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.

#17046#>