dHCP

dHCP constructs a detailed 4-dimensional connectome of the developing human brain between 20-45 weeks post-menstrual age using multi-modal MRI, including in utero and ex utero neonatal fMRI from over 1,000 subjects.


Key Features:

  • Automated resting-state functional processing framework: A pipeline tailored for neonatal fMRI that addresses low and variable tissue contrast and high head motion.
  • Integrated Slice-to-Volume Motion Correction: Corrects motion artifacts prevalent in neonatal datasets to improve spatial alignment of fMRI slices.
  • Dynamic Susceptibility Distortion Correction: Reduces distortions from magnetic field inhomogeneities to enhance image fidelity.
  • Robust Multimodal Registration Approach: Ensures precise alignment across different imaging modalities for integrated analysis.
  • Bespoke ICA-based Denoising: Uses Independent Component Analysis to separate signal from noise and improve detection of resting-state networks (RSNs).
  • Automated Quality Control Framework: Provides rigorous quality assurance to minimize failure rates and select high-quality data for analysis.
  • Large multi-modal neonatal cohort: Processes data from over 1,000 subjects scanned in utero and ex utero across 20-45 weeks post-menstrual age.
  • Cohort-level performance improvements: Demonstrated increases in signal-to-noise ratio (SNR) and detection of high-quality RSNs on a large evaluated cohort.

Scientific Applications:

  • 4D developing human connectome construction: Enables mapping of structural and functional connectivity changes over 20-45 weeks post-menstrual age.
  • Neonatal resting-state network analysis: Facilitates identification and characterization of RSNs in early life using denoised, motion- and distortion-corrected fMRI.
  • Developmental neuroimaging studies: Provides quality-controlled multi-modal MRI data for studies of brain development in utero and ex utero.
  • Method validation and cohort analyses: Supports evaluation of preprocessing strategies via cohort-level SNR and RSN detection metrics.

Methodology:

Processing steps include integrated slice-to-volume motion correction, dynamic susceptibility distortion correction, robust multimodal registration, bespoke ICA-based denoising, and an automated quality control framework.

Topics

Details

License:
Apache-2.0
Tool Type:
workflow
Added:
11/14/2019
Last Updated:
11/24/2024

Operations

Publications

Fitzgibbon SP, Harrison SJ, Jenkinson M, Baxter L, Robinson EC, Bastiani M, Bozek J, Karolis V, Cordero Grande L, Price AN, Hughes E, Makropoulos A, Passerat-Palmbach J, Schuh A, Gao J, Farahibozorg S, O'Muircheartaigh J, Ciarrusta J, O'Keeffe C, Brandon J, Arichi T, Rueckert D, Hajnal JV, Edwards AD, Smith SM, Duff E, Andersson J. The developing Human Connectome Project (dHCP) automated resting-state functional processing framework for newborn infants. NeuroImage. 2020;223:117303. doi:10.1016/j.neuroimage.2020.117303. PMID:32866666. PMCID:PMC7762845.

PMID: 32866666
PMCID: PMC7762845
Funding: - Wellcome Trust: 203139/ Z/16/Z - Medical Research Council: 098369/Z/12/Z, MR/P008712/1 - Royal Society: 1U01AG052564–0 1, 2017–403, 206675/Z/17/Z - National Institutes of Health: 1U01AG052564–01, 1U01MH109589–01, 215573/Z/19 - Seventh Framework Programme: FP/20072013 - European Regional Development Fund: KK.01.1.1.01.0009 - European Research Council: 319456

Fitzgibbon SP, Harrison SJ, Jenkinson M, Baxter L, Robinson EC, Bastiani M, Bozek J, Karolis V, Grande LC, Price AN, Hughes E, Makropoulos A, Passerat-Palmbach J, Schuh A, Gao J, Farahibozorg S, O’Muircheartaigh J, Ciarrusta J, O’Keeffe C, Brandon J, Arichi T, Rueckert D, Hajnal JV, Edwards AD, Smith SM, Duff E, Andersson J. The developing Human Connectome Project (dHCP) automated resting-state functional processing framework for newborn infants. Unknown Journal. 2019. doi:10.1101/766030.

Links