1. Bailey, J. A., Gu, Z., Clark, R. A., et al. (2002) Recent segmental duplications in the human genome. Science 297, 1003-1007.

2. Cheung, J., Estivill, X., Khaja, R., et al. (2003) Genome-wide detection of segmental duplications and potential assembly errors in the human genome sequence. Genome Biol. 4, R25.

3. Cheung, J., Wilson, M. D., Zhang, J., et al. (2003) Recent segmental and gene duplications in the mouse genome. Genome Biol. 4, R47.

4. Bailey, J. A., Church, D. M., Ventura, M., Rocchi, M., and Eichler, E. E. (2004) Analysis of segmental duplications and genome assembly in the mouse. Genome Res. 14, 789-801.

5. Tuzun, E., Bailey, J. A., and Eichler, E. E. (2004) Recent segmental duplications in the working draft assembly of the brown Norway rat. Genome Res. 14, 493-506.

6. Lupski, J. R. (1998) Genomic disorders: structural features of the genome can lead to DNA rearrangements and human disease traits. Trends Genet. 14, 417-422.

7. Stankiewicz, P. and Lupski, J. R. (2002) Genome architecture, rearrangements and genomic disorders. Trends Genet. 18, 74-82.

8. Eichler, E. E. (2001) Recent duplication, domain accretion and the dynamic mutation of the human genome. Trends Genet. 17, 661-669.

9. Ji, Y., Eichler, E. E., Schwartz, S., and Nicholls, R. D. (2000) Structure of chromosomal duplicons and their role in mediating human genomic disorders. Genome Res. 10, 597-610.

10. Iafrate, A. J., Feuk, L., Rivera, M. N., et al. (2004) Detection of large-scale variation in the human genome. Nat. Genet. 36, 949-951.

11. Armengol, L., Pujana, M. A., Cheung, J., Scherer, S. W., and Estivill, X. (2003) Enrichment of segmental duplications in regions of breaks of synteny between the human and mouse genomes suggest their involvement in evolutionary rearrangements. Hum. Mol. Genet. 12, 2201-2208.

12. Bailey, J. A., Baertsch, R., Kent, W. J., Haussler, D., and Eichler, E. E. (2004) Hotspots of mammalian chromosomal evolution. Genome Biol. 5, R23.

13. Ohno, S. (1970) Evolution by Gene Duplication. Springer, New York, NY.

14. Buiting, K., Korner, C., Ulrich, B., Wahle, E., and Horsthemke, B. (1999) The human gene for the poly(A)-specific ribonuclease (PARN) maps to 16p13 and has a truncated copy in the Prader-Willi/Angelman syndrome region on 15q11^q13. Cytogenet. Cell Genet. 87, 125-131.

15. Altschul, S. F., Gish, W., Miller, W., Myers, E. W., and Lipman, D. J. (1990) Basic local alignment search tool. J. Mol. Biol. 215, 403-410.

16. Zhang, Z., Schwartz, S., Wagner, L., and Miller, W. (2000) A greedy algorithm for aligning DNA sequences. J. Comput. Biol. 7, 203-214.

17. Prince, V. E. and Pickett, F. B. (2002) Splitting pairs: the diverging fates of duplicated genes. Nat. Rev. Genet. 3, 827-837.

18. Ashburner, M., Ball, C. A., Blake, J. A., et al. (2000) Gene ontology: tool for the unification of biology. Nat. Genet. 25, 25-29.

0 0

Post a comment