NOD-scid IL2rgnull (NSG) and NOD-Rag1null IL2rgnull (NRG) mice support heightened levels of engraftment with human cells and tissues. These engrafted mice allow research on human disease processes without putting individuals at risk.
Tools for automatic glomerulus identification and histological quantification from scanned PAS slides
Phenotype and RNAseq data from approx. 200 (B6-Col4a5 KO x DO)F1 mice
Resource lists and describes mouse models for ocular research at JAX.
Professor, Karl Gunnar Johansson Chair
Genetic Resource Science initiates and develops resource-generating research. Our team: identifies and implements innovative technologies for genetic research; makes and distributes new mouse models; and provides extensive genetic and phenotypic information on JAX mouse strains.
This tool calculates the glomerular filtration rate in mice using the FITC-inulin method
Utilizing genomic approaches to interrogate mechanisms of inherited cardiovascular disorders.
Integrating multi-track Hi-C data for genome-scale reconstruction of 3D chromatin structure
ATAC-seq is a new protocol to capture open chromatin sites by performing adaptor ligation and fragmentation of open chromatin regions. Due to its efficiency in requirement of biological sample and in library preparation time, many scientists are generating ATAC-seq libraries to decipher the chromatin landscape of DNA in a given cell type and condition of interest.
The JAX Cre Repository's aim is to provide the scientific community with a centralized, comprehensive set of well-characterized Cre-driver lines and related information resources.
Associate Research Scientist
Scientists around the world are working to generate a targeted knockout mutation for every gene in the mouse genome through the Knockout Mouse Project (KOMP) which is providing critical tools for understanding gene function and the genetic causes of human diseases.
MAV-seq (Management, Analysis, Visualization of Sequence data) is an interactive, user friendly, cross platform, secure, encrypted, automated, customized, centralized, multi-roles based database application for the management of sample repertoires and automation of the data pre-processing of epigenomic and transcriptomic data.
Mice harboring spontaneous mutations have long been a major source for animal models of human genetic disorders, particularly mendelian diseases. The Mouse Mutant Resource maintains over 700 established mutant strains.
This resource provides mouse models for facial, dental, eye, ear and skull development research, as well as mouse models of human craniofacial syndromes.
The Mouse Tumor Biology (MTB) Database supports the use of the mouse as a model system of hereditary cancer by electronic access to a variety of information.
Models genome regulation using computational and statistical methods.
The Parkinson’s Disease Mouse Model Resource characterizes and distributes new mouse models of Parkinsonism and Parkinson’s disease.
The SMSR maintains mice that are important tools for genetic analysis of complex diseases, including consomic strains.
A tool for novel Least Diverged Ortholog prediction through machine learning