Evidence map›Paper›PMID 41479073›Full record

ArticleAdvances in experimental medicine and biology2026

Comparative Analysis of High-Throughput Data in AML Detection.

Anastasios Theodorou, Costas Papaloukas

Abstract readComparative Study
PubMed Publisher
In one paragraph

Article in Advances in experimental medicine and biology, 2026. 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

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

2 authors.

Anastasios TheodorouDepartment of Biological Applications and Technologies, University of Ioannina, Ioannina, Greece.
Costas PapaloukasDepartment of Biological Applications and Technologies, University of Ioannina, Ioannina, Greece. papalouk@uoi.gr.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Acute myeloid leukemia (AML) is a heterogeneous hematological melanoma disease, which faces significant challenges in diagnosis and treatment due to its genetic complexity and variable clinical outcomes.NF342 by juxtaposition with MPO promoter/enhan In the current work, the potential of microarrays and next-generation RNA sequencing (RNA-seq) is assessed for the study of cancer and specifically to separate differences in expression that distinguish samples with AML from control ones. By using datasets derived from microarrays and RNA-seq, the study observes that there are differences in gene expression between AML samples and control. The selected probes were used as a foundation in the development of a classifier that can distinguish the AML samples. The probes then underwent cross-mapping from the microarrays platform to the RNA-seq one and vice versa. This ensured the adaptability and the reliability of the classifier on different platforms. The classifier that was trained (using probes from the same platform) showed greater reliability in the dataset from next-generation RNA-seq platform, with an accuracy of 98.9%, 98.7% sensitivity, and 100% specificity. However, when opposite platform probes were used, that underwent cross-mapping, the reliability of the classifier in the dataset from microarrays platform significantly increased. In particular, it reached an accuracy of 99.3%, 99.4% specificity, and a sensitivity of 96.4%. Lastly, the selection methods were used again with a higher number of genes and then gene set enrichment analysis was performed to find the pathways where the genes are connected. This showed the significance of multiple pathways including "Protein processing in endoplasmic reticulum Homo sapiens hsa04141" and "Proteoglycans in cancer Homo sapiens hsa05205."

Indexed as

Biomarkers, TumorHigh-Throughput Nucleotide SequencingLeukemia, Myeloid, AcuteGene Expression ProfilingGene Expression Regulation, LeukemicHumansOligonucleotide Array Sequence AnalysisReproducibility of ResultsRNA-SeqBiomarkers, TumorAcute Myeloid LeukemiaGene Set Enrichment AnalysisLogistic Regression ClassifierMicroarraysRNA-sequencing

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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.