Difference between revisions of "NA-MIC NCBC Collaboration:3D+t Cells Lineage:GoFigure"

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This Center of Excellence in Genomic Science (CEGS) assembles a multidisciplinary group of Caltech investigators, Sean Megason, Niles Pierce, Scott Fraser and Marianne Bronner-Fraser, to develop innovative technologies with the goal of imaging and mutating every developmentally important vertebrate gene. Novel "in toto imaging" tools will make it possible to analyze gene expression and function in developing vertebrate embryos in time and space, digitizing in vivo data in a systematic, high-throughput, and quantitative fashion.
 
This Center of Excellence in Genomic Science (CEGS) assembles a multidisciplinary group of Caltech investigators, Sean Megason, Niles Pierce, Scott Fraser and Marianne Bronner-Fraser, to develop innovative technologies with the goal of imaging and mutating every developmentally important vertebrate gene. Novel "in toto imaging" tools will make it possible to analyze gene expression and function in developing vertebrate embryos in time and space, digitizing in vivo data in a systematic, high-throughput, and quantitative fashion.
  
Key technologies will be developed and tested in the zebrafish embryo due to its transparency and the ability to obtain rapid feedback. To monitor alterations in gene expression in normal and mutant embryos, we will develop new techniques for in situ hybridization that permit simultaneous analysis of multiple marker genes in a sensitive and potentially quantitative manner. Our goal is to combine real-time analysis of gene expression on a genome-wide scale coupled with the ability to mutate genes of interest and examine global alterations in gene expression as a result of gene loss. The vast amount of quantitative, in vivo data obtained through this program will serve as the basis for creating a "digital fish" that models  
+
Key technologies will be developed and tested in the zebrafish embryo since
 +
it is ideal for both imaging and genetics. We are generating FlipTraps to
 +
fluorescently mark protein expression and gene function on a genome wide
 +
scale, and developing new techniques for in situ hybridization using HCR
 +
that permit simultaneous analysis of multiple marker genes. In toto imaging
 +
will be used to digitize this marked data quantitatively at cellular
 +
resolution throughout embryogenesis. The vast amount of quantitative, in
 +
vivo data obtained through this project will serve as the basis for creating
 +
a "digital fish" that models the molecular and cellular orchestra that
 +
transforms an egg into an embryo.
  
 
=== GoFigure ===
 
=== GoFigure ===

Revision as of 22:22, 16 May 2007

Home < NA-MIC NCBC Collaboration:3D+t Cells Lineage:GoFigure

Background

In Toto imaging

In Toto Genomic Analysis of Vertebrate Development

This Center of Excellence in Genomic Science (CEGS) assembles a multidisciplinary group of Caltech investigators, Sean Megason, Niles Pierce, Scott Fraser and Marianne Bronner-Fraser, to develop innovative technologies with the goal of imaging and mutating every developmentally important vertebrate gene. Novel "in toto imaging" tools will make it possible to analyze gene expression and function in developing vertebrate embryos in time and space, digitizing in vivo data in a systematic, high-throughput, and quantitative fashion.

Key technologies will be developed and tested in the zebrafish embryo since it is ideal for both imaging and genetics. We are generating FlipTraps to fluorescently mark protein expression and gene function on a genome wide scale, and developing new techniques for in situ hybridization using HCR that permit simultaneous analysis of multiple marker genes. In toto imaging will be used to digitize this marked data quantitatively at cellular resolution throughout embryogenesis. The vast amount of quantitative, in vivo data obtained through this project will serve as the basis for creating a "digital fish" that models the molecular and cellular orchestra that transforms an egg into an embryo.

GoFigure

GoFigure is an image analysis software package specifically designed for visualizing, tracking, and analyzing cells in multidimensional confocal/two-photon image sets. Eventually GoFigure will be able to analyze time-lapse series of confocal image stacks (xyzt) and to automatically segment and track cells in 2D, 2D+time, 3D, 3D+time, and 3D+time+cell division.

GoFigure now runs on the Microsoft Windows platform. GoFigure utilizes a MySql database back-end so it can handle extremely large image sets. GoFigure is build on top of ITK and VTK toolkits.

Objective:

  1. Distributed Image database
  2. Very large datasets (200+ Go)
  3. Segmentation of cells in 2D+t, 3D and 3D+t datasets
  4. Real time visualization
  5. New Data structure for 2-Manifolds (itkQE)
    1. Core
    2. Euler Operators
    3. Port of VTK filters to ITK
  6. New Data structure for 3-Manifolds
  7. New Segmentation algorithms

Progress:

  1. beta version available
  2. itkQE's core in review for integration in ITK
  3. cmake-compliant configuration/compilation
  4. packaging (cpack)
  5. Dashboard (dart2)

To Do:

Key Investigators:

  • Sean Megason (Caltech)
  • Titus Brown (Caltech)
  • Alex. Gouaillard (Caltech)

Links:

  1. Center For Excellence in Genomics (caltech)
  2. GoFigure software website
  3. GoFigure and itkQuadEdgeMesh Dashboard
  4. 4-block ppt for NAMIC Project Week will be added here