9th Annual Biomarkers Congress
Clinical Genomics & Informatics Europe
Sheraton Hotel & Spa
Rua Latino Coelho No 1
Lisbon, Portugal
http://www.clinicalgenomicsinformatics.com/
Clinical Genomics & Informatics Europe
Cambridge Healthtech Institute 
http://www.clinicalgenomicsinformatics.com/
Sheraton Hotel & Spa
Rua Latino Coelho No 1
Lisbon
Portugal

Schedule of Presentations:

Wednesday, December 4, 2013
07:30:00 Registration and Morning Coffee
08:30:00 Chairperson’s Opening Remarks Hans-Hilger Ropers
08:40:00 New Sequencing Techniques: Why They are Indispensable for Health Care, and What We Can Do to Speed Up Their Clinical Implementation Hans-Hilger Ropers
09:10:00 External Quality Assessment for NGS David E. Barton
09:40:00 Targeted Next-Generation Sequencing Can Replace Sanger Sequencing in Clinical Diagnostics Jan D. H. Jongbloed
10:10:00 Coffee Break in the Exhibit Hall with Poster Viewing
10:40:00 Chairperson’s Remarks Gholson J. Lyon
10:45:00 Comparing Exome vs. Genome Sequencing for Genetic Component of Diseases Han G. Brunner
11:15:00 Comparing Clinical v. Whole Exome Sequencing for Monogenic Diseases and Undiagnosed Patients
11:45:00 Sponsored Presentation (Sponsorship Opportunity Available)
12:15:00 Luncheon Presentation (Sponsorship Opportunity Available) or Lunch on Your Own
13:15:00 Session Break
14:05:00 Increasing Accuracy for Exome and Whole Genome Sequencing Gholson J. Lyon
14:35:00 Changing the Clinical Genetic Testing Paradigm: Reducing Cost and Increasing Utility
15:05:00 Experiences from our Integrated Genomics Clinic; Rapid Identification and Clinical Reporting of Causative Mutations through WGS and WES Elizabeth Worthey
15:35:00 Sponsored Presentation (Sponsorship Opportunity Available)
16:05:00 Refreshment Break in the Exhibit Hall with Poster Viewing
16:45:00 Exome Sequencing in Complex Disease: Data Quality and Clinical Heterogeneity
17:15:00 Panel Discussion with Day’s Speakers
17:45:00 Welcome Reception in the Exhibit Hall with Poster Viewing
19:15:00 Close of Day
Thursday, December 5, 2013
08:00:00 Morning Coffee
08:30:00 Chairperson’s Opening Remarks
08:35:00 Strategies for Disease-Gene Identification in Exome Sequencing Peter Robinson
09:05:00 The Post-WGS Cancer Genome: Alphabet Soup, Syllabus or Cyclopaedia?
09:35:00 Sponsored Presentation (Sponsorship Opportunity Available)
10:05:00 Coffee Break in the Exhibit Hall with Poster Viewing
10:45:00 Sponsored Presentation (Sponsorship Opportunity Available)
11:15:00 Integrated Exome Sequencing and Copy Number Analysis of Pancreatic Cancer Reveals a HER2-Amplified Subtype
11:30:00 Conference Registration
11:45:00 From Genome Annotation to Genome Medicine Timothy Hubbard
11:45:00 From Genome Annotation to Genome Medicine Timothy Hubbard
12:35:00 Enjoy Lunch on Your Own
12:35:00 Close of Conference
14:00:00 Chairperson’s Opening Remarks
14:05:00 Annotate-it and eXtasy: Interpretation and Prioritization of Single-Nucleotide Variation in Clinical Genomics
14:35:00 TAG (Tumor Analysis in Galaxy): A Web Server Application for the Detection of Somatic Mutations in the Absence of Associated Healthy Control
15:05:00 Harnessing e-Science Central for NGS Simon Woodman
15:15:00 Interpreting Genomic Variation in the Research and Clinical Context Using OmicsOffice on the Spotfire Analytics Platform Eduardo Gonzalez-Couto
15:50:00 Sponsored Presentation (Sponsorship Opportunity Available)
16:05:00 Refreshment Break in the Exhibit Hall with Poster Viewing
16:50:00 Big Science & Biomedicine at Petascale
17:20:00 Sequenza – A Bayesian Analytical Framework to Provide Comprehensive Characterization of Tumor Samples Based on Exome Sequencing Zoltan Szallasi
17:50:00 EVA-Suite (Exome Variation Analyzer): A User-Friendly Web Solution for Annotating, Filtering and Prioritizing Candidate Variants in Medical Genomics Hélène Dauchel
18:20:00 Close of Day
Friday, December 6, 2013
08:00:00 Morning Coffee
08:30:00 Chairperson’s Opening Remarks
08:35:00 Clinical Genome Architecture Circuitry and Next-Generation Cancer Drug Targets Dimitrios H Roukos
09:05:00 Big Data in Drug Discovery – Challenges and Perspectives Philip Groth
09:35:00 Sponsored Presentation (Sponsorship Opportunity Available)
10:05:00 Coffee Break in the Exhibit Hall with Poster Viewing
10:45:00 The Ethical Introduction of Genome-Based Information and Technologies into Public Health Heidi Carmen Howard
11:15:00 Challenges of Translation of Next-Generation Sequencing to Clinical Practice Angel Carracedo
11:45:00 How the Electronic Healthcare Record Can Facilitate Translational and Integrative Medicine
12:15:00 The Ethical Dimensions of Data Sharing and the Maze of Identifiability Anne Cambon-Thomsen
12:45:00 Luncheon Presentation (Sponsorship Opportunity Available) or Lunch on Your Own
13:15:00 Session Break
14:00:00 Chairperson’s Opening Remarks
14:35:00 RNA-Seq and Microarray Gene Expression Vie for Superiority within a Comprehensive Study Design Weida Tong
15:05:00 Multi-Platform and Cross-Methodological Reproducibility of Transcriptome Profiling by RNA-Seq in the ABRF Next-Generation Sequencing Study (ABRF-NGS) Christopher Mason
15:35:00 Functional Dysregulation in Inflammatory Diseases
16:05:00 Close of Conference
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