Complete MHC Haplotype Sequencing for Common Disease Gene Mapping

The future systematic mapping of variants that confer susceptibility to common diseases requires the construction of a fully informative polymorphism map. Ideally, every base pair of the genome would be sequenced in many individuals. Here, we report 4.75 Mb of contiguous sequence for each of two com...

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Päätekijät: Stewart, C. Andrew, Horton, Roger, Allcock, Richard J.N., Ashurst, Jennifer L., Atrazhev, Alexey M., Coggill, Penny, Dunham, Ian, Forbes, Simon, Halls, Karen, Howson, Joanna M.M., Humphray, Sean J., Hunt, Sarah, Mungall, Andrew J., Osoegawa, Kazutoyo, Palmer, Sophie, Roberts, Anne N., Rogers, Jane, Sims, Sarah, Wang, Yu, Wilming, Laurens G., Elliott, John F., de Jong, Pieter J., Sawcer, Stephen, Todd, John A., Trowsdale, John, Beck, Stephan
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Cold Spring Harbor Laboratory Press 2004
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Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC419796/
https://ncbi.nlm.nih.gov/pubmed/15140828
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1101/gr.2188104
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