 |
|
 |
|
Aplysia EST Project:
http://aplysia.cu-genome.org/html/index.html
(password protected)
Genomic Science Centers
Funded by NIH
|
Berkley Molecular Sciences Institute
-- Center for Genomic Experimentation and
Computation
We will
establish a center that combines functional genomic and computational
research to model a prototype signal transduction pathway. Work at the
center will focus on the "Alpha Project." The overall goal of the work
is to gain the ability to predict the behavior of a well-studied
biological regulatory system at the level of individual cells.
|
|
Harvard
University -- Molecular and Genomic
Imaging Center
We propose here
the Molecular and Genomic Imaging Center (MGIC) in response to a
biomedical-community-wide need for flexible, cost-effective,
high-resolution technology to identify and characterize variation in
biological systems at the level of genomes and transcriptomes.
|
|
Johns Hopkins University -- Center
for the Epigenetics of Common Human Disease
Epigenetics is
the study of information within the cell that is heritable during cell
division, but does not lie within the DNA sequence itself. Epigenetics
has been largely ignored in human genomic science, although there is
reason to believe that common human diseases may be related to
epigenetic modifiers.
|
|
Yale
University -- Human Genome Array:
Technology for Functional Analysis
We propose to
establish a center to build genomic DNA arrays and develop novel
technologies that will use these arrays for the large-scale functional
analysis of the human genome. 0.3-1.4 kb fragments of nonrepetitive DNA
from each of chromosomes 22, 21, 20, 19,7, 17, and perhaps the X
chromosome will be prepared by PCR and attached to microscope slides.
|
University of Southern California -- Implications
of Haplotype Structure in the Human Genome
Recent studies
have
indicated that human genetic variation has a "haplotype block
structure" such that each chromosome can be decomposed into large
blocks with strong linkage disequilibrium (LD) and relatively few
haplotypes, separated by short regions of extensive recombination. The
primary objective of this application is to study the biological
significance of the observed haplotype structure and the practical
implications of such haplotype structure for the mapping of genes
responsible for human disease. |
| NIH CEGS [ 2001-2006
] |
|
|
|
|
|
|
 |