Accurate and Fast Detection of Complex and Nested Structural Variations Using Long-read Technologies.
Talk, Functional Genomics: Towards Precision Medicine 2017, Doha, Qatar
Slides are available on request
Talks and presentations
See a map of all the places I've given a talk!
Accurate and Fast Detection of Complex and Nested Structural Variations Using Long-read Technologies.
Talk, ASHG 2017, Orlando, USA
Slides are available here: Slides
Structural Variation Characterization Across the Human Genome and Populations.
Talk, GRC/GiaB Workshop ASHG 2017, Orlando, USA
Slides are available here: Slides
Accurate detection of complex structural variations using PacBio.
Keynote Talk, PacBio Bioinformatics Workshop, Baltimore, USA
Mapping of NGS reads.
Talk, Johns Hopkins University, Baltimore, USA
Identification and interpretation of structural variations from yeast to human cancers using short and long reads.
Talk, Baylor College of Medicine, Houston, USA
Accurate and fast detection of complex and nested structural variations using long read technologies.
Conference Talk, Biological Data Science, Cold Spring Harbour, USA
Accurate detection and analysis of structural variations in healthy and cancerous human genomes.
Talk, University College London, London, UK
Accurate detection of SVs using short and long read sequencing.
Talk, Max Planck Institute for Evolutionary Biology, Ploen, Germany
Accurate and fast detection of complex and nested structural variations using long read technologies.
Talk, University of Lausanne, Lausanne, Switzerland
Accurate detection of SVs using high throughput sequencing.
Talk, Cibiv-Max F. Perutz Laboratories, Vienna, Austria
Workshop on Structural Variations.
Organizer Workshop, Festival of Genomics, Boston, USA
Identification of structural variations from long reads.
Talk, Johns Hopkins Univiersity, Baltimore, USA
Identification and interpretation of structural variations from yeast to human cancers using short and long reads.
Talk, University of Massachusetts, Worcester, USA
Structural Variation detection using long reads.
Conference Talk, Genome in a bottle workshop, Stanford, USA
Accurate Assessment of Structural Variations.
Talk, Cold Spring Harbor Laboratory, Cold Spring Harbor, USA
Methods for improved SV detection and interpretation.
Conference Talk, Genome in a bottle workshop, Gaithersburg, USA
NextGenMap: How to accurately map 150,000 reads per second and why should we care
Talk, Cold Spring Harbor Laboratory, Cold Spring Harbor, USA
Impact of highly polymorphic regions on HTS analysis
Talk, University College London, London, UK
NextGenMap: Fast and accurate read mapping independent of evolutionary distance.
Conference Talk, MASAMB 2013, London, UK
NextGenMap: Fast and accurate read mapping independent of evolutionary distance
Talk, Max Planck Institute for Evolutionary Biology, Ploen, Germany
MASon: Million Alignments In Seconds - A Platform Independent Pairwise Sequence Alignment Library for Next Generation Sequencing Data.
Conference Talk, BIOINFORMATICS 2012, Vilamoura, Portugal
Comprehensive Evaluation of NGS Mapping Programs
Talk, Austrian Agency for Health and Food Safety (AGES), Vienna, Austria
Identifying wrongly mapped reads via majority vote of several scoring schemata.
Conference Talk, European Science Foundation - COST action: StatSeq meeting on RNA-Seq, Vienna, Austria
Whole Genome Sequencing: Possibilities, Perspectives and Problems for the Analysis
Talk, Research Institute of Molecular Pathology (IMP), Vienna, Austria
NextGenMap: Using high throughput hardware for high throughput sequencing
Talk, Research Institute of Molecular Pathology (IMP), Vienna, Austria
From CPU to GPU: An Application in bioinformatics
Talk, TU Munich, Department of Testing, Munich, Germany