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Visual clustering of transcriptomic data from primary and metastatic tumors — dependencies and novel pitfalls

Zitieren Sie bitte immer diese URN: urn:nbn:de:bvb:20-opus-281872
  • Personalized oncology is a rapidly evolving area and offers cancer patients therapy options that are more specific than ever. However, there is still a lack of understanding regarding transcriptomic similarities or differences of metastases and corresponding primary sites. Applying two unsupervised dimension reduction methods (t-Distributed Stochastic Neighbor Embedding (t-SNE) and Uniform Manifold Approximation and Projection (UMAP)) on three datasets of metastases (n = 682 samples) with three different data transformations (unprocessed, log10Personalized oncology is a rapidly evolving area and offers cancer patients therapy options that are more specific than ever. However, there is still a lack of understanding regarding transcriptomic similarities or differences of metastases and corresponding primary sites. Applying two unsupervised dimension reduction methods (t-Distributed Stochastic Neighbor Embedding (t-SNE) and Uniform Manifold Approximation and Projection (UMAP)) on three datasets of metastases (n = 682 samples) with three different data transformations (unprocessed, log10 as well as log10 + 1 transformed values), we visualized potential underlying clusters. Additionally, we analyzed two datasets (n = 616 samples) containing metastases and primary tumors of one entity, to point out potential familiarities. Using these methods, no tight link between the site of resection and cluster formation outcome could be demonstrated, or for datasets consisting of solely metastasis or mixed datasets. Instead, dimension reduction methods and data transformation significantly impacted visual clustering results. Our findings strongly suggest data transformation to be considered as another key element in the interpretation of visual clustering approaches along with initialization and different parameters. Furthermore, the results highlight the need for a more thorough examination of parameters used in the analysis of clusters.zeige mehrzeige weniger

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Autor(en): André Marquardt, Philip Kollmannsberger, Markus Krebs, Antonella Argentiero, Markus Knott, Antonio Giovanni Solimando, Alexander Georg Kerscher
URN:urn:nbn:de:bvb:20-opus-281872
Dokumentart:Artikel / Aufsatz in einer Zeitschrift
Institute der Universität:Medizinische Fakultät / Urologische Klinik und Poliklinik
Medizinische Fakultät / Pathologisches Institut
Fakultät für Biologie / Center for Computational and Theoretical Biology
Medizinische Fakultät / Comprehensive Cancer Center Mainfranken
Sprache der Veröffentlichung:Englisch
Titel des übergeordneten Werkes / der Zeitschrift (Englisch):Genes
ISSN:2073-4425
Erscheinungsjahr:2022
Band / Jahrgang:13
Heft / Ausgabe:8
Aufsatznummer:1335
Originalveröffentlichung / Quelle:Genes (2022) 13:8, 1335. doi:10.3390/genes13081335
DOI:https://doi.org/10.3390/genes13081335
Allgemeine fachliche Zuordnung (DDC-Klassifikation):6 Technik, Medizin, angewandte Wissenschaften / 61 Medizin und Gesundheit / 610 Medizin und Gesundheit
Freie Schlagwort(e):UMAP; cancer; metastasis; t-SNE; transcriptomic analysis; visual clustering
Datum der Freischaltung:20.04.2023
Datum der Erstveröffentlichung:26.07.2022
Open-Access-Publikationsfonds / Förderzeitraum 2022
Lizenz (Deutsch):License LogoCC BY: Creative-Commons-Lizenz: Namensnennung 4.0 International