schließen

Dr. med. univ. Dr. rer. nat. Gundula Povysil, MSc

{{ dict().Publications }}

{{ typ[0].TYP }}

{{ dict().Lectures }}

{{ typ[0].TYP }}

{{ dict().ResearchProjects }}

{{ typ[0].TYP }}

{{ dict().Scs }}

{{ typ[0].TYP }}

{{ dict().Innovations }}

{{ typ[0].TYP }}

Ausbildung

  • 10/2017: Graduation from the Johannes Kepler University Linz with the degree Dr. rer. nat. (PhD)
    • Thesis: Analyzing NGS Data with Machine Learning - From IBD Segments to Copy Number Variations
  • 2013 - 2017: PhD Studies Bioinformatics, Johannes Kepler University Linz
  • 02/2013: Graduation from the Johannes Kepler University Linz with the degree MSc.
    • Thesis: IBD Mapping of Autism Microarray Data - Beyond Linkage and Association Mapping
  • 2010 - 2013: Master Studies Bioinformatics, Johannes Kepler University Linz
  • 07/2010: Graduation from the Medical University Vienna with the degree Dr. med. univ. (MD)
  • 2008 - 2009: Diploma theses at the Institute of Medical Genetics, Vienna (Proportion of SPRED1 mutation carriers in NF1-negative children with café-au-lait spots)
  • 2004 - 2010: Medical studies, Medical University Vienna
  • 06/2004: Matura (high school graduation) at BG/BRG Khevenhüller with distinction
  • 1996 - 2004: Secondary School: BG/BRG Khevenhüller, Linz
  • 1992 - 1996: Elementary School: Volksschule Römerberg, Linz

Forschungsthemen

  • Machine Learning
  • Deep Learning
  • Genetics
  • Sequence Analysis
  • Copy Number Variations
  • Disease Associations
  • Population Genetics
  • Identity by Descent (IBD) Detection

Software

panelcn.mops R package: CNV detection tool for targeted NGS panel data.

For more information see http://bioinf.jku.at/software/panelcnmops/

Papers

  • Povysil G., Tzika A., Vogt J., Haunschmid V., Messiaen L., Zschocke J., Klambauer G., Hochreiter S. and Wimmer K. (2017). panelcn.MOPS: Copy number detection in targeted NGS panel data for clinical diagnostics. Human Mutation 38 (7): 889-897. doi:10.1002/humu.23237 Abstract
  • Clevert D.-A., Unterthiner T., Povysil G and Hochreiter S. (2017). Rectified Factor Networks for Biclustering of Omics Data. Bioinformatics33 (14): i59-i66. doi:10.1093/bioinformatics/btx226 Abstract
  • Povysil G, Hochreiter S. (2016). IBD Sharing between Africans, Neandertals, and Denisovans.Genome Biology and Evolution 8 (12): 3406-3416. doi:10.1093/gbe/evw234 Abstract
  • Povysil G, Hochreiter S. (2014). Sharing of very short IBD segments between humans, Neandertals, and Denisovans. bioRxiv.

Vorträge

  • ÖGH 2016, Vienna, Austria: panelcn.MOPS: CNV detection in targeted panel sequencing data for diagnostic use
  • ASHG 2015, Baltimore, MD, USA: IBD sharing in the 1000 Genomes Project Phase 3 data reveals relationships from Neandertals to present day families

Poster

  • NIPS Workshop on ML in Computational Biology 2017, Long Beach, CA, USA: HapRFN: Rectified Factor Networks for identifying short IBD segments
  • WiML 2017, Long Beach, CA, USA: panelcn.MOPS - a mixture of Poissons model for copy number detection
  • ESHG 2017, Copenhagen, Denmark: panelcn.MOPS: CNV detection in targeted NGS panel data for clinical diagnostics
  • WiML 2016, Barcelona, Spain: HapRFN: a deep learning method for identifying short IBD segments
  • ASHG 2016, Vancouver, Canada: panelcn.MOPS: CNV detection in targeted panel sequencing data for diagnostic use
  • ASHG 2015, Baltimore, MD, USA: panelcn.MOPS reaches clinical standards as a CNV detection tool for targeted panel sequencing data
  • SMBE 2015, Vienna, Austria: Early Interbreeding between Ancestors of Humans, Neandertals, and Denisovans within Africa
  • ASHG 2014, San Diego, CA, USA: Population specific patterns of novel haplotype groups at the PAH locus
  • ASHG 2013, Boston, MA, USA: IBD Mapping of Autism Microarray Data
  • ASHG 2012, San Francisco, CA, USA: Detection of identity by descent based on rare variants
  • HGV 2012, Shanghai, China: Identifying IBD tracts that are tagged by rare variants
  • ISMB 2012, Long Beach, CA, USA: Comparison of IBD detection methods with a focus on rare variants

Lehrerfahrungen

  • Summer semester 2015 - 2016: Exercises in Theoretical Concepts of Machine Learning & Exercises in Machine Learning: Unsupervised Techniques
  • Summer semester 2014 and 2017: Special Topics on Bioinformatics: Population genetics
  • Summer semester 2013: Exercises in Theoretical Bioinformatics and Machine Learning
  • Winter semester 2012/13 - 2017/18: Exercises in Sequence Analysis and Phylogenetics