Evidence map›Paper›PMID 38429657›Full record

ArticleBMC bioinformatics2024

Few-shot genes selection: subset of PAM50 genes for breast cancer subtypes classification.

Leandro Y S Okimoto, Rayol Mendonca-Neto, Fabíola G Nakamura, Eduardo F Nakamura, David Fenyö, Claudio T Silva

Abstract read
In one paragraph

Article in BMC bioinformatics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 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

6 authors.

Leandro Y S OkimotoInstitute of Computing, Universidade Federal do Amazonas, Manaus, BR, Brazil. okimoto@icomp.ufam.edu.br.
Rayol Mendonca-NetoInstitute of Computing, Universidade Federal do Amazonas, Manaus, BR, Brazil.
Fabíola G NakamuraInstitute of Computing, Universidade Federal do Amazonas, Manaus, BR, Brazil.
Eduardo F NakamuraInstitute of Computing, Universidade Federal do Amazonas, Manaus, BR, Brazil.
David FenyöNew York Univesity, New York, USA.
Claudio T SilvaNew York Univesity, New York, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIn recent years, researchers have made significant strides in understanding the heterogeneity of breast cancer and its various subtypes. However, the wealth of genomic and proteomic data available today necessitates efficient frameworks, instruments, and computational tools for meaningful analysis. Despite its success as a prognostic tool, the PAM50 gene signature's reliance on many genes presents challenges in terms of cost and complexity. Consequently, there is a need for more efficient methods to classify breast cancer subtypes using a reduced gene set accurately.

resultsThis study explores the potential of achieving precise breast cancer subtype categorization using a reduced gene set derived from the PAM50 gene signature. By employing a "Few-Shot Genes Selection" method, we randomly select smaller subsets from PAM50 and evaluate their performance using metrics and a linear model, specifically the Support Vector Machine (SVM) classifier. In addition, we aim to assess whether a more compact gene set can maintain performance while simplifying the classification process. Our findings demonstrate that certain reduced gene subsets can perform comparable or superior to the full PAM50 gene signature.

conclusionsThe identified gene subsets, with 36 genes, have the potential to contribute to the development of more cost-effective and streamlined diagnostic tools in breast cancer research and clinical settings.

Indexed as

Breast NeoplasmsBiomarkers, TumorFemaleGene Expression ProfilingGenetic TechniquesHumansProteomicsBiomarkers, TumorBreast cancer subtypesEXplainable AIGene expressionPAM50

Identifiers

PMID38429657
PMCPMC10908178

What Socratic holds

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Registered trials

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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 Socratic graph.