Evidence map›Paper›PMID 42282214›Full record

ArticlemedRxiv : the preprint server for health sciences2026

Singular Value Decomposition-Based Coil Combination Improves the Accuracy and Noise-Robustness of Quantitative Susceptibility Maps.

Caleb Atkins, Tianxia Wu, Brandon Bujak, Souheil Inati, Peter Kellman, Govind Nair

Abstract readPreprint
In one paragraph

Article in medRxiv : the preprint server for health sciences, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Caleb AtkinsNational Institute of Neurological Disorders and Stroke, NIH, Bethesda, MD 20892, USA.ORCID 0009-0001-5105-0791
Tianxia WuNational Institute of Neurological Disorders and Stroke, NIH, Bethesda, MD 20892, USA.
Brandon BujakNational Institute of Neurological Disorders and Stroke, NIH, Bethesda, MD 20892, USA.
Souheil InatiNational Institute of Mental Health, NIH, Bethesda, MD 20892, USA.
Peter KellmanNational Heart Lung and Blood Institute, NIH, Bethesda, MD 20892, USA.
Govind NairNational Institute of Neurological Disorders and Stroke, NIH, Bethesda, MD 20892, USA.ORCID 0000-0003-3725-615X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Most high-field MRI scanners conduct imaging using phased-array coils, in which the signals received by an array of coil elements are combined for downstream processing. Optimally combining these signals requires knowledge of each coil's spatial sensitivity profile, which can be acquired from a volume coil with homogeneous sensitivity across the field-of-view. However, this approach is not often used on high-field MRI scanners, especially on non-clinical systems; therefore, this work uses an algorithm based on the singular-value decomposition (SVD), called SVD-B1, to estimate coil sensitivities directly from the array data itself. Images produced by SVD-B1 are devoid of wormhole artifacts and open-ended fringe lines commonly seen in more conventional reconstructions. Quantitative Susceptibility Maps (QSMs) produced using the algorithm were compared to those produced using other combination algorithms across clinically relevant regions of in-vivo and postmortem human brains. As progressive levels of simulated noise were added to the data, SVD-B1's QSMs were up to 3% (in-vivo) and 13% (postmortem) more consistent (as measured by their Intraclass Correlation Coefficient) than those from other algorithms. Additionally, these QSMs were up to 8.5% (in-vivo) and 36% (postmortem) more accurate than other QSMs with respect to a "single-coil" reference. A parallel imaging extension of SVD-B1, called SVD-B1 GRAPPA, achieved similar results for QSMs generated from progressively more accelerated acquisition data. These results show that SVD-B1 can improve the sensitivity of high-resolution QSM to subtle changes in fine-grained tissue structures (e.g., in neurodegenerative disease) and help reduce scan times in clinical settings where shorter scans are imperative.

Identifiers

PMID42282214
PMCPMC13252416

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.