JSNP: a database of common gene variations in the Japanese population

JSNP is a repository of Japanese Single Nucleotide Polymorphism (SNP) data, begun in 2000 and developed through the Prime Minister's Millennium Project. The aim of this undertaking is to identify and collate up to 150 000 SNPs from the Japanese population, located in genes or in adjacent regions that might influence the coding sequence of the genes. The project has been carried out by a collaboration between the Human Genome Center (HGC) in the Institute of Medical Science (IMS) at the University of Tokyo and the Japan Science and Technology Corporation (JST). JSNP serves as both a storage site for the Japanese SNPs obtained from the ongoing project and as a facility for public dissemination to allow researchers access to high quality SNP data. A primary motivation of the project is the construction of a basic data set to identify relationships between polymorphisms and common diseases or the reaction to drugs. As such, emphasis has been placed on the identification of SNPs that lie in candidate regions which may affect phenotype but which would not necessarily directly cause disease. Unrestricted access to JSNP and any associated files is available at http://snp.ims.u-tokyo.ac.jp/.

[1]  C. Burge Chapter 8 – Modeling dependencies in pre-mRNA splicing signals , 1998 .

[2]  Hideaki Sugawara,et al.  DNA Data Bank of Japan (DDBJ) in collaboration with mass sequencing teams , 2000, Nucleic Acids Res..

[3]  G D Schuler,et al.  Electronic PCR: bridging the gap between genome mapping and genome sequencing. , 1998, Trends in biotechnology.

[4]  Gregory D. Schuler,et al.  Database resources of the National Center for Biotechnology Information: update , 2004, Nucleic acids research.

[5]  Simon Kasif,et al.  Computational methods in molecular biology , 1998 .

[6]  Donna R. Maglott,et al.  RefSeq and LocusLink: NCBI gene-centered resources , 2001, Nucleic Acids Res..

[7]  Elizabeth M. Smigielski,et al.  dbSNP: the NCBI database of genetic variation , 2001, Nucleic Acids Res..

[8]  D. Mccormick Sequence the Human Genome , 1986, Bio/Technology.

[9]  P Sham,et al.  A SNP resource for human chromosome 22: extracting dense clusters of SNPs from the genomic sequence. , 2001, Genome research.

[10]  Ian Korf,et al.  MaskerAid : a performance enhancement to RepeatMasker , 2000, Bioinform..

[11]  S Rozen,et al.  Primer3 on the WWW for general users and for biologist programmers. , 2000, Methods in molecular biology.

[12]  P. Green,et al.  Consed: a graphical tool for sequence finishing. , 1998, Genome research.

[13]  Yan P. Yuan,et al.  HGBASE: a database of SNPs and other variations in and around human genes , 2000, Nucleic Acids Res..

[14]  P. Bucher,et al.  A cSNP map and database for human chromosome 21. , 2001, Genome research.

[15]  Evelyn Camon,et al.  The EMBL Nucleotide Sequence Database , 2004, Nucleic acids research.

[16]  K. Sirotkin,et al.  dbSNP-database for single nucleotide polymorphisms and other classes of minor genetic variation. , 1999, Genome research.

[17]  David J. States,et al.  Identification of protein coding regions by database similarity search , 1993, Nature Genetics.

[18]  References , 1971 .

[19]  D. Nickerson,et al.  PolyPhred: automating the detection and genotyping of single nucleotide substitutions using fluorescence-based resequencing. , 1997, Nucleic acids research.