary cause of tumor-related deaths, where the most lethal entities are adenocarcinoma (ADC) and squamous cell carcinoma (SqCC). Distinguishing between these two common subtypes is crucial for therapy decisions and successful patient management.

resultsWe propose a new algebraic topological framework, which obtains intrinsic information from MALDI data and transforms it to reflect topological persistence. Our framework offers two main advantages. Firstly, topological persistence aids in distinguishing the signal from noise. Secondly, it compresses the MALDI data, saving storage space and optimizes computational time for subsequent classification tasks. We present an algorithm that efficiently implements our topological framework, relying on a single tuning parameter. Afterwards, logistic regression and random forest classifiers are employed on the extracted persistence features, thereby accomplishing an automated tumor (sub-)typing process. To demonstrate the competitiveness of our proposed framework, we conduct experiments on a real-world MALDI dataset using cross-validation. Furthermore, we showcase the effectiveness of the single denoising parameter by evaluating its performance on synthetic MALDI images with varying levels of noise.

conclusionOur empirical experiments demonstrate that the proposed algebraic topological framework successfully captures and leverages the intrinsic spectral information from MALDI data, leading to competitive results in classifying lung cancer subtypes. Moreover, the framework's ability to be fine-tuned for denoising highlights its versatility and potential for enhancing data analysis in MALDI applications.

Indexed as

AdenocarcinomaCarcinoma, Squamous CellLung NeoplasmsData AnalysisHumansSpectrometry, Mass, Matrix-Assisted Laser Desorption-IonizationData compressionData denoisingLogistic regressionPeaks detectionPersistence transformationRandom forestTopological persistence

Identifiers

PMID37430224
PMCPMC10334630

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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.