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Facilities & Resources |
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The Beagle Genome Annotation
Database
Beagle is a human-centered database designed as a tool
for biological discovery and exploration. The 2.4 GB database,
which includes build-in software, has records for all
~245,000 Homo sapiens, Pan troglodytes, Canis lupus familiaris,
Mus musculus, Danio rerio, Drosophila melanogaster, Caenorhabditis
elegans, Saccharomyces cerevisiae, and Schizosaccharomyces
pombe genes.
Guided
Tour and More Information |
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CHGR Clinical Genetic
Research Facility
The facility's primary mission is to support and promote
genetic clinical research. It provides an infrastructure
and space where clinical investigators can study disease
states and collect specimens for their genetic research.
Services,
Facilities & Equipment, Contact Information |
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CHGR DNA and Tissue Culture
Resource
This facility provides processing of cell lines, human
blood and tissue samples for DNA, plasma and buffy coat
storage and for initiation of lymphoblast and fibroblast
cell lines in furtherance of the CHGR mission to promote
the use of genetic strategies in basic and clinical research.
Services,
Facilities & Equipment, Contact Information |
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CHGR Genotyping Resource
Genotyping is performed for determining genetic variation
in man and mouse, of interest for studies of human health
and disease.
Services,
Facilities & Equipment, Contact Information |
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CHGR
Monoclonal Antibody Production Facility
This Facility provides a monoclonal antibody production
service to research projects. Protein/peptides provided
by the individual investigators will be used to generate
mouse monoclonal antibodies.
Services,
Facilities & Equipment, Contact Information
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C57BL/J
A/J
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CHGR Chromosome
Substitution Strain (CSS) Resource
The C57BL6/J and A/J strains exhibit inherited variation
in many phenotypes of interest for human disease, including
physiology, metabolism, susceptibility or resistance to
spontaneous diseases, such as arthritis, atherosclerosis
and cancer, as well as differences in susceptibility or
resistance to infection and inflammation.
A panel of 22 related inbred C57BL/6 lines each homozygous
for a different A/J chromosome (19 autosomes, X, Y, mitochondria),
called a chromosome substitution strain set, provides
a tool for studies, to identify genetic variation that
contributes to complex phenotypes of interest to human
health and disease.
Services,
Facilities & Equipment, Contact Information |
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