arXiv subjects

Yogesh Rathi

Publications and source records attributed to Yogesh Rathi.

57 records · Page 4Linked to original sources

arXiv2020

High-fidelity, accelerated whole-brain submillimeter in-vivo diffusion MRI using gSlider-Spherical Ridgelets (gSlider-SR)

Purpose: To develop an accelerated, robust, and accurate diffusion MRI acquisition and reconstruction technique for submillimeter whole human brain in-vivo scan on a clinical scanner. Methods: We extend the ultra-high resolution diffusion MRI acquisition technique, gSlider, by allowing under-sampling in q-space and Radio-Frequency (RF)-encoded data, thereby accelerating the total acquisition time of conventional gSlider. The novel method, termed gSlider-SR, compensates for the lack of acquired information by exploiting redundancy in the dMRI data using a basis of Spherical Ridgelets (SR), while simultaneously enhancing the signal-to-noise ratio. Using Monte-Carlo simulation with realistic noise levels and several acquisitions of in-vivo human brain dMRI data (acquired on a Siemens Prisma 3T scanner), we demonstrate the efficacy of our method using several quantitative metrics. Results: For high-resolution dMRI data with realistic noise levels (synthetically added), we show that gSlider-SR can reconstruct high-quality dMRI data at different acceleration factors preserving both signal and angular information. With in-vivo data, we demonstrate that gSlider-SR can accurately reconstruct 860 $μm$ diffusion MRI data (64 diffusion directions at b = 2000 $s/ {mm}^2$), at comparable quality as that obtained with conventional gSlider with four averages, thereby providing an eight-fold reduction in scan time (from 1 h 20 min to 10 min). Conclusion: gSlider-SR enables whole-brain high angular resolution dMRI at a submillimeter spatial resolution with a dramatically reduced acquisition time, making it feasible to use the proposed scheme on existing clinical scanners.

eess.IV↗

arXiv2015

The White Matter Query Language: A Novel Approach for Describing Human White Matter Anatomy

We have developed a novel method to describe human white matter anatomy using an approach that is both intuitive and simple to use, and which automatically extracts white matter tracts from diffusion MRI volumes. Further, our method simplifies the quantification and statistical analysis of white matter tracts on large diffusion MRI databases. This work reflects the careful syntactical definition of major white matter fiber tracts in the human brain based on a neuroanatomist's expert knowledge. The framework is based on a novel query language with a near-to-English textual syntax. This query language makes it possible to construct a dictionary of anatomical definitions that describe white matter tracts. The definitions include adjacent gray and white matter regions, and rules for spatial relations. This novel method makes it possible to automatically label white matter anatomy across subjects. After describing this method, we provide an example of its implementation where we encode anatomical knowledge in human white matter for 10 association and 15 projection tracts per hemisphere, along with 7 commissural tracts. Importantly, this novel method is comparable in accuracy to manual labeling. Finally, we present results applying this method to create a white matter atlas from 77 healthy subjects, and we use this atlas in a small proof-of-concept study to detect changes in association tracts that characterize schizophrenia.

q-bio.NC↗

arXiv2010

Spatially regularized compressed sensing of diffusion MRI data

The present paper introduces a method for substantial reduction of the number of diffusion encoding gradients required for reliable reconstruction of HARDI signals. The method exploits the theory of compressed sensing (CS), which establishes conditions on which a signal of interest can be recovered from its under-sampled measurements, provided that the signal admits a sparse representation in the domain of a linear transform. In the case at hand, the latter is defined to be spherical ridgelet transformation, which excels in sparsifying HARDI signals. What makes the resulting reconstruction procedure even more accurate is a combination of the sparsity constraints in the diffusion domain with additional constraints imposed on the estimated diffusion field in the spatial domain. Accordingly, the present paper describes a novel way to combine the diffusion- and spatial-domain constraints to achieve a maximal reduction in the number of diffusion measurements, while sacrificing little in terms of reconstruction accuracy. Finally, details are provided on a particularly efficient numerical scheme which can be used to solve the aforementioned reconstruction problem by means of standard and readily available estimation tools. The paper is concluded with experimental results which support the practical value of the proposed reconstruction methodology.

cs.IT↗