# Algebraic methods and computational strategies for pseudoinverse-based MR image reconstruction (Pinv-Recon)

**Authors:** Kylie Yeung, Christine Tobler, Rolf F. Schulte, Benjamin White, Anthony McIntyre, Sébastien Serres, Peter Morris, Dorothee Auer, Fergus V. Gleeson, Damian J. Tyler, James T. Grist, Florian Wiesinger

PMC · DOI: 10.1038/s41598-025-21929-z · 2025-10-30

## TL;DR

This paper revisits pseudoinverse-based MRI reconstruction, showing it is now computationally efficient and versatile for various imaging tasks.

## Contribution

The study demonstrates a two-order-of-magnitude improvement in computational efficiency using Cholesky decomposition for Pinv-Recon.

## Key findings

- Cholesky decomposition improves Pinv-Recon efficiency by two orders of magnitude compared to SVD-based methods.
- Pinv-Recon is versatile for diverse in vivo datasets, including low- to high-resolution imaging.
- Modern hardware and optimized routines make Pinv-Recon computationally feasible and robust.

## Abstract

Image reconstruction in Magnetic Resonance Imaging (MRI) is fundamentally a linear inverse problem, such that the image can be recovered via explicit pseudoinversion of the encoding matrix by solving \documentclass[12pt]{minimal}
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				\begin{document}$${\textbf {data}} = {\textbf {Encode}} \times {\textbf {image}}$$\end{document}—a method referred to here as Pinv-Recon. While the benefits of this approach were acknowledged in early studies, the field has historically favored fast Fourier transforms (FFT) and iterative techniques due to perceived computational limitations of the pseudoinversion approach. This work revisits Pinv-Recon in the context of modern hardware, software, and optimized linear algebra routines. We compare various matrix inversion strategies, assess regularization effects, and demonstrate incorporation of advanced encoding physics into a unified reconstruction framework. While hardware advances have already significantly reduced computation time compared to earlier studies, our work further demonstrates that leveraging Cholesky decomposition leads to a two-order-of-magnitude improvement in computational efficiency over previous Singular Value Decomposition-based implementations. Moreover, we demonstrate the versatility of Pinv-Recon on diverse in vivo datasets encompassing a range of encoding schemes, starting with low- to medium-resolution functional and metabolic imaging and extending to high-resolution cases. Our findings establish Pinv-Recon as a versatile and robust reconstruction framework that aligns with the increasing emphasis on open-source and reproducible MRI research.

## Full-text entities

- **Genes:** SRF (serum response factor) [NCBI Gene 6722] {aka MCM1}
- **Chemicals:** Bicarbonate (MESH:D001639), Lactate (MESH:D019344), fat (MESH:D005223), Carbon-13 (MESH:C000615229), MTX (-), Pyruvate (MESH:D019289), Xe (MESH:D014978), water (MESH:D014867), Xenon-129 (MESH:C000614971)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

8 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12575614/full.md

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Source: https://tomesphere.com/paper/PMC12575614