Data

16.4T MRI of nephrectomy sample - updated

The University of Queensland
Dr Nyoman Kurniawan (Aggregated by) Dr Nyoman Kurniawan (Aggregated by)
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ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Adc&rfr_id=info%3Asid%2FANDS&rft_id=info:doi10.48610/7da7765&rft.title=16.4T MRI of nephrectomy sample - updated&rft.identifier=RDM ID: 10ca5e49-279f-4df6-9ca2-94df008e1e84&rft.publisher=The University of Queensland&rft.description=Tissue samples were obtained from whole kidney post-nephrectomy without flushing the blood, fixed in formalin for 24 h and washed with saline for 3 d at 4°C prior to scanning. Samples were scanned at room temperature using a Bruker Biospec 16.4 T MRI at the Centre for Advanced Imaging, The University of Queensland. This scanner is equipped with a Micro2.5 gradient (1.5 T/m at 60 A). Microimaging coils appropriate to the size of the samples were used, these included a 15×30 mm surface coil, a 15 mm and a 10 mm volume coil. Samples were either placed in saline or wrapped with paraffin film to minimise air artefacts. MRI was performed using a 3D T1/T2*-weighted gradient echo (GRE) sequence with repetition time TR = 150 ms, echo time TE = 6.2 ms, flip angle 60°. Typically, the field-of-view was ~2.4×1.2×1.2 cm with the matrix sizes set to produce images at 30 μm 3D isotropic resolutions. The acquisition times were approximately 27 h (number of excitations (NEX) = 4). A sine windowing function was applied to the K-space data prior to the Fourier transform to reduce the noise in the 30 μm images.&rft.creator=Dr Nyoman Kurniawan&rft.creator=Dr Nyoman Kurniawan&rft.date=2025&rft_rights= https://guides.library.uq.edu.au/deposit-your-data/license-reuse-data-agreement&rft_subject=eng&rft_subject=Nephrology and urology&rft_subject=Clinical sciences&rft_subject=BIOMEDICAL AND CLINICAL SCIENCES&rft_subject=Biomedical imaging&rft_subject=Biomedical engineering&rft_subject=ENGINEERING&rft_subject=Image processing&rft_subject=Computer vision and multimedia computation&rft_subject=INFORMATION AND COMPUTING SCIENCES&rft.type=dataset&rft.language=English Access the data

Contact Information

nyoman.kurniawan@cai.uq.edu.au
Australian Institute for Bioengineering and Nanotechnology

Full description

Tissue samples were obtained from whole kidney post-nephrectomy without flushing the blood, fixed in formalin for 24 h and washed with saline for 3 d at 4°C prior to scanning. Samples were scanned at room temperature using a Bruker Biospec 16.4 T MRI at the Centre for Advanced Imaging, The University of Queensland. This scanner is equipped with a Micro2.5 gradient (1.5 T/m at 60 A). Microimaging coils appropriate to the size of the samples were used, these included a 15×30 mm surface coil, a 15 mm and a 10 mm volume coil. Samples were either placed in saline or wrapped with paraffin film to minimise air artefacts. MRI was performed using a 3D T1/T2*-weighted gradient echo (GRE) sequence with repetition time TR = 150 ms, echo time TE = 6.2 ms, flip angle 60°. Typically, the field-of-view was ~2.4×1.2×1.2 cm with the matrix sizes set to produce images at 30 μm 3D isotropic resolutions. The acquisition times were approximately 27 h (number of excitations (NEX) = 4). A sine windowing function was applied to the K-space data prior to the Fourier transform to reduce the noise in the 30 μm images.

Issued: 2025

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local : UQ:289097

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