Green, R. E., J. Krause, A. W. Briggs, T. Maricic, U. Stenzel, M. Kircher, N. Patterson, H. Li, W. Zhai, M. H.-Y. Fritz, N. F. Hansen, E. Y. Durand, A.-S. Malaspinas, J. D. Jensen, T. Marques-Bonet, C. Alkan, K. Prüfer, M. Meyer, H. A. Burbano, J. M. Good, R. Schultz, A. Aximu-Petri, A. Butthoff, B. Höber, B. Höffner, M. Siegemund, A. Weihmann, C. Nusbaum, E. S. Lander, C. Russ, N. Novod, J. Affourtit, M. Egholm, C. Verna, P. Rudan, D. Brajkovic, Z. Kucan, I. Gusic, V. B. Doronichev, L. V. Golovanova, C. Lalueza-Fox, M. Rasilla, J. Fortea, A. Rosas, R. W. Schmitz, P. L. F. Johnson, E. E. Eichler, D. Falush, E. Birney, J. C. Mullikin, M. Slatkin, R. Nielsen, J. Kelso, M. Lachmann, D. Reich and S. Pääbo: A Draft Sequence of the Neandertal Genome. In: Science 328, 5979, 710-722 (2010).
doi: 10.1126/science.1188021
Turnbaugh, P.J., C. Quince, J.J. Faith, A. McHardy, T. Yatsunenko, F. Niazi, J. Affourtit, M. Egholm, B. Henrissat, R. Knight and J.I. Gordon: Organismal, genetic, and transcriptional variation in the deeply sequenced gut microbiomes of identical twins. In: Proceedings of the National Academy of Sciences of the United States of America 107, 16, 7503-7508 (2010).
doi: 10.1073/pnas.1002355107
localid: C1257539004AF554-84BAAA3033FDEA9BC12577ED005AA274-mchardy2010ogt
Krause, J., R. E. Green, A. W. Briggs, U. Stenzel, K. Prüfer, T. Maricic, M. Kichner, J. F. Kelso, D. Reich, J. C. Mullikin, M. Egholm and S. Pääbo: Insights from Sequencing the Neanderthal Genome. In: American Journal of Physical 138, S48 (Supplement), 170-170 (2009).
Green, R. E., A.-S. Malaspinas, J. Krause, A. W. Briggs, P. L. F. Johnson, C. Uhler, M. Meyer, J. M. Good, T. Maricic, U. Stenzel, K. Prüfer, M. Siebauer, H. A. Burbano, M. T. Ronan, J. M. Rothberg, M. Egholm, P. Rudan, D. Brajkovic, Z. Kucan, I. Gusic, M. Wikström, L. Laakkonen, J. F. Kelso, M. Slatkin and S. Pääbo: A Complete Neandertal Mitochondrial Genome Sequence Determined by High-Throughput Sequencing. In: Cell 134, 3, 416-426 (2008).
doi: 10.1016/j.cell.2008.06.021
Green, R. E., J. Krause, S. E. Ptak, A. W. Briggs, M. T. Ronan, J. F. Simons, L. Du, M. Egholm, J. M. Rothberg, M. Paunovic and S. Pääbo: Analysis of one million base pairs of Neanderthal DNA. In: Nature 444, 330-336 (2006).
doi: 10.1038/nature05336
Stiller, M., R. E. Green, M. T. Ronan, J. F. Simons, L. Du, M. Egholm, J. M. Rothberg, S. G. Keats, N. D. Ovodov, E. E. Antipina, G. F. Baryshnikov, Y. V. Kuzmin, A. A. Vasilevski, G. E. Wuenschell, J. Termini, M. Hofreiter, V. R. Jänicke-Després, S. Pääbo and W. He: Patterns of nucleotide misincorporations during enzymatic amplification and direct large-scale sequencing of ancient DNA. In: PNAS 103, 37, 13578-13584 (2006).
Thomas, R. K., E. Nickerson, J. F. Simons, P. A. Jänne, T. Tengs, Y. Yuza, L. A. Garraway, T. Laframboise, J. C. Lee, K. Shah, K. O'Neill, H. Sasaki, N. Lindeman, K.-K. Wong, A. M. Borras, E. J. Gutmann, K. H. Dragnev, R. Debiasi, T.-H. Chen, K. A. Glatt, H. Greulich, B. Desany, C. K. Lubeski, W. Brockman, P. Alvarez, S. K. Hutchison, J. H. Leamon, M. T. Ronan, G. S. Turenchalk, M. Egholm, W. R. Sellers, J. M. Rothberg and M. Meyerson: Sensitive mutation detection in heterogeneous cancer specimens by massively parallel picoliter reactor sequencing. In: Nature Medicine 12, 7, 852-855 (2006).
Thomas, R. K., H. Greulich, Y. Yuza, J. C. Lee, T. Tengs, W. Feng, T.-H. Chen, E. Nickerson, J. Simons, M. Egholm, J. M. Rothberg, W. R. Sellers and M. L. Meyerson: Detection of oncogenic mutations in the EGFR gene in lung adenocarcinoma with differential sensitivity to EGFR tyrosine kinase inhibitors. In: Cold Spring Harbor Symposia on Quantitative Biology 70, 73-81 (2005).
doi: 10.1101/sqb.2005.70.056
The Max Planck Society does not take any responsibility for the content of this export.