The phenotype and genotype experiment object model (PaGE‐OM): a robust data structure for information related to DNA variation
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Toshio Kojima | Akihiko Konagaya | Debasis Dash | Kimitoshi Naito | Hideaki Sugawara | Martin Senger | Hiroshi Mizushima | Ituro Inoue | Gudmundur A. Thorisson | Juha Muilu | Gudmundur A Thorisson | Anthony J Brookes | Haseena Rajeevan | Yasumasa Shigemoto | Mark Woon | Matthew W. Darlison | A. Konagaya | H. Sugawara | M. Woon | Albert Vernon Smith | A. Brookes | M. Senger | D. Dash | H. Lehvaslaiho | I. Inoue | T. Kojima | D. Fredman | J. Muilu | Albert V Smith | David Fredman | H. Mizushima | Yasumasa Shigemoto | T. Oroguchi | Takeshi Tomiki | Atsuhiro Mukaiyama | Masako Kuroda | Haseena Rajeevan | K. Naito | Takeshi Tomiki | Heikki Lehvaslaiho | Takashige Oroguchi | Atsuhiro Mukaiyama | Masako Kuroda | Matthew W Darlison | H. Rajeevan | A. Smith | Mark Woon | David Fredman | Martin Senger
[1] Elizabeth M. Smigielski,et al. dbSNP: the NCBI database of genetic variation , 2001, Nucleic Acids Res..
[2] R. Cotton. Recommendations of the 2006 Human Variome Project meeting , 2007, Nature Genetics.
[3] P. Donnelly,et al. Replicating genotype–phenotype associations , 2007, Nature.
[4] B. Knoppers,et al. Population Genomics: The Public Population Project in Genomics (P3G): a proof of concept? , 2008, European Journal of Human Genetics.
[5] Sarah Lewis,et al. Genetic epidemiology and public health: hope, hype, and future prospects , 2005, The Lancet.
[6] Kei-Hoi Cheung,et al. ALFRED: the ALelle FREquency Database. Update , 2003, Nucleic Acids Res..
[7] Gudmundur A. Thorisson,et al. Genotype–phenotype databases: challenges and solutions for the post-genomic era , 2009, Nature Reviews Genetics.
[8] Debasis Dash,et al. The Indian Genome Variation database (IGVdb): a project overview , 2005, Human Genetics.
[9] Jason E. Stewart,et al. Design and implementation of microarray gene expression markup language (MAGE-ML) , 2002, Genome Biology.
[10] Russ B Altman,et al. PharmGKB: a logical home for knowledge relating genotype to drug response phenotype , 2007, Nature Genetics.
[11] R B Altman,et al. An XML‐based interchange format for genotype–phenotype data , 2008, Human mutation.
[12] D. Fredman,et al. HGVbase: a curated resource describing human DNA variation and phenotype relationships , 2004, Nucleic Acids Res..
[13] Toshihiro Tanaka. The International HapMap Project , 2003, Nature.
[14] Debasis Dash,et al. HGVbaseG2P: a central genetic association database , 2008, Nucleic Acids Res..
[15] Gudmundur A. Thorisson,et al. The International HapMap Project Web site. , 2005, Genome research.
[16] Chris F. Taylor,et al. The MGED Ontology: a resource for semantics-based description of microarray experiments , 2006, Bioinform..
[17] C. Sander,et al. The HUPO PSI's Molecular Interaction format—a community standard for the representation of protein interaction data , 2004, Nature Biotechnology.
[18] E. Mardis. The impact of next-generation sequencing technology on genetics. , 2008, Trends in genetics : TIG.
[19] Yusuke Nakamura,et al. JSNP: a database of common gene variations in the Japanese population , 2002, Nucleic Acids Res..
[20] B. C. Mishra,et al. Consortium IGVThe Indian Genome Variation database (IGVdb): a project overview. Hum Genet 118:1-11 , 2005 .
[21] Nigel W. Hardy,et al. The Functional Genomics Experiment model (FuGE): an extensible framework for standards in functional genomics , 2007, Nature Biotechnology.