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1.
Elife ; 52016 Mar 18.
Artigo em Inglês | MEDLINE | ID: mdl-26990779

RESUMO

Neuronal circuit mapping using electron microscopy demands laborious proofreading or reconciliation of multiple independent reconstructions. Here, we describe new methods to apply quantitative arbor and network context to iteratively proofread and reconstruct circuits and create anatomically enriched wiring diagrams. We measured the morphological underpinnings of connectivity in new and existing reconstructions of Drosophila sensorimotor (larva) and visual (adult) systems. Synaptic inputs were preferentially located on numerous small, microtubule-free 'twigs' which branch off a single microtubule-containing 'backbone'. Omission of individual twigs accounted for 96% of errors. However, the synapses of highly connected neurons were distributed across multiple twigs. Thus, the robustness of a strong connection to detailed twig anatomy was associated with robustness to reconstruction error. By comparing iterative reconstruction to the consensus of multiple reconstructions, we show that our method overcomes the need for redundant effort through the discovery and application of relationships between cellular neuroanatomy and synaptic connectivity.


Assuntos
Conectoma/métodos , Drosophila/anatomia & histologia , Drosophila/fisiologia , Animais , Sistema Nervoso/anatomia & histologia , Fenômenos Fisiológicos do Sistema Nervoso
2.
PLoS One ; 7(6): e38011, 2012.
Artigo em Inglês | MEDLINE | ID: mdl-22723842

RESUMO

A key challenge in neuroscience is the expeditious reconstruction of neuronal circuits. For model systems such as Drosophila and C. elegans, the limiting step is no longer the acquisition of imagery but the extraction of the circuit from images. For this purpose, we designed a software application, TrakEM2, that addresses the systematic reconstruction of neuronal circuits from large electron microscopical and optical image volumes. We address the challenges of image volume composition from individual, deformed images; of the reconstruction of neuronal arbors and annotation of synapses with fast manual and semi-automatic methods; and the management of large collections of both images and annotations. The output is a neural circuit of 3d arbors and synapses, encoded in NeuroML and other formats, ready for analysis.


Assuntos
Modelos Neurológicos , Rede Nervosa , Software , Transmissão Sináptica/fisiologia , Animais , Neuroimagem , Neurônios , Sinapses
3.
Nat Methods ; 9(7): 676-82, 2012 Jun 28.
Artigo em Inglês | MEDLINE | ID: mdl-22743772

RESUMO

Fiji is a distribution of the popular open-source software ImageJ focused on biological-image analysis. Fiji uses modern software engineering practices to combine powerful software libraries with a broad range of scripting languages to enable rapid prototyping of image-processing algorithms. Fiji facilitates the transformation of new algorithms into ImageJ plugins that can be shared with end users through an integrated update system. We propose Fiji as a platform for productive collaboration between computer science and biology research communities.


Assuntos
Biologia Computacional/métodos , Processamento de Imagem Assistida por Computador/métodos , Software , Algoritmos , Animais , Encéfalo/ultraestrutura , Drosophila melanogaster/ultraestrutura , Aumento da Imagem/métodos , Imageamento Tridimensional/métodos , Disseminação de Informação , Design de Software
4.
Bioinformatics ; 27(17): 2453-4, 2011 Sep 01.
Artigo em Inglês | MEDLINE | ID: mdl-21727141

RESUMO

MOTIVATION: Advances in techniques to sparsely label neurons unlock the potential to reconstruct connectivity from 3D image stacks acquired by light microscopy. We present an application for semi-automated tracing of neurons to quickly annotate noisy datasets and construct complex neuronal topologies, which we call the Simple Neurite Tracer. AVAILABILITY: Simple Neurite Tracer is open source software, licensed under the GNU General Public Licence (GPL) and based on the public domain image processing software ImageJ. The software and further documentation are available via http://fiji.sc/Simple_Neurite_Tracer as part of the package Fiji, and can be used on Windows, Mac OS and Linux. Documentation and introductory screencasts are available at the same URL. CONTACT: longair@ini.phys.ethz.ch; longair@ini.phys.ethz.ch.


Assuntos
Neuritos/ultraestrutura , Neurônios/citologia , Software , Animais , Gráficos por Computador , Humanos , Processamento de Imagem Assistida por Computador , Imageamento Tridimensional
5.
Database (Oxford) ; 2010: baq005, 2010 Jul 06.
Artigo em Inglês | MEDLINE | ID: mdl-20624714

RESUMO

Protein-trap strains of Drosophila melanogaster provide a very useful tool for examining the 3D-expression patterns of proteins and purification of protein complexes. Here we present BrainTrap, available at http://fruitfly.inf.ed.ac.uk/braintrap, an online database of 3D confocal datasets showing reporter gene expression and protein localization in the adult brain of Drosophila. Full size images throughout the volume of the entire brain can be viewed interactively in a web browser. The database includes searchable annotations linked to the FlyBase Drosophila anatomy ontology. Anatomical search criteria can be specified using automatic completion and a hierarchical browser for the ontology. The provenance of all annotation is retained and the location where the annotator made the conclusion can be highlighted. Database URL: http://fruitfly.inf.ed.ac.uk/braintrap.


Assuntos
Encéfalo/anatomia & histologia , Encéfalo/metabolismo , Bases de Dados de Proteínas , Proteínas de Drosophila/genética , Proteínas de Drosophila/metabolismo , Drosophila melanogaster/genética , Drosophila melanogaster/metabolismo , Animais , Drosophila melanogaster/anatomia & histologia , Perfilação da Expressão Gênica/estatística & dados numéricos , Genes de Insetos , Imageamento Tridimensional , Proteínas do Tecido Nervoso/genética , Proteínas do Tecido Nervoso/metabolismo , Distribuição Tecidual
6.
BMC Bioinformatics ; 11: 274, 2010 May 21.
Artigo em Inglês | MEDLINE | ID: mdl-20492697

RESUMO

BACKGROUND: Current imaging methods such as Magnetic Resonance Imaging (MRI), Confocal microscopy, Electron Microscopy (EM) or Selective Plane Illumination Microscopy (SPIM) yield three-dimensional (3D) data sets in need of appropriate computational methods for their analysis. The reconstruction, segmentation and registration are best approached from the 3D representation of the data set. RESULTS: Here we present a platform-independent framework based on Java and Java 3D for accelerated rendering of biological images. Our framework is seamlessly integrated into ImageJ, a free image processing package with a vast collection of community-developed biological image analysis tools. Our framework enriches the ImageJ software libraries with methods that greatly reduce the complexity of developing image analysis tools in an interactive 3D visualization environment. In particular, we provide high-level access to volume rendering, volume editing, surface extraction, and image annotation. The ability to rely on a library that removes the low-level details enables concentrating software development efforts on the algorithm implementation parts. CONCLUSIONS: Our framework enables biomedical image software development to be built with 3D visualization capabilities with very little effort. We offer the source code and convenient binary packages along with extensive documentation at http://3dviewer.neurofly.de.


Assuntos
Interpretação de Imagem Assistida por Computador/métodos , Imageamento Tridimensional/métodos , Linguagens de Programação , Gráficos por Computador , Microscopia Confocal/métodos , Reconhecimento Automatizado de Padrão/métodos , Software
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