4.4 Article

A data-driven approach to optimising the encoding for multi-shell diffusion MRI with application to neonatal imaging

期刊

NMR IN BIOMEDICINE
卷 33, 期 9, 页码 -

出版社

WILEY
DOI: 10.1002/nbm.4348

关键词

diffusion MRI; HARDI; multi-shell; neonatal imaging

资金

  1. FP7 Ideas: European Research Council [319456]
  2. National Institute for Health Research
  3. Wellcome Trust [WT 203148/Z/16/Z]
  4. EPSRC [EP/L023067/1] Funding Source: UKRI
  5. MRC [MR/N026063/1] Funding Source: UKRI

向作者/读者索取更多资源

Diffusion MRI has the potential to provide important information about the connectivity and microstructure of the human brain during normal and abnormal development, noninvasively and in vivo. Recent developments in MRI hardware and reconstruction methods now permit the acquisition of large amounts of data within relatively short scan times. This makes it possible to acquire more informative multi-shell data, with diffusion sensitisation applied along many directions over multipleb-value shells. Such schemes are characterised by the number of shells acquired, and the specificb-value and number of directions sampled for each shell. However, there is currently no clear consensus as to how to optimise these parameters. In this work, we propose a means of optimising multi-shell acquisition schemes by estimating the information content of the diffusion MRI signal, and optimising the acquisition parameters for sensitivity to the observed effects, in a manner agnostic to any particular diffusion analysis method that might subsequently be applied to the data. This method was used to design the acquisition scheme for the neonatal diffusion MRI sequence used in the developing Human Connectome Project (dHCP), which aims to acquire high quality data and make it freely available to the research community. The final protocol selected by the algorithm, and currently in use within the dHCP, consists of 20b=0images and diffusion-weighted images atb= 400, 1000 and 2600 s/mm(2)with 64, 88 and 128 directions per shell, respectively.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.4
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据