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Phot-IQA: A photoacoustic image data set with image quality ratings

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Abstract

Image quality assessment (IQA) is crucial in the evaluation stage of novel algorithms operating on images, including traditional and machine learning based methods. Due to the lack of available quality-rated medical images, most commonly used full-reference IQA measures have been developed and tested for natural images. Reported pitfalls and inconsistencies arising when applying such measures for medical images are not surprising, as they rely on different properties than natural images. In photoacoustic imaging (PAI), especially, standard benchmarking approaches for assessing the quality of image reconstructions are lacking. PAI is a multi-physics imaging modality, in which two inverse problems have to be solved, which makes the application of IQA measures uniquely challenging due to both, acoustic and optical, artifacts. To support the development and testing of IQA measures we assembled PhotIQA, a data set consisting of 1134 photoacoustic images. The images were rated by five experts across five quality properties in a full-reference setting, where the detailed rating enables usage beyond PAI. The data set with the images and corresponding ratings is publicly available on Zenodo.

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2052-4463
2052-4463

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Nature Portfolio

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Except where otherwised noted, this item's license is described as Attribution 4.0 International
Sponsorship
The authors wish to acknowledge support from the EU/EFPIA Innovative Medicines Initiative 2 Joint Undertaking - DRAGON (101005122) (A.Br., I.S., C.B.S.); the Austrian Science Fund (FWF) through project T1307 (A.Br., C.K.); the German Research Foundation through the grant GR 5824/1 (J.G.) and project number 462569370 (T.R.); EPSRC UK EP/X037770/1 (T.R.E.); Cancer Research UK through C9545/A29580 (T.R.E); the ERC under the European Union’s Horizon research and innovation programme through project NEURAL SPICING (grant 101002198) (T.R.),the NIHR Cambridge Biomedical Research Centre (BRC-1215-20014) (I.S.) and (NIHR203312) (C.B.S); C.B.S also acknowledges support from the Philip Leverhulme Prize, the Royal Society Wolfson Fellowship, the EPSRC (EP/V029428/1, EP/V026259/1, EP/S026045/1, EP/T003553/1, EP/N014588/1, EP/T017961/1, the Wellcome Innovator Awards 215733/Z/19/Z and 221633/Z/20/Z, the EPSRC funded ProbAI hub EP/Y028783/1), and the European Union Horizon 2020 research and innovation programme under the Marie Skodowska-Curie grant agreement REMODEL.