Program

DEFINITIVE PROGRAM including Posters (in PDF format: NGS2009-PROGRAM)

DEFINITIVE BOOK of ABSTRACTS (in PDF format: NGS2009-BOOK)

THURSDAY 1st OCTOBER

8h30 - 9h30: Registration

9h30 - 9h45: Presentation (M. Pérez-Enciso)

9h45 - 10h30: Inaugural speech (Chair: D. Torrents)

10h30 - 11h00: General Genomics

[ 11h00 - 11h30 Coffee break ]

11h30 - 13h00 Technology session (Chair: M. Pérez-Enciso)

  • 11h30 - J. Knight (Roche): Sequencing Solutions for Small and Large Genomes.
  • 12h00 - M.T. Ross (Illumina): Sequencing Human Genomes using Genome analyzer.
  • 12h30 - R. Dixon (Applied Biosystems): Introducing BioScopeT for SOLID System Data Analysis

[ 13h00 - 15h00 LUNCH AND POSTER VIEWING ]

15h00 -16h30: General Genomics (Chair: J. García)

[ 16h30 - 17h00 Coffee break ]

17h00 - 18h45: Computational Challenges (Chair: )

[ 19h00 - GROUP PICTURE ]

[ 19h15 - WELCOME COCKTAIL AND POSTER VIEWING]


FRIDAY 2nd OCTOBER

9h30 - 11h00 - Population Genomics (I) (Chair: A. Navarro)

[ 11h00 - 11h30 Coffee break ]

11h30 - 13h00 - Population Genomics (II) (Chair: S. E. Ramos-Onsins / D. De Lorenzo)

[ 13h00 - 15h00 LUNCH AND POSTER VIEWING ]

15h00 - 16h30 - Functional Genomics (I) (Chair: J. Bertranpetit)

[ 11h00 - 11h30 Coffee break ]

17h00 - 18h30 - General and Functional Genomics (II) (Chair: M. Bink)

[ 20h30 - CONGRESS DINNER ]


SATURDAY 3rd OCTOBER

09h30 - 10h45 - MetaGenomics (Chair: Kua C. S.)

[ 10h45 - 11h15 Coffee break ]

11h15 - 12h15 - EpiGenomics (Chair: J. Cruz Cigudosa)

12h15 - 13h15 - Round Table (Chair: A. Navarro)

[ 13h15 - FAREWELL C0CKTAIL ]


POSTER LIST
(Only shown the Corresponding Author)
Please place your poster in the panel with assigned number

General Genomics

P1. Garcia-Mas, J. Towards the Whole Sequence of the Melon Genome.
P2. Bergero, R. Using 454 Sequencing of ESTs for Linkage Analyses in a Dioecious Plant Species.
P3. Kua, CS. Using a 'Framework Species' Concept for Ecological and Evolutionary Studies in Comparative Genomics.
P4. Esteve, A. Partial Short-Read Resequencing of a Highly Inbred Iberian Pig.
P5. Lin, Y-C. Genome Sequence of the Recombinant Protein Production Host Pichia pastoris.
P6. Tobes, R. Mutant HIV Minority Variants Detected by Ultradeep Sequencing do Not Condition Virological Failure in Patients Starting ARV Therapy Including Low Genetic Barrier Drugs.

Bioinformatics and Population Genomics

P7. Amaral, A.J. Finding Selection Footprints in the Swine Genome Using Massive Parallel Sequencing.
P8. Balzer, S. Novel Tools and Methods for Exploring Pyrosequencing Data Including Quality Assessment and Simulation.
P9. Bink, M. StatSeq : Statistical Challenges on the 1000 Genome Sequences in Plants (EU COST Action TD0801).
P10. Megens, H.-J. Genome-Wide Assessment of Nucleotide Diversity and Signatures of Selection in Chicken Using Massive Parallel Sequencing.
P11. Tobes, R. Cloud Computing and NGS: Massively Parallel Computing for Massively Parallel Sequencing.
P12. Barbadilla, A. Genome Browser of Genetic Diversity in Drosophila.
P13. Toro, M.A. Including Dominance Effects in Genomic Selection.
P14. Unterländer, M. Using Next Generation Sequencing on Ancient DNA – Preamplified Via a New Muliplex Approach – to Detect Migration and Population Structure.

Transcriptomics and Metagenomics

P15. Cancio, I. Pyrosequencing of Non-Model Sentinel Species for Gene Transcription Profiling Studies in Environmental Pollution Monitoring.
P16. Gosalbes M.J. High-Throughput Sequencing Technologies Applied to Human Gut Microbiota Research and Genomics of Pathogens.
P17. Piferrer, F. Analysis of the Gonadal Transcriptome During Sex Determination, Sex Differentiation and Gonadal Maturation in the Sea Bass (Dicentrarchus labrax) and Turbot (Scophthalmus maximus) by 454 Sequencing and Two Specific Oligo-Based Microarrays.
P18. Schönfeld, B. I. K. Rhopalodia gibba and its Spheroid Body - Sequencing Endosymbiosis.
P19. Stuglik, M. Investigating Molecular Basis of Response to Selection in Bank Vole with Next Generation Sequencing.
P20. Haase, B. Selection of Cancer-Related Gene Exons for Targeted Resequencing with a Flexible and Fully Automated Microarray Platform.