Data

Extracellular vesicle-based miR-122-5p correlates with liver fat and liver enzymes in metabolic dysfunction-associated steatotic liver disease.

The University of Queensland
Dr Dominic Guanzon (Aggregated by) Dr Dominic Guanzon (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/aaba5e5&rft.title=Extracellular vesicle-based miR-122-5p correlates with liver fat and liver enzymes in metabolic dysfunction-associated steatotic liver disease.&rft.identifier=RDM ID: 89c028f6-03c5-44bf-bdf7-5cc3ecde7ebd&rft.publisher=The University of Queensland&rft.description=This dataset contains FASTQ files, raw microRNA count data, and sample information from patients participating in the MULTISITE study, a longitudinal intervention study investigating the effects of a personalised weight-loss intervention on metabolic dysfunction-associated steatotic liver disease (MASLD). Extracellular vesicles (EVs) were isolated from plasma using the Mag-Net method. RNA was extracted using the Norgen Biotek Exosomal RNA Extraction Kit and used to generate small RNA libraries with the NEXTFLEX® Small RNA-seq v4 Kit with UDIs. The protocol was modified to incorporate gel-based size selection instead of bead-based size selection, consistent with the approach used in the earlier NEXTFLEX® Small RNA-seq v3 Kit. Libraries were quantified using the KAPA Library Quantification Kit and pooled in equimolar concentrations. The pooled library was sequenced on a NextSeq 500 using a High Output 75-cycle kit, generating single-index (8 bp) reads and 76 bp single-end reads.&rft.creator=Dr Dominic Guanzon&rft.creator=Dr Dominic Guanzon&rft.date=2026&rft_rights= http://guides.library.uq.edu.au/deposit_your_data/terms_and_conditions&rft_subject=eng&rft_subject=Bioinformatics and computational biology&rft_subject=BIOLOGICAL SCIENCES&rft_subject=BIOMEDICAL AND CLINICAL SCIENCES&rft.type=dataset&rft.language=English Access the data

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UQ Centre for Clinical Research

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This dataset contains FASTQ files, raw microRNA count data, and sample information from patients participating in the MULTISITE study, a longitudinal intervention study investigating the effects of a personalised weight-loss intervention on metabolic dysfunction-associated steatotic liver disease (MASLD). Extracellular vesicles (EVs) were isolated from plasma using the Mag-Net method. RNA was extracted using the Norgen Biotek Exosomal RNA Extraction Kit and used to generate small RNA libraries with the NEXTFLEX® Small RNA-seq v4 Kit with UDIs. The protocol was modified to incorporate gel-based size selection instead of bead-based size selection, consistent with the approach used in the earlier NEXTFLEX® Small RNA-seq v3 Kit. Libraries were quantified using the KAPA Library Quantification Kit and pooled in equimolar concentrations. The pooled library was sequenced on a NextSeq 500 using a High Output 75-cycle kit, generating single-index (8 bp) reads and 76 bp single-end reads.

Issued: 05 03 2026

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