Biology Reference
In-Depth Information
(looking for mutations that can explain sudden death [54, 55]), is likely to become
more widespread.
References
1. Miller, R.D., Phillips, M.S., Jo, I., Donaldson, M.A., Studebaker, J.F., Addleman, N. et al .
(2005) High-density single-nucleotide polymorphism maps of the human genome. Genomics ,
86 , 117 - 126.
2. Sachidanandam, R., Weissman, D., Schmidt, S.C., Kakol, J.M., Stein, L.D., Marth, G. et al .
(2001) A map of human genome sequence variation containing 1.42 million single nucleotide
polymorphisms. Nature , 409 , 928 - 933.
3. Thorisson, G.A. and Stein, L.D. (2003) The SNP consortium website: past, present and future.
Nucleic Acids Research , 31 , 124 -127.
4. Brookes, A.J. (1999) The essence of SNPs. Gene , 234 , 177 - 186.
5. Lander, E.S., Linton, L.M., Birren, B., Nusbaum, C., Zody, M.C., Baldwin, J. et al . (2001)
Initial sequencing and analysis of the human genome. Nature , 409 , 860 - 921.
6. Venter, J.C., Adams, M.D., Myers, E.W., Li, P.W., Mural, R.J., Sutton, G.G. et al . (2001) The
sequence of the human genome. Science , 291 , 1304 - 1351.
7. Gibbs, R.A., Belmont, J.W., Hardenbol, P., Willis, T.D., Yu, F.L., Yang, H.M. et al . (2003)
The International HapMap Project. Nature , 426 , 789 - 796.
8. Frazer, K.A., Ballinger, D.G., Cox, D.R., Hinds, D.A., Stuve, L.L., Gibbs, R.A. et al .
(2007) A second generation human haplotype map of over 3.1 million SNPs. Nature , 449 ,
U851 -U853.
9. Musumeci, L., Arthur, J.W., Cheung, F.S.G., Hoque, A., Lippman, S. and Reichardt, J.K.V.
(2010) Single Nucleotide Differences (SNDs) in the dbSNP database may lead to errors in
genotyping and haplotyping studies. Human Mutation , 31 , 67 - 73.
10. Sherry,
S.T.,
Ward,
M.H.,
Kholodov, M.,
Baker,
J.,
Phan,
L.,
Smigielski, E.M.
et al .
(2001)
dbSNP:
the
NCBI
database
of
genetic
variation.
Nucleic
Acids
Research , 29 ,
308 - 311.
11. Ahn, S.M., Kim, T.H., Lee, S., Kim, D., Ghang, H., Kim, D.S. et al . (2009) The first Korean
genome sequence and analysis: full genome sequencing for a socio-ethnic group. Genome
Research , 19 , 1622 -1629.
12. Bentley, D.R., Balasubramanian, S., Swerdlow, H.P., Smith, G.P., Milton, J., Brown, C.G. et al .
(2008) Accurate whole human genome sequencing using reversible terminator chemistry.
Nature , 456 , 53 - 59.
13. Levy, S., Sutton, G., Ng, P.C., Feuk, L., Halpern, A.L., Walenz, B.P. et al . (2007) The diploid
genome sequence of an individual human. PLoS Biology , 5 , 2113 -2144.
14. Schuster, S.C., Miller, W., Ratan, A., Tomsho, L.P., Giardine, B., Kasson, L.R. et al . (2010)
Complete Khoisan and Bantu genomes from southern Africa. Nature , 463 , 943 - 947.
15. Wang, J., Wang, W., Li, R.Q., Li, Y.R., Tian, G., Goodman, L. et al . (2008) The diploid
genome sequence of an Asian individual. Nature , 456 , U60 - U61.
16. Wheeler, D.A., Srinivasan, M., Egholm, M., Shen, Y., Chen, L., McGuire, A. et al . (2008)
The complete genome of an individual by massively parallel DNA sequencing. Nature , 452 ,
U872 -U875.
17. Gill, P. (2001) An assessment of the utility of single nucleotide polymorphisms (SNPs) for
forensic purposes. International Journal of Legal Medicine , 114 , 204 - 210.
18. Krawczak, M. (2001) Forensic evaluation of Y-STR haplotype matches: a comment. Forensic
Science International , 118 , 114 - 115.
19. Danna, K. and Nathans, D. (1971) Studies of Sv40 DNA. 1. Specific cleavage of Simian virus
40 DNA by restriction endonuclease of Hemophilus influenzae. Proceedings of the National
Academy of Sciences of the United States of America , 68 , 2913 -2291.
20. Denaro, M., Blanc, H., Johnson, M.J., Chen, K.H., Wilmsen, E., Cavallisforza, L.L. et al .
(1981) Ethnic variation in Hpa-I endonuclease cleavage patterns of human mitochondrial-DNA.
Search WWH ::




Custom Search