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Deciphering cancer genomes with GenomeSpy : a grammar-based visualization toolkit

Lavikka, Kari; Oikkonen, Jaana; Li, Yilin; Muranen, Taru; Micoli, Giulia; Marchi, Giovanni; Lahtinen, Alexandra; Huhtinen, Kaisa; Lehtonen, Rainer; Hietanen, Sakari; Hynninen, Johanna; Virtanen, Anni; Hautaniemi, Sampsa

Deciphering cancer genomes with GenomeSpy : a grammar-based visualization toolkit

Lavikka, Kari
Oikkonen, Jaana
Li, Yilin
Muranen, Taru
Micoli, Giulia
Marchi, Giovanni
Lahtinen, Alexandra
Huhtinen, Kaisa
Lehtonen, Rainer
Hietanen, Sakari
Hynninen, Johanna
Virtanen, Anni
Hautaniemi, Sampsa
Katso/Avaa
giae040.pdf (2.801Mb)
Lataukset: 

Oxford University Press
doi:10.1093/gigascience/giae040
URI
https://academic.oup.com/gigascience/article/doi/10.1093/gigascience/giae040/7727441
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Julkaisun pysyvä osoite on:
https://urn.fi/URN:NBN:fi-fe2025082784918
Tiivistelmä

Background: Visualization is an indispensable facet of genomic data analysis. Despite the abundance of specialized visualization tools, there remains a distinct need for tailored solutions. However, their implementation typically requires extensive programming expertise from bioinformaticians and software developers, especially when building interactive applications. Toolkits based on visualization grammars offer a more accessible, declarative way to author new visualizations. Yet, current grammar-based solutions fall short in adequately supporting the interactive analysis of large datasets with extensive sample collections, a pivotal task often encountered in cancer research.

Findings: We present GenomeSpy, a grammar-based toolkit for authoring tailored, interactive visualizations for genomic data analysis. By using combinatorial building blocks and a declarative language, users can implement new visualization designs easily and embed them in web pages or end-user-oriented applications. A distinctive element of GenomeSpy's architecture is its effective use of the graphics processing unit in all rendering, enabling a high frame rate and smoothly animated interactions, such as navigation within a genome. We demonstrate the utility of GenomeSpy by characterizing the genomic landscape of 753 ovarian cancer samples from patients in the DECIDER clinical trial. Our results expand the understanding of the genomic architecture in ovarian cancer, particularly the diversity of chromosomal instability.

Conclusions: GenomeSpy is a visualization toolkit applicable to a wide range of tasks pertinent to genome analysis. It offers high flexibility and exceptional performance in interactive analysis. The toolkit is open source with an MIT license, implemented in JavaScript, and available at https://genomespy.app/.

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