21,808 research outputs found
Multi-site genetic analysis of diffusion images and voxelwise heritability analysis : a pilot project of the ENIGMA–DTI working group
The ENIGMA (Enhancing NeuroImaging Genetics through Meta-Analysis) Consortium was set up to analyze brain measures and genotypes from multiple sites across the world to improve the power to detect genetic variants that influence the brain. Diffusion tensor imaging (DTI) yields quantitative measures sensitive to brain development and degeneration, and some common genetic variants may be associated with white matter integrity or connectivity. DTI measures, such as the fractional anisotropy (FA) of water diffusion, may be useful for identifying genetic variants that influence brain microstructure. However, genome-wide association studies (GWAS) require large populations to obtain sufficient power to detect and replicate significant effects, motivating a multi-site consortium effort. As part of an ENIGMA–DTI working group, we analyzed high-resolution FA images from multiple imaging sites across North America, Australia, and Europe, to address the challenge of harmonizing imaging data collected at multiple sites. Four hundred images of healthy adults aged 18–85 from four sites were used to create a template and corresponding skeletonized FA image as a common reference space. Using twin and pedigree samples of different ethnicities, we used our common template to evaluate the heritability of tract-derived FA measures. We show that our template is reliable for integrating multiple datasets by combining results through meta-analysis and unifying the data through exploratory mega-analyses. Our results may help prioritize regions of the FA map that are consistently influenced by additive genetic factors for future genetic discovery studies. Protocols and templates are publicly available at (http://enigma.loni.ucla.edu/ongoing/dti-working-group/)
An automated workflow for parallel processing of large multiview SPIM recordings
Multiview light sheet fluorescence microscopy (LSFM) allows to image
developing organisms in 3D at unprecedented temporal resolution over long
periods of time. The resulting massive amounts of raw image data requires
extensive processing interactively via dedicated graphical user interface (GUI)
applications. The consecutive processing steps can be easily automated and the
individual time points can be processed independently, which lends itself to
trivial parallelization on a high performance cluster (HPC). Here we introduce
an automated workflow for processing large multiview, multi-channel,
multi-illumination time-lapse LSFM data on a single workstation or in parallel
on a HPC. The pipeline relies on snakemake to resolve dependencies among
consecutive processing steps and can be easily adapted to any cluster
environment for processing LSFM data in a fraction of the time required to
collect it.Comment: 13 pages with supplement, LATEX; 1 table, 1 figure, 2 supplementary
figures, 2 supplementary lists, 2 supplementary tables; corrected error in
results table, results unchange
The INCF Digital Atlasing Program: Report on Digital Atlasing Standards in the Rodent Brain
The goal of the INCF Digital Atlasing Program is to provide the vision and direction necessary to make the rapidly growing collection of multidimensional data of the rodent brain (images, gene expression, etc.) widely accessible and usable to the international research community. This Digital Brain Atlasing Standards Task Force was formed in May 2008 to investigate the state of rodent brain digital atlasing, and formulate standards, guidelines, and policy recommendations.

Our first objective has been the preparation of a detailed document that includes the vision and specific description of an infrastructure, systems and methods capable of serving the scientific goals of the community, as well as practical issues for achieving
the goals. This report builds on the 1st INCF Workshop on Mouse and Rat Brain Digital Atlasing Systems (Boline et al., 2007, _Nature Preceedings_, doi:10.1038/npre.2007.1046.1) and includes a more detailed analysis of both the current state and desired state of digital atlasing along with specific recommendations for achieving these goals
Towards segmentation and spatial alignment of the human embryonic brain using deep learning for atlas-based registration
We propose an unsupervised deep learning method for atlas based registration
to achieve segmentation and spatial alignment of the embryonic brain in a
single framework. Our approach consists of two sequential networks with a
specifically designed loss function to address the challenges in 3D first
trimester ultrasound. The first part learns the affine transformation and the
second part learns the voxelwise nonrigid deformation between the target image
and the atlas. We trained this network end-to-end and validated it against a
ground truth on synthetic datasets designed to resemble the challenges present
in 3D first trimester ultrasound. The method was tested on a dataset of human
embryonic ultrasound volumes acquired at 9 weeks gestational age, which showed
alignment of the brain in some cases and gave insight in open challenges for
the proposed method. We conclude that our method is a promising approach
towards fully automated spatial alignment and segmentation of embryonic brains
in 3D ultrasound
OpenSPIM - an open access platform for light sheet microscopy
Light sheet microscopy promises to revolutionize developmental biology by
enabling live in toto imaging of entire embryos with minimal phototoxicity. We
present detailed instructions for building a compact and customizable Selective
Plane Illumination Microscopy (SPIM) system. The integrated OpenSPIM hardware
and software platform is shared with the scientific community through a public
website, thereby making light sheet microscopy accessible for widespread use
and optimization to various applications.Comment: 7 pages, 3 figures, 6 supplementary videos, submitted to Nature
Methods, associated public website http://openspim.or
Fast fluorescence microscopy for imaging the dynamics of embryonic development
Live imaging has gained a pivotal role in developmental biology since it increasingly allows real-time observation of cell behavior in intact organisms. Microscopes that can capture the dynamics of ever-faster biological events, fluorescent markers optimal for in vivo imaging, and, finally, adapted reconstruction and analysis programs to complete data flow all contribute to this success. Focusing on temporal resolution, we discuss how fast imaging can be achieved with minimal prejudice to spatial resolution, photon count, or to reliably and automatically analyze images. In particular, we show how integrated approaches to imaging that combine bright fluorescent probes, fast microscopes, and custom post-processing techniques can address the kinetics of biological systems at multiple scales. Finally, we discuss remaining challenges and opportunities for further advances in this field
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