arXiv subjects

Markus Barth

Publications and source records attributed to Markus Barth.

4 recordsLinked to original sources

arXiv2021

NeXtQSM -- A complete deep learning pipeline for data-consistent quantitative susceptibility mapping trained with hybrid data

Deep learning based Quantitative Susceptibility Mapping (QSM) has shown great potential in recent years, obtaining similar results to established non-learning approaches. Many current deep learning approaches are not data consistent, require in vivo training data or solve the QSM problem in consecutive steps resulting in the propagation of errors. Here we aim to overcome these limitations and developed a framework to solve the QSM processing steps jointly. We developed a new hybrid training data generation method that enables the end-to-end training for solving background field correction and dipole inversion in a data-consistent fashion using a variational network that combines the QSM model term and a learned regularizer. We demonstrate that NeXtQSM overcomes the limitations of previous deep learning methods. NeXtQSM offers a new deep learning based pipeline for computing quantitative susceptibility maps that integrates each processing step into the training and provides results that are robust and fast.

eess.IV↗

arXiv2019

Improving FLAIR SAR efficiency at 7T by adaptive tailoring of adiabatic pulse power using deep convolutional neural networks

Purpose: The purpose of this study is to demonstrate a method for Specific Absorption Rate (SAR) reduction for T2-FLAIR MRI sequences at 7T by predicting the required adiabatic pulse power and scaling the amplitude in a slice-wise fashion. Methods: We used a TR-FOCI adiabatic pulse for spin inversion in a T2-FLAIR sequence to improve B1+ homogeneity and calculate the pulse power required for adiabaticity slice-by-slice to minimize the SAR. Drawing on the implicit B1+ inhomogeneity present in a standard localizer scan, 3D AutoAlign localizers and SA2RAGE B1+ maps were acquired in eight volunteers. A convolutional neural network (CNN) was then trained to predict the B1+ profile from the localizers and scale factors for the pulse power for each slice were calculated. The ability to predict the B1+ profile as well as how the derived pulse scale factors affected the FLAIR inversion efficiency were assessed in transverse, sagittal, and coronal orientations. Results: The predicted B1+ maps matched the measured B1+ maps with a mean difference of 4.45% across all slices. The acquisition in the transverse orientation was shown to be most effective for this method and delivered a 40% reduction in SAR along with 1min and 30-sec reduction in scan time (28%) without degradation of image quality. Conclusion: We propose a SAR reduction technique based on the prediction of B1+ profiles from standard localizer scans using a CNN and show that scaling the inversion pulse power slice-by-slice for FLAIR sequences at 7T reduces SAR and scan time without compromising image quality.

eess.IV↗

arXiv2017

Serial Correlations in Single-Subject fMRI with Sub-Second TR

When performing statistical analysis of single-subject fMRI data, serial correlations need to be taken into account to allow for valid inference. Otherwise, the variability in the parameter estimates might be under-estimated resulting in increased false-positive rates. Serial correlations in fMRI data are commonly characterized in terms of a first-order autoregressive (AR) process and then removed via pre-whitening. The required noise model for the pre-whitening depends on a number of parameters, particularly the repetition time (TR). Here we investigate how the sub-second temporal resolution provided by simultaneous multislice (SMS) imaging changes the noise structure in fMRI time series. We fit a higher-order AR model and then estimate the optimal AR model order for a sequence with a TR of less than 600 ms providing whole brain coverage. We show that physiological noise modelling successfully reduces the required AR model order, but remaining serial correlations necessitate an advanced noise model. We conclude that commonly used noise models, such as the AR(1) model, are inadequate for modelling serial correlations in fMRI using sub-second TRs. Rather, physiological noise modelling in combination with advanced pre-whitening schemes enable valid inference in single-subject analysis using fast fMRI sequences.

stat.AP↗

arXiv2002

Fractal noise maps reveal human brain activity: a key for unbiased fMRI analysis

Brain metabolism is controlled by complex regulation mechanisms. As part of their nature many complex systems show scaling behavior in their timeseries data. Corresponding scaling exponents can sometimes be used to characterize these systems. Here we present maps of scaling exponents derived from BOLD functional Magnetic Resonance Imaging (fMRI) data, and show that they reveal activation patterns in the human brain with very high precision. In contrast to standard model-based analysis we use no prior knowledge on the experimental stimulation paradigm for extracting activation patterns from fMRI timeseries. We demonstrate that mental activity is one-to-one related to large fractal exponents, or equivalently, to temporally highly correlated processes.

cond-mat↗