Print this page

Programme NGS User meeting, July 6, 2010

   
9.00 Registration
   
9.30 Plenary session I
9.30 NGS around the world; where are NGS laboratories, and what do they do?
  James Hadfield, Genomics Core Facility, Cambridge Research Institute, Cambridge (UK)
9.45 NGS at Max Planck Institute; organization and collaboration
  Bernd Timmermann, Max Planck Institute for Molecular Genetics, Berlin (GE)
   
11.00 Coffee break
   
11.30 Parallel Session A
  1. Bioinformatic solutions, Chair: Marc van Driel
  a. PRICAT: a web-tool for the analysis of plant ChIP-seq experiments
  Marlous Hoogstraat
  b. Pattern finding in ChIP-seq data using CATCH (Clustering and Alignment of ChIP profiles)
  Fiona Nielsen
  c. Integrating genome assemblies with MAIA Motivation
  Jurgen Nijkamp
  d. SSPACE: a new scaffolding tool
  Walter Pirovano
   
  2. Experimental workflow, Chair: Matthew Hestand
  a. Large scale exome resequencing on the SOLiD platform
  Christian Gilissen
  b. Monitoring strain diversity in metagenomics data using meta-MLST SNP profiling
  Victor de Jager
  c. Detecting alterations in genome structure from paired tags
  Victor Guryev
  d. Advanced Nucleic Acid Fractionation for Next Generation Sequencing Sample Preparation
  Hannes Arnold
   
13.00 Lunch
   
14.00 Parallel Session B
  3. Clinical applications, Chair: Joris Veltman
  a. Multiplexing in a diagnostic setting
  Magdalena Harakalova
  b. Unprecedented resolution for the detection of inherited and de novo structural variation by mate-pair sequencing of a family trio
  Wigard Kloosterman
  c. BRCA1 screening using 454 sequencing
  Koos Kranenburg
  d. Design and validation of a NGS approach for hereditary blindness in diagnostics
  Kornelia Neveling
   
  4. Fundamental research applications, Chair: Edwin Cuppen
  a. Globin reduction in blood samples for next generation sequencing gene expression studies
  A. Mastrokolias
  b. Pol II chromatin immunoprecipitation and sequencing (ChIP-seq) as a measure of transcription rate
  Michal Mokry
  c. De Novo Genome Sequencing and Annotation of the Basal Flatworm Macrostomum Lignano
  Daniil Simanov
  d. 4C-seq: capturing the 3D-organization of the mammalian genome
  Elzo de Wit
   
15.15 Tea break
   
15.45 Plenary session II
15.45 Understanding the Genome with NGS; notes on genomics and bioinformatics
  Melissa Fullwood, Duke-NUS Graduate Medical School/Genome Institute of Singapore, Singapore
   
17.00 Drinks
   
18.30 End program
   

Programme in PDF

Back to homepage NGS users meeting