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
- NGS_users_meeting_program_2010.pdf (356.58 kb)
Programme NGS user meeting

