최소 단어 이상 선택하여야 합니다.
최대 10 단어까지만 선택 가능합니다.
다음과 같은 기능을 한번의 로그인으로 사용 할 수 있습니다.
NTIS 바로가기Genomics & informatics, v.4 no.1, 2006년, pp.45 - 47
Kang Hyo-Jin (National Genome Information Center, Korea Research Institute of Bioscience and Biotechnology) , Hong Tae-Hui (National Genome Information Center, Korea Research Institute of Bioscience and Biotechnology) , Chung Won-Hyong (National Genome Information Center, Korea Research Institute of Bioscience and Biotechnology) , Kim Young-Uk (National Genome Information Center, Korea Research Institute of Bioscience and Biotechnology) , Jung Jin-Hee (National Genome Information Center, Korea Research Institute of Bioscience and Biotechnology) , Hwang So-Hyun (National Genome Information Center, Korea Research Institute of Bioscience and Biotechnology) , Han A-Reum (National Genome Information Center, Korea Research Institute of Bioscience and Biotechnology) , Kim Young-Joo (National Genome Information Center, Korea Research Institute of Bioscience and Biotechnology)
D2GSNP is a web-based server for the selection of single nucleotide polymorph isms (SNPs) within genes related to human diseases. The D2GSNP is based on a relational database created by downloading and parsing OMIM, GAD, and dbSNP, and merging it with positional information of UCSC Golden Path. Tota...
* AI 자동 식별 결과로 적합하지 않은 문장이 있을 수 있으니, 이용에 유의하시기 바랍니다.
Day, C. P. (2005). Genetic studies to identify hepatic fibrosis genes and SNPs in human populations. Methods Mol. Med. 117, 315-331
Gray, I. C., Campbell, D. A., and Spurr, N. K. (2000). Single nucleotide polymorph isms as tools in human genetics. Hum Mol. Gene. 9, 2403-2408
Hacia, J. G., Fan, J. B., Ryder, O., Jin, L., Edgemon, K., Ghandour, G., Mayer, R. A., Sun, B., Hsie, L., Robbins, C. M. et al. (1999). Determination of ancestral alleles for human single-nucleotide polymorph isms using highdensity oligonucleotide arrays. Nat. Genet. 22, 164-167
Hamosh, A., Scott, A.F., Amberger, J., Bocchini, C., Valle, D., and McKusick, V.A. (2002). Online Mendelian Inheritance in Man (OMIM), a knowledgebase of human genes and genetic disorders. Nucleic Acids Res. 30, 52-55
Hirschhorn, J.N. (2005). Genetic approaches to studying common diseases and complex traits. Pediatr. Res. 57 (5 Pt 2), 74R-77R
Lopez-Bigas, N. and Ouzounis, C.A. (2004). Genome-wide identification of genes likely to be involved in human genetic disease. Nucleic Acids Res. 32, 3108-3114
Marnellos, G. (2003). High-throughput SNP analysis for genetic association studies. Curr. Opin. Drug Discov. . Devel. 6, 317-321
Mooser, V., Waterworth, D.M., Isenhour, T., and Middleton, L. (2003). Cardiovascular pharmacogenetics in the SNP era. J. Thromb. Haemost. 1, 1398-1402
Perez-Iratxeta, C., Bork, P., and Andrade, M.A. (2002). Association of genes to genetically inherited diseases using data mining. Nature Genet. 31, 316-319
Sherry, S.T., Ward, M.H., Kholodov, M., Baker, J., Phan, L., Smigielski, E.M., and Sirotkin, K. (2001). dbSNP: the NCBI database of genetic variation. Nucleic Acids Res. 29, 308-311
Tiffin, N., Kelso, J.F., Powell, A.R., Pan, H., Bajic, V.B., and Hide, W.A. (2005). Integration of text- and data-mining using ontologies successfully selects disease gene candidates. Nucleic Acids Res. 33, 1544-1552
Becker, K.G., Barnes, K.C., Bright, T.J., and Wang, S.A. (2004). The Genetic Association Database. http://geneticassociationdb.nih.gov/
Kent, W.J., Sugnet, C.W. Furey, T.S., Roskin, K.M., Pringle, T.H., Zahler, A.M., and Haussler, D. (2002). The human genome browser at UCSC. http://genome.ucsc.edu/
McKusick-Nathans Institute for Genetic Medicine, Johns Hopkins University (Baltimore,MD) and National Center for Biotechnology Information, National Library of Medicine (Bethesda, MD). (2000). Online Mendelian Inheritance in Man, OMIM (TM). http://www.ncbi.nlm.nih.gov/omim/
Sherry, S.T., Ward, M.H., Kholodov, M., Baker, J., Phan, L., Smigielski, E.M, and Sirotkin, K. (2001). dbSNP: the NCBI database of genetic variation. http://www.ncbi.nlm.nih.gov/SNP/
*원문 PDF 파일 및 링크정보가 존재하지 않을 경우 KISTI DDS 시스템에서 제공하는 원문복사서비스를 사용할 수 있습니다.
※ AI-Helper는 부적절한 답변을 할 수 있습니다.