Bibliography
- et al., 2012
-
, . G. P. C., Abecasis, G. R., Auton, A., Brooks, L. D., DePristo, M. A.,
Durbin, R. M., Handsaker, R. E., Kang, H. M., Marth, G. T., and McVean, G. A.
(2012).
An integrated map of genetic variation from 1,092 human genomes.
Nature, 491(7422):56-65. - Bamford et al., 2004
-
Bamford, S., Dawson, E., Forbes, S., Clements, J., Pettett, R., Dogan, A.,
Flanagan, A., Teague, J., Futreal, P. A., Stratton, M. R., and Wooster, R.
(2004).
The cosmic (catalogue of somatic mutations in cancer) database and website.
Br J Cancer, 91(2):355-358. - Choi et al., 2009
-
Choi, M., Scholl, U. I., Ji, W., Liu, T., Tikhonova, I. R., Zumbo, P., Nayir,
A., Bakkaloglu, A., Özen, S., Sanjad, S., Nelson-Williams, C., Farhi,
A., Mane, S., and Lifton, R. P. (2009).
Genetic diagnosis by whole exome capture and massively parallel DNA sequencing.
Proc Natl Acad Sci U S A, 106(45):19096-19101. - Heap et al., 2010
-
Heap, G. A., Yang, J. H. M., Downes, K., Healy, B. C., Hunt, K. A., Bockett,
N., Franke, L., Dubois, P. C., Mein, C. A., Dobson, R. J., Albert, T. J.,
Rodesch, M. J., Clayton, D. G., Todd, J. A., van Heel, D. A., and Plagnol,
V. (2010).
Genome-wide analysis of allelic expression imbalance in human primary cells by high-throughput transcriptome resequencing.
Hum Mol Genet, 19(1):122-134. - Martin and Wang, 2011
-
Martin, J. A. and Wang, Z. (2011).
Next-generation transcriptome assembly.
Nat Rev Genet, 12(10):671-682. - Ng et al., 2009
-
Ng, S. B., Turner, E. H., Robertson, P. D., Flygare, S. D., Bigham, A. W., Lee,
C., Shaffer, T., Wong, M., Bhattacharjee, A., Eichler, E. E., Bamshad, M.,
Nickerson, D. A., and Shendure, J. (2009).
Targeted capture and massively parallel sequencing of 12 human exomes.
Nature, 461(7261):272-276. - Wang et al., 2009
-
Wang, Z., Gerstein, M., and Snyder, M. (2009).
RNA-Seq: a revolutionary tool for transcriptomics.
Nat Rev Genet, 10(1):57-63.
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