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2020 – today
- 2020
[j8]Davide Bolognini
, Ashley D. Sanders, Jan O. Korbel, Alberto Magi, Vladimir Benes, Tobias Rausch:
VISOR: a versatile haplotype-aware structural variant simulator for short- and long-read sequencing. Bioinform. 36(4): 1267-1269 (2020)
2010 – 2019
- 2019
- [j7]Tobias Rausch, Markus Hsi-Yang Fritz, Jan O. Korbel, Vladimir Benes:
Alfred: interactive multi-sample BAM alignment statistics, feature counting and feature annotation for long- and short-read sequencing. Bioinform. 35(14): 2489-2491 (2019) - 2018
- [j6]Nikola Tom, Ondrej Tom, Jitka Malcikova, Sarka Pavlova, Blanka Kubesova, Tobias Rausch, Miroslav Kolarík, Vladimir Benes, Vojtech Bystrý, Sarka Pospisilova:
ToTem: a tool for variant calling pipeline optimization. BMC Bioinform. 19(1): 243:1-243:9 (2018) - 2012
- [j5]Tobias Rausch, Thomas Zichner, Andreas Schlattl, Adrian M. Stütz, Vladimir Benes, Jan O. Korbel:
DELLY: structural variant discovery by integrated paired-end and split-read analysis. Bioinform. 28(18): 333-339 (2012) - 2010
- [b1]Tobias Rausch:
Dissecting multiple sequence alignment methods: the analysis, design and development of generic multiple sequence alignment components in SeqAn. Free University of Berlin, 2010
2000 – 2009
- 2009
- [j4]Tobias Rausch, Sergey Koren, Gennady Denisov, David Weese, Anne-Katrin Emde, Andreas Döring, Knut Reinert:
A consistency-based consensus algorithm for de novo and reference-guided sequence assembly of short reads. Bioinform. 25(9): 1118-1124 (2009) - [c3]Robert Strobl, Thomas Müllner, Tobias Rausch:
Web-Based Process Portals: Powering Business Process Management within Large Organisations. CEC 2009: 312-316 - 2008
- [j3]Andreas Döring, David Weese, Tobias Rausch, Knut Reinert:
SeqAn An efficient, generic C++ library for sequence analysis. BMC Bioinform. 9 (2008) - [j2]Tobias Rausch, Anne-Katrin Emde, Knut Reinert:
Robust consensus computation. BMC Bioinform. 9(S-10) (2008) - [j1]Tobias Rausch, Alun Thomas, Nicola J. Camp, Lisa A. Cannon-Albright, Julio C. Facelli:
A parallel genetic algorithm to discover patterns in genetic markers that indicate predisposition to multifactorial disease. Comput. Biol. Medicine 38(7): 826-836 (2008) - [c2]Tobias Rausch, Anne-Katrin Emde, David Weese, Andreas Döring, Cédric Notredame, Knut Reinert:
Segment-based multiple sequence alignment. ECCB 2008: 187-192 - [c1]Marcel H. Schulz, David Weese, Tobias Rausch, Andreas Döring, Knut Reinert, Martin Vingron:
Fast and Adaptive Variable Order Markov Chain Construction. WABI 2008: 306-317
Coauthor Index
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