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Updated: Apr 11, 2026

Mouse Genome Engineering Using Designer Nucleases
Published on: April 2, 2014
NIG_MoG: a mouse genome navigator for exploring intersubspecific genetic polymorphisms.
Toyoyuki Takada1, Atsushi Yoshiki, Yuichi Obata
1Mammalian Genetics Laboratory, National Institute of Genetics, 1111 Yata, Mishima, Shizuoka, 411-8540, Japan, ttakada@nig.ac.jp.
The National Institute of Genetics Mouse Genome database (NIG_MoG) visualizes genome differences in Japanese mouse strains (Mus musculus molossinus). This resource aids researchers in exploring mouse genome variations and bacterial artificial chromosome clones.
Area of Science:
- Genomics
- Bioinformatics
- Comparative genomics
Background:
- The National Institute of Genetics Mouse Genome database (NIG_MoG) houses whole-genome sequence data for MSM/Ms and JF1/Ms mouse strains.
- These strains originate from the Japanese subspecies Mus musculus molossinus.
- Understanding intersubspecific genome divergence is crucial for genetic research.
Purpose of the Study:
- To provide visualized genome polymorphism information for MSM/Ms and JF1/Ms mouse strains.
- To facilitate the in silico screening of bacterial artificial chromosome (BAC) clones.
- To serve as a resource for exploring mouse genome polymorphisms and BAC clones.
Main Methods:
- The NIG_MoG database visualizes single-nucleotide polymorphisms and short insertions/deletions.
- Genome data is presented in comparison to C57BL/6J, derived from M. m. domesticus.
- In silico screening of BAC clones containing genomic DNA from MSM/Ms and C57BL/6N is supported.
Main Results:
- NIG_MoG offers intuitive visualization of genome divergence between Mus musculus subspecies.
- The database allows for easy identification of genetic variations.
- Users can efficiently screen for relevant BAC clones.
Conclusions:
- NIG_MoG is a valuable tool for researchers, particularly wet-lab biologists.
- It aids in understanding intersubspecific genome divergence in mice.
- The database supports studies on gene function and regulation using mouse genome polymorphisms and BAC clones.
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