Open-Source Implementation for X-Nuclear and Multi-Site Sequences within the Pulseq Framework

Motivation: Support X-nuclear and vendor-neutral acquisitions for sharing and scanning across scanners and sites. Goal(s): Build a GE interpreter for X-nuclear acquisition using Pulseq framework; create a modular sequence that can support fast and flexible X-nuclear acquisition. Approach: X-nuclei capabilities were built into TOPPE GE interpreter. A modular 2D GRE spiral sequence was developed, integrating a flexible RF and readout module, and evaluated by both phantom and in-vivo studies. Results: Data from 31P, 2H, and 13C phantoms, multi-site 13C phantom, 2H-MRS brain volunteer, and hyperpolarized [1-13C]pyruvate animal studies demonstrated the feasibility, flexibility and reproducibility of the TOPPE MNS GE interpreter and modular spiral sequence. Impact: X-nuclear sequence developers can now more easily transfer their sequences across vendors and software for multi-site studies.

Authors

Publication Details

Journal
Proceedings on CD-ROM - International Society for Magnetic Resonance in Medicine. Scientific Meeting and Exhibition/Proceedings of the International Society for Magnetic Resonance in Medicine, Scientific Meeting and Exhibition
Published
2025-09-16
DOI
https://doi.org/10.58530/2025/1273
Primary Topic
Particle physics theoretical and experimental studies
Type
article
Field-Weighted Citation Impact
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article

Open-Source Implementation for X-Nuclear and Multi-Site Sequences within the Pulseq Framework

Zhen Wang, Jon‐Fredrik Nielsen, Robert Schulte, Duan Xu et al.
Proceedings on CD-ROM - International Society for Magnetic Resonance in Medicine. Scientific Meeting and Exhibition/Proceedings of the International Society for Magnetic Resonance in Medicine, Scientific Meeting and Exhibition
Particle physics theoretical and experimental studies
article

Open-Source Implementation for X-Nuclear and Multi-Site Sequences within the Pulseq Framework

Zhen Wang, Jon‐Fredrik Nielsen, Robert Schulte, Duan Xu, Daniel B. Vigneron, Peder E. Z. Larson, Jeremy W. Gordon, Dirk Mayer, Andreas Korzowski, Robert R. Flavell, Changhua Mu, Xiaoxi Liu, Di Cui, Lucas Carvajal
article en

Abstract

Motivation: Support X-nuclear and vendor-neutral acquisitions for sharing and scanning across scanners and sites. Goal(s): Build a GE interpreter for X-nuclear acquisition using Pulseq framework; create a modular sequence that can support fast and flexible X-nuclear acquisition. Approach: X-nuclei capabilities were built into TOPPE GE interpreter. A modular 2D GRE spiral sequence was developed, integrating a flexible RF and readout module, and evaluated by both phantom and in-vivo studies. Results: Data from 31P, 2H, and 13C phantoms, multi-site 13C phantom, 2H-MRS brain volunteer, and hyperpolarized [1-13C]pyruvate animal studies demonstrated the feasibility, flexibility and reproducibility of the TOPPE MNS GE interpreter and modular spiral sequence. Impact: X-nuclear sequence developers can now more easily transfer their sequences across vendors and software for multi-site studies.

Proceedings on CD-ROM - International Society for Magnetic Resonance in Medicine. Scientific Meeting and Exhibition/Proceedings of the International Society for Magnetic Resonance in Medicine, Scientific Meeting and Exhibition
Openalex Percentile: Top 90%
Particle physics theoretical and experimental studies
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Open-Source Implementation for X-Nuclear and Multi-Site Sequences within the Pulseq Framework — Zhen Wang, Jon‐Fredrik Nielsen, et al. · Proceedings on CD-ROM - International Society for Magnetic Resonance in Medicine. Scientific Meeting and Exhibition/Proceedings of the International Society for Magnetic Resonance in Medicine, Scientific Meeting and Exhibition (2025) | TGRS Research Map | TGRS