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High-performance information extraction with AliBaba.

P. Palaga, L. Nguyen, U. Leser, and J. Hakenberg. EDBT, volume 360 of ACM International Conference Proceeding Series, page 1140-1143. ACM, (2009)

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Dr. phil. Christian Jörg University of Stuttgart

Fabian Jörg University of Stuttgart

Jörg Desel

Das ist InformatikJ. Desel (Eds.) Springer, (2001)

Das ist InformatikJ. Desel (Eds.) Springer, (2001)Hilfreiche Hilfe Methode, Implementierung und Evaluation eines Verfahrens zur Adaption an das prozedurale WissenD. Iglezakis. Kath. Universität Eichstätt-Ingolstadt, Aachen, (2007)Hilfreiche Hilfe Methode, Implementierung und Evaluation eines Verfahrens zur Adaption an das prozedurale WissenD. Iglezakis. Kath. Universität Eichstätt-Ingolstadt, Aachen, (2007)

Jörg Förstner University of Stuttgart

Jörg Roth University of Stuttgart

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A high-throughput analysis pipeline for large next generation DNA sequencing studies.Z. Albertyn, J. Hakenberg, H. Bian, H. Niu, and J. Cai. BIBM, page 1. IEEE Computer Society, (2012)Mining relations from the biomedical literature.J. Hakenberg. Humboldt University of Berlin, (2009)Literature Mining Solutions for Life Science Research.J. Hakenberg, G. Nenadic, D. Rebholz-Schuhmann, and J. Kim. Adv. Bioinformatics, (2013)Towards Effective Sentence Simplification for Automatic Processing of Biomedical TextS. Jonnalagadda, L. Tari, J. Hakenberg, C. Baral, and G. Gonzalez. CoRR, (2010)Towards Effective Sentence Simplification for Automatic Processing of Biomedical Text.S. Jonnalagadda, L. Tari, J. Hakenberg, C. Baral, and G. Gonzalez. HLT-NAACL (Short Papers), page 177-180. The Association for Computational Linguistics, (2009)Word Sense Disambiguation in Biomedical Applications.T. Schiemann, U. Leser, and J. Hakenberg. Information Retrieval in Biomedicine, IGI Global, (2009)Collecting a Large Corpus from all of Medline.J. Hakenberg, U. Leser, H. Kirsch, and D. Rebholz-Schuhmann. SMBM, volume 177 of CEUR Workshop Proceedings, CEUR-WS.org, (2006)Integrating 400 million variants from 80, 000 human samples with extensive annotations: towards a knowledge base to analyze disease cohorts.J. Hakenberg, W. Cheng, P. Thomas, Y. Wang, A. Uzilov, and R. Chen. BMC Bioinformatics, (2016)Systematic feature evaluation for gene name recognition.J. Hakenberg, S. Bickel, C. Plake, U. Brefeld, H. Zahn, L. Faulstich, U. Leser, and T. Scheffer. BMC Bioinformatics, (2005)DIVAS: a centralized genetic variant repository representing 150 000 individuals from multiple disease cohorts.W. Cheng, J. Hakenberg, S. Li, and R. Chen. Bioinformatics, 32 (1): 151-153 (2016)