GenoWatch: a disease gene mining browser for association study.

@article{citeulike:2804080, abstract = {A human gene association study often involves several genomic markers such as single nucleotide polymorphisms (SNPs) or short tandem repeat polymorphisms, and many statistically significant markers may be identified during the study. GenoWatch can efficiently extract up-to-date information about multiple markers and their associated genes in batch mode from many relevant biological databases in real-time. The comprehensive gene information retrieved includes gene ontology, function, pathway, disease, related articles in PubMed and so on. Subsequent SNP functional impact analysis and primer design of a target gene for re-sequencing can also be done in a few clicks. The presentation of results has been carefully designed to be as intuitive as possible to all users. The GenoWatch is available at the website http://genepipe.ngc.sinica.edu.tw/genowatch.}, address = {National Genotyping Center (NGC) and Institute of Biomedical Sciences (IBMS), Academia Sinica, Taipei, Taiwan 11529, R.O.C.}, author = {Chen, Yan-Hau H. and Liu, Chuan-Kun K. and Chang, Shu-Chuan C. and Lin, Yi-Jung J. and Tsai, Ming-Fang F. and Chen, Yuan-Tsong T. and Yao, Adam }, citeulike-article-id = {2804080}, issn = {1362-4962}, journal = {Nucleic acids research}, keywords = {association}, month = {April}, posted-at = {2008-05-16 05:29:14}, priority = {2}, title = {GenoWatch: a disease gene mining browser for association study.}, url = {http://view.ncbi.nlm.nih.gov/pubmed/18440974}, year = {2008} }

TY - JOUR ID - citeulike:2804080 L3 - citeulike-article-id:2804080 TI - GenoWatch: a disease gene mining browser for association study. JF - Nucleic acids research AD - National Genotyping Center (NGC) and Institute of Biomedical Sciences (IBMS), Academia Sinica, Taipei, Taiwan 11529, R.O.C. SN - 1362-4962 N2 - A human gene association study often involves several genomic markers such as single nucleotide polymorphisms (SNPs) or short tandem repeat polymorphisms, and many statistically significant markers may be identified during the study. GenoWatch can efficiently extract up-to-date information about multiple markers and their associated genes in batch mode from many relevant biological databases in real-time. The comprehensive gene information retrieved includes gene ontology, function, pathway, disease, related articles in PubMed and so on. Subsequent SNP functional impact analysis and primer design of a target gene for re-sequencing can also be done in a few clicks. The presentation of results has been carefully designed to be as intuitive as possible to all users. The GenoWatch is available at the website http://genepipe.ngc.sinica.edu.tw/genowatch. KW - association AU - Chen, Yan-Hau AU - Liu, Chuan-Kun AU - Chang, Shu-Chuan AU - Lin, Yi-Jung AU - Tsai, Ming-Fang AU - Chen, Yuan-Tsong AU - Yao, Adam PY - 2008/04/25/ UR - http://view.ncbi.nlm.nih.gov/pubmed/18440974 ER -