Genetic Analysis Workshop 17 mini-exome simulation

BMC Proceedings - 2011
Laura Almasy1, Thomas D. Dyer1, Juan M. Peralta2, Jack W. Kent1, Jac Charlesworth3, Joanne E. Curran1, John Blangero1
1Department of Genetics, Texas Biomedical Research Institute, 7620 NW Loop 410, San Antonio, TX, 78245, USA
2Centro de Investigación en Biología Molecular y Celular, Universidad de Costa Rica, San José, Costa Rica
3Menzies Research Institute, 17 Liverpool St (Private Bag 23), Hobart, Tasmania, 7001, Australia

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Tài liệu tham khảo

The 1000 Genomes Project Consortium: A map of human genome variation from population-scale sequencing. Nature. 2010, 467: 1061-1073. 10.1038/nature09534.

McKenna A, Hanna M, Banks E, Sivachenko A, Cibulskis K, Kernytsky A, Garimella K, Altshuler D, Gabriel S, Daly M, et al: The Genome Analysis Toolkit: a MapReduce framework for analyzing next-generation DNA sequencing data. Genome Res. 2010, 20: 1297-1303. 10.1101/gr.107524.110.

Terwilliger JD, Speer M, Ott J: Chromosome-based method for rapid computer simulation in human genetic linkage analysis. Genet Epidemiol. 1993, 10: 217-224. 10.1002/gepi.1370100402.

MacCluer JW, Blangero J, Dyer TD, Speer MC: GAW10: simulated family data for a common oligogenic disease with quantitative risk factors. Genet Epidemiol. 1997, 14: 737-742. 10.1002/(SICI)1098-2272(1997)14:6<737::AID-GEPI29>3.0.CO;2-Q.

Almasy L, Terwilliger JD, Nielsen D, Dyer TD, Zaykin D, Blangero J: GAW12: simulated genome scan, sequence, and family data for a common disease. Genet Epidemiol. 2001, 21 (suppl 2): S332-S338.

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