Evidence map›Paper›PMID 40869283›Full record

ArticleInternational journal of molecular sciences2025

Feature Selection Strategies for Deep Learning-Based Classification in Ultra-High-Dimensional Genomic Data.

Krzysztof Kotlarz, Dawid Słomian, Weronika Zawadzka, Joanna Szyda

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

4 authors.

Krzysztof KotlarzBiostatistics Group, Department of Genetics, Wroclaw University of Environmental and Life Sciences, 51-631 Wroclaw, Poland.ORCID 0000-0003-2271-025X
Dawid SłomianNational Research Institute of Animal Production, 32-083 Balice, Poland.ORCID 0000-0002-9037-7703
Weronika ZawadzkaBiostatistics Group, Department of Genetics, Wroclaw University of Environmental and Life Sciences, 51-631 Wroclaw, Poland.ORCID 0009-0003-4257-0650
Joanna SzydaBiostatistics Group, Department of Genetics, Wroclaw University of Environmental and Life Sciences, 51-631 Wroclaw, Poland.ORCID 0000-0001-9688-0193

Funding

National Science Centre 2019/35/O/NZ9/00237
6 · The paper itself

Abstract

The advancement of high-throughput sequencing has revolutionised genomic research by generating large amounts of data. However, Whole-Genome Sequencing is associated with a statistical challenge known as the p >> n problem. We classified 1825 individuals into five breeds based on 11,915,233 SNPs. First, three feature selection algorithms were applied: SNP-tagging and two approaches based on supervised rank aggregation, followed by either one-dimensional (1D-SRA) or multidimensional (MD-SRA) feature clustering. Individuals were then classified into breeds using a deep learning classifier composed of Convolutional Neural Networks. SNPs selected by SNP-tagging yielded the least satisfactory F1-score (86.87%); however, this approach offered rapid computing time. The 1D-SRA was less suitable for ultra-high-dimensional data due to computational, memory, and storage limitations. However, the SNP set selected by this algorithm provided the best classification quality (96.81%). MD-SRA provided a good balance between classification quality (95.12%) and computational efficiency (17x lower analysis time, 14x lower data storage). Unlike SNP-tagging, SRA-based approaches are universal and are not limited to genomic data. This study addressed the demand for efficient computational and statistical tools for feature selection in high-dimensional genomic data. The results demonstrate that the proposed MD-SRA is suitable for the classification of high-dimensional data.

Indexed as

Deep LearningGenomicsAlgorithmsAnimalsComputational BiologyHigh-Throughput Nucleotide SequencingNeural Networks, ComputerPolymorphism, Single Nucleotidedeep learningdimensionality reductionfeature selection algorithmsmixed linear modelmulti-class classificationSNPwhole-genome sequencing

Identifiers

PMID40869283
PMCPMC12386708

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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.