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ROCR: visualizing classifier performance in R

Bioinformatics, 2005-10, Vol.21 (20), p.3940-3941

2005

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BiQ Analyzer: visualization and quality control for DNA methylation data from bisulfite sequencing

Bioinformatics, 2005-11, Vol.21 (21), p.4067-4068

2005

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Importance of bioinformatics in personalised medicine

Bundesgesundheitsblatt, Gesundheitsforschung, Gesundheitsschutz, 2013-11, Vol.56 (11), p.1489-1494

Lengauer, T

2013

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Sarcoidosis is associated with a truncating splice site mutation in BTNL2

Nature genetics, 2005-04, Vol.37 (4), p.357-364

2005

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Algorithms—ESA '93: First Annual European Symposium Bad Honnef, Germany September 30–October 2, 1993 Proceedings

Lengauer, Thomas

1993

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STACS 90: 7th Annual Symposium on Theoretical Aspects of Computer Science Rouen, France, February 22–24, 1990 Proceedings

1990

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P0895 : Comparison of three sequencing methods commonly used in hepatitis C virus resistance analysis: population-based vs. clonal vs. ultra deep sequencing

Journal of hepatology, 2015-04, Vol.62, p.S679-S679

2015

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Computational methods for the design of effective therapies against drug resistant HIV strains

Bioinformatics, 2005-11, Vol.21 (21), p.3943-3950

2005

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Engineering support vector machine kernels that recognize translation initiation sites

Bioinformatics, 2000-09, Vol.16 (9), p.799-807

2000

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P1106 UPDATED geno2pheno[HCV] WEB SERVICE PERFORMS RESISTANCE ANALYSIS BASED ON NS3, NS5A AND NS5B SEQUENCE DATA

Journal of hepatology, 2014-04, Vol.60 (1), p.S446-S446

2014

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Full genome ultra-deep pyrosequencing associates G-to-A hypermutation of the hepatitis B virus genome with the natural progression of hepatitis B

Journal of viral hepatitis, 2013-12, Vol.20 (12), p.882-889

2013

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BinPacker: Packing-Based De Novo Transcriptome Assembly from RNA-seq Data

PLoS computational biology, 2016-02, Vol.12 (2), p.e1004772-e1004772

2016

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Hepatitis C Virus Screening Project of Patients on Current Anti-HCV Therapy

Journal of hepatology, 2016, Vol.64 (2), p.S402-S402

2016

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Prediction of response to antiretroviral therapy by human experts and by the EuResist data‐driven expert system (the EVE study)

HIV medicine, 2011-04, Vol.12 (4), p.211-218

2011

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Predicting protein ligand binding sites by combining evolutionary sequence conservation and 3D structure

PLoS computational biology, 2009-12, Vol.5 (12), p.e1000585

2009

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406 FULL GENOME ULTRA-DEEP PYROSEQUENCING INDICATES AN IMPORTANT ROLE OF HYPERMUTATION IN THE NATURAL PROGRESSION OF CHRONIC HEPATITIS B

Journal of hepatology, 2013-04, Vol.58, p.S167-S167

2013

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Mtreemix: a software package for learning and using mixture models of mutagenetic trees

Bioinformatics, 2005-05, Vol.21 (9), p.2106-2107

2005

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Bioinformatics--from genomes to drugs

Lengauer, T. (Thomas)

2002

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499 FULL GENOME ULTRA-DEEP PYROSEQUENCING IDENTIFIES GG-TO-GA HYPERMUTATION AS NOVEL PREDICTOR FOR TREATMENT RESPONSE TO PEGYLATED INTERFERON ALFA-2A IN HBEAG-NEGATIVE CHRONIC HEPATITIS B

Journal of hepatology, 2012-04, Vol.56, p.S197-S197

2012

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1204 THE PEPSI PROJECT: HCV RESISTANCE SCREENING AND PREDICTION OF PI-CONTAINING THERAPY OUTCOME

Journal of hepatology, 2013-04, Vol.58, p.S489-S490

2013

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356 IDENTIFICATION OF HBV DUAL INFECTION USING DIRECT SEQUENCING DATA

Journal of hepatology, 2011-03, Vol.54, p.S143-S143

2011

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Estimating cancer survival and clinical outcome based on genetic tumor progression scores

Bioinformatics, 2005-05, Vol.21 (10), p.2438-2446

2005

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MRFalign: protein homology detection through alignment of Markov random fields

PLoS computational biology, 2014-03, Vol.10 (3), p.e1003500-e1003500

2014

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Simple consensus procedures are effective and sufficient in secondary structure prediction

Protein engineering, 2003-07, Vol.16 (7), p.459-462

2003

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Genotypic coreceptor analysis

European journal of medical research, 2007-10, Vol.12 (9), p.453-462

2007

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ROCR: visualizing classifier performance in R

BiQ Analyzer: visualization and quality control for DNA methylation data from bisulfite sequencing

Importance of bioinformatics in personalised medicine

Sarcoidosis is associated with a truncating splice site mutation in BTNL2

Algorithms—ESA '93: First Annual European Symposium Bad Honnef, Germany September 30–October 2, 1993 Proceedings

STACS 90: 7th Annual Symposium on Theoretical Aspects of Computer Science Rouen, France, February 22–24, 1990 Proceedings

P0895 : Comparison of three sequencing methods commonly used in hepatitis C virus resistance analysis: population-based vs. clonal vs. ultra deep sequencing

Computational methods for the design of effective therapies against drug resistant HIV strains

Engineering support vector machine kernels that recognize translation initiation sites

P1106 UPDATED geno2pheno[HCV] WEB SERVICE PERFORMS RESISTANCE ANALYSIS BASED ON NS3, NS5A AND NS5B SEQUENCE DATA

Full genome ultra-deep pyrosequencing associates G-to-A hypermutation of the hepatitis B virus genome with the natural progression of hepatitis B

BinPacker: Packing-Based De Novo Transcriptome Assembly from RNA-seq Data

Hepatitis C Virus Screening Project of Patients on Current Anti-HCV Therapy

Prediction of response to antiretroviral therapy by human experts and by the EuResist data‐driven expert system (the EVE study)

Predicting protein ligand binding sites by combining evolutionary sequence conservation and 3D structure

406 FULL GENOME ULTRA-DEEP PYROSEQUENCING INDICATES AN IMPORTANT ROLE OF HYPERMUTATION IN THE NATURAL PROGRESSION OF CHRONIC HEPATITIS B

Mtreemix: a software package for learning and using mixture models of mutagenetic trees

Bioinformatics--from genomes to drugs

499 FULL GENOME ULTRA-DEEP PYROSEQUENCING IDENTIFIES GG-TO-GA HYPERMUTATION AS NOVEL PREDICTOR FOR TREATMENT RESPONSE TO PEGYLATED INTERFERON ALFA-2A IN HBEAG-NEGATIVE CHRONIC HEPATITIS B

1204 THE PEPSI PROJECT: HCV RESISTANCE SCREENING AND PREDICTION OF PI-CONTAINING THERAPY OUTCOME

356 IDENTIFICATION OF HBV DUAL INFECTION USING DIRECT SEQUENCING DATA

Estimating cancer survival and clinical outcome based on genetic tumor progression scores

MRFalign: protein homology detection through alignment of Markov random fields

Simple consensus procedures are effective and sufficient in secondary structure prediction

Genotypic coreceptor analysis

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