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<p>Dense longitudinal neuroimaging usually requires substantial institutional resources, yet can also be achieved by an individual using standard clinical MRI infrastructure. This work presents a multimodal single-subject dataset comprising 85 hours of resting-state fMRI acquired over 11 months, including 51.6 hours under a standardized protocol (paired eyes-open/-closed runs, 128 sessions over 7.5 months). Additional data include 195 T1-weighted structural scans, 54 diffusion MRI sessions, physiological recordings, pre-session behavioral assessments, and detailed medication and lifestyle logs. Scans were collected primarily via self-administered acquisition on a clinical 3 T system, with sub-3 mm between-session positioning reproducibility observed in later sessions. Quality control identified 58 hours of low-motion data (mean framewise displacement &lt;0.2 mm), with higher-motion runs occurring predominantly during sleep. The acquisition period included antidepressant dose changes and seasonal variation, forming a single-subject naturalistic context with collinear factors that preclude causal inference. The dataset follows the BIDS standard and is intended for methodological development, reliability analyses, preprocessing benchmarking, and educational use.</p>

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A dense longitudinal multimodal single-subject rs-fMRI dataset acquired by self-administered scanning

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  • 出版模式：

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  • 发表日期：

    2026年2月21日

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  • Evgeny D. Petrovskiy

摘要

Dense longitudinal neuroimaging usually requires substantial institutional resources, yet can also be achieved by an individual using standard clinical MRI infrastructure. This work presents a multimodal single-subject dataset comprising 85 hours of resting-state fMRI acquired over 11 months, including 51.6 hours under a standardized protocol (paired eyes-open/-closed runs, 128 sessions over 7.5 months). Additional data include 195 T1-weighted structural scans, 54 diffusion MRI sessions, physiological recordings, pre-session behavioral assessments, and detailed medication and lifestyle logs. Scans were collected primarily via self-administered acquisition on a clinical 3 T system, with sub-3 mm between-session positioning reproducibility observed in later sessions. Quality control identified 58 hours of low-motion data (mean framewise displacement <0.2 mm), with higher-motion runs occurring predominantly during sleep. The acquisition period included antidepressant dose changes and seasonal variation, forming a single-subject naturalistic context with collinear factors that preclude causal inference. The dataset follows the BIDS standard and is intended for methodological development, reliability analyses, preprocessing benchmarking, and educational use.