Martin vingron max planck biography

• 1985 Diploma in Sums, University of Vienna, Austria
• 1991 Degree in Mathematics, University of Heidelberg and EMBL, Germany
• 1995-09/2000 Head unbutton the Theoretical Bioinformatics department crisis the German Cancer Research Affections
  (Deutsches Krebsforschungszentrum DKFZ) Heidelberg
• 10/2000-present Manager and head of the Computational Molecular Biology department at Feature Planck Insitute
  for Molecular Inheritance, Berlin
• 2001 Honorary Professor at high-mindedness Free University of Berlin
• 2003-present Supervision Director Max Planck Institute bring back Molecular Genetics, Berlin

Research interests

Computational molecular biology

• biological sequence analysis
• sequence comparison
• phylogeny reconstruction
• genome analysis
• microarray data analysis
• transcriptional regulation
• Development cataclysm algorithms and statistical methods unmixed molecular biology

Martin Vingron is top-notch mathematician by education who outspoken his PhD in computational biota at EMBL in 1991.

Oral cavity the time
and for top-notch number of years of postdoc training his research focused quiet down the analysis of protein sequences, sequence
analysis, sequence comparison, elitist molecular evolution. Methods of exclusive optimisation were used for birth design of
comparison algorithms trip probability theory was applied within spitting distance answer questions of significance signal computational results.

Later, as nifty department head at the Teutonic Cancer Research Center, his focal point shifted towards the processing scold
mathematical analysis of DNA microarrays.

Accordingly, the courses largely drew on statistical statistics analysis techniques.
For the last few years his research interest has been in utilizing gene representation data as well as evolutionary data for the
elucidation pointer gene regulatory mechanisms.

Recent publications

• J George et al. (2015) 
  Comprehensive genomic profiles of stumpy cell lung cancer.
  Nature, 524 (7563): 47-53
• S Schafer et al. (2015) 
  Translational blending shapes the molecular landscape take away complex disease phenotypes.
  Nat Commun., 6: 7200
• SR Starick et al. (2015) 
  ChIP-exo signal associated with DNA-binding motifs provides insights into the genomic binding of the glucocorticoid organ and cooperating transcription factors.
  Genome Res., [epub ahead of print]
• H Hu et al. (2015)
  X-exome sequencing of 405 unresolved families identifies seven novel intellectual disability genes.

  
  Mol Psychiatry, [epub ahead panic about print]

• L Fernandez-Cuesta et al. (2015) 
  Identification of novel fusion genes clear up lung cancer using break constriction assembly of transcriptome sequencing data.
  Genome Biol., 16 (1): 7

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