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About the 
The Cell Centered Database or CCDB was created to house the types of
high resolution 3D light and electron microscopic reconstructions
produced at the National Center for
Microscopy and Imaging Research. It contains structural and
protein distribution information derived from confocal, multiphoton
and electron microscopy, including correlated microscopy. Many of the
data sets are derived from
electron
tomography. Electron tomography is similar in concept to medical
imaging techniques like CAT scans and MRI in that it derives a 3D
volume from a series of 2D projections through a structure. In this
case, the structures are contained in sections prepared for electron
microscopy which are tilted through a limited angular range. Many of
the data sets in the CCDB come from studies of the nervous system,
although the CCDB is not restricted to neuronal information.
Additional information on some of the tomography projects underway at
NCMIR can be found
here. The CCDB is
built on an object-relational framework using Oracle 9i. The current
CCDB has over 80 tables containing a large amount of descriptive data.
The simplified schema may be viewed here. The
CCDB is built around 3D reconstructions performed at the light and
electron microscopic levels, including correlated datasets. It models
the entire process of reconstruction, from specimen preparation to
segmentation and analysis. A volume reconstruction is stored along
with pointers to all of the raw images and the processing details
required to reconstruct the volume from the raw data. Each object
that is segmented from the 3D volume is stored as a separate object
indexed to the parent reconstruction. Four types of segmented objects
are currently modeled in the CCDB:
- surface objects : polygonal surface meshes representing
3D objects in the reconstruction, extracted using either
isosurfacing methods or manual contouring
- contour objects : a series of contours that have not
been fitted with a surface
- volume objects : subvolumes containing an object of
interest
- tree objects: skeletons of branching objects like
dendrites and axons, derived from Neurolucida
(Microbrightfield, Inc., VT)
Each object is stored along with any measurements like surface area,
volume, length, number and labeling intensity. Whenever possible,
parsers are written for the output of analysis programs so that
results can be uploaded directly into the CCDB. For example,
measurement summaries for tree objects are uploaded directly from the
output of NeuroExplorer, an analysis program for Neurolucida derived
data.
Rationale
The rationale behind creating the CCDB as a publically accessible data
base is to provide a resource to the structural biology and
neuroscience communities. First, we wanted a venue for disseminated
the very rich and unique datasets acquired by electron tomography.
Because of the superior resolution of tomographic datasets, they often
contain much more data than is analyzed by a single researcher. A
single electron tomographic study generally relies on a very small
sample size because of the labor involved in acquiring and analyzing
the specimens. Thus, having a repository where these data sets can be
accumulated and reanalyzed will help researchers gain a better picture
of variation across structures. Because of the labor intensive nature
of the process, tomographers are constantly looking at new algorithms
for segmenting and visualizing data. Thus, the CCDB can serve as a
resource for those involved in these pursuits. Finally, the CCDB
serves a resource for researchers interested in computational modeling
of cells and the cellular microenvironment. The CCDB contains many
individual neurons that have been skeletonized in a form usable by
modeling programs such as Genesis and Neuron. Tomographic
reconstructions are serving as the basis for sophisticated modeling
studies on molecular dynamics in the cellular microenvironment.
Simplified Schema

Entity-Relationship (ER)
Diagram
The ER diagram (approx 1.5 MB)
represents the schema as of September 24th, 2003.
Data Entry
For a description of how files are managed in the CCDB and how to
prepare files for entry, see this page.
Future Development
Plans
- In future versions of the CCDB, users will have access to more
advanced query forms which take advantage of the rich data model
of the CCDB. An example of such a query can be found
here.
- Future plans also include the implementation of an atlas-based
interface and implementation of a knowledge-based query system.
More information on this can be found at the
"Federation of Brain
Data" and BIRN sites. A
demonstration of the "Smart Atlas" is given in this
Powerpoint presentation.
Project Team Members
- Leaders:
- Maryann Martone
- Amarnath Gupta
- Mark Ellisman
- Database design and implementation:
- Yujun Wang
- Julia Sun
- Xufei Qian
- Web design:
- Contributors:
- Diana Price
- Masako Terada
- Andrea Thor
Publications
- Shenglan Zhang, Xufei Qian, Amarnath Gupta, Maryann E. Martone.
A Practical Approach for Microscopy Imaging Data Management (MIDM) in
Neuroscience. 15th International Conference on Scientific and
Statistical Database Management (SSDBM 2003) July 9-11 Cambridge,
Massachusetts, 2003.
- Shenglan Zhang, Diana Price, Xufei Qian, Amarnath Gupta, Mark H.
Ellisman, Maryann E. Martone. A Cell Centered Database (CCDB) for
Multi-Scale Microscopy Data Management. Microscopy and Microanalysis
2003 (M&M 2003) August 3-7 San Antonio, Texas, 2003.
- Martone, M. E., Gupta, A., Wong, M., Qian, X., Sosinsky, G.,
Ludaescher, B., and Ellisman, M. H. A cell centered database
for electron tomographic data. J. Struct. Biology 138:
145-155, 2002.
- Martone, M. E., Gupta, A. Qian, X., Wong, M., Zhang, S.,
Ludaescher, B., Zaslavsky, I. , D. Martinez-Price and Ellisman,
M. H. The cell-centered database: an online resource for high
resolution cell level data, Soc. for Neurosci. Abstr.,
2002. [PDF : 423KB,
1.57MB,
4.1MB]
- Martone, M. E., Gupta, A., Ludascher, Zaslavsky, I. and
Ellisman, M. H. Federation of brain data through
knowledge-guided mediation. In Kotter, R. Neuroscience
Databases: a Practical Guide, Boston: Kluwer Academic Press,
275-292, 2002.
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