Visualization Challenges of Variant Interpretation in Multiscale NGS Data
Date
2022Metadata
Show full item recordAbstract
There is currently a movement in health care towards precision medicine, where genomics often is the central diagnostic component for tailoring the treatment to the individual patient. We here present results from a domain characterization effort to pinpoint problems and possibilities for visualization of genomics data in the clinical workflow, with analysis of copy number variants as an example task. Five distinct characteristics have been identified. Clinical genomics data is inherently multiscale, riddled with artifacts and uncertainty, and many findings have unknown significance, so it is a challenging visual analytics domain. Moreover, as in other clinical domains, high efficiency is key. This characterization will form the basis for follow-on visualization prototyping.
BibTeX
@inproceedings {10.2312:evp.20221132,
booktitle = {EuroVis 2022 - Posters},
editor = {Krone, Michael and Lenti, Simone and Schmidt, Johanna},
title = {{Visualization Challenges of Variant Interpretation in Multiscale NGS Data}},
author = {Ståhlbom, Emilia and Molin, Jesper and Lundström, Claes and Ynnerman, Anders},
year = {2022},
publisher = {The Eurographics Association},
ISBN = {978-3-03868-185-4},
DOI = {10.2312/evp.20221132}
}
booktitle = {EuroVis 2022 - Posters},
editor = {Krone, Michael and Lenti, Simone and Schmidt, Johanna},
title = {{Visualization Challenges of Variant Interpretation in Multiscale NGS Data}},
author = {Ståhlbom, Emilia and Molin, Jesper and Lundström, Claes and Ynnerman, Anders},
year = {2022},
publisher = {The Eurographics Association},
ISBN = {978-3-03868-185-4},
DOI = {10.2312/evp.20221132}
}
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Except where otherwise noted, this item's license is described as Attribution 4.0 International License
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