Publikationen von A.-K. Emde

H. Hu, S. A. Haas, J. Chelly, H. Van Esch, M. Raynaud, A. P. M. de Brouwer, S. Weinert, G. Froyen, S. G. M. Frints, F. Laumonnier, T. Zemojtel, M. I. Love, H. Richard, A.-K. Emde, M. Bienek, C. Jensen, M. Hambrock, U. Fischer, C. Langnick, M. Feldkamp, W. Wissink-Lindhout, N. Lebrun, L. Castelnau, J. Rucci, R. Montjean, O. Dorseuil, P. Billuart, T. Stuhlmann, M. Shaw, M. A. Corbett, A. Gardner, S. Willis-Owen, C. Tan, K. L. Friend, S. Belet, K. E. P. van Roozendaal, M. Jimenez-Pocquet, M.-P. Moizard, N. Ronce, R. Sun, S. O'Keeffe, R. Chenna, A. van Bömmel, J. Göke, A. Hackett, M. Field, L. Christie, J. Boyle, E. Haan, J. Nelson, G. Turner, G. Baynam, G. Gillessen-Kaesbach, U. Müller, D. Steinberger, B. Budny, M. Badura-Stronka, A. Latos-Bieleńska, L. B. Ousager, P. Wieacker, G. Rodríguez Criado, M.-L. Bondeson, G. Annerén, A. Dufke, M. Cohen, L. Van Maldergem, C. Vincent-Delorme, B. Echenne, B. Simon-Bouy, T. Kleefstra, M. Willemsen, J.-P. Fryns, K. Devriendt, R. Ullmann, M. Vingron, K. Wrogemann, T. F. Wienker, A. Tzschach, H. van Bokhoven, J. Gecz, T. J. Jentsch, W. Chen, H.-H. Ropers, and V. M. Kalscheuer, "X-exome sequencing of 405 unresolved families identifies seven novel intellectual disability genes," Molecular Psychiatry 21 (1), 133-148 (2016).

Ruping Sun, Michael Love, Tomas Zemojtel, Anne-Katrin Emde, Ho-Ryun Chung, Martin Vingron, and Stefan Haas, "Breakpointer: using local mapping artifacts to support sequence breakpoint discovery from single-end reads," Bioinformatics 28 (7), 1024-1025 (2012).

A. K. Emde, M. Grunert, D. Weese, K. Reinert, and S. R. Sperling, "MicroRazerS: rapid alignment of small RNA reads," Bioinformatics 26 (1), 123-124 (2010).

Tobias Rausch, Anne-Katrin Emde, David Weese, Andreas Döring, Cedric Notredame, and Knut Reinert, "Segment-based multiple sequence alignment," Bioinformatics 24(16): (16), i187-i192 (2008).

Witold E. Wolski, Malcolm Farrow, Anne-Katrin Emde, Hans Lehrach, Maciej Lalowski, and Knut Reinert, "Analytical model of peptide mass cluster centres with applications," Proteome Science 4, 18-18 (2006).

Anne-Katrin Emde, Next-generation sequencing algorithms: from read mapping to variant detection, PhD Thesis, Berlin, 2013.