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Prenatal Molecular Diagnostics Europe

 
  February 07, 2014  
     
 
Lisbon Marriott Hotel, Lisbon, Portugal
12-13 May 2014


This conference aims to take an in-depth look at the current trends and guidelines in Europe for prenatal molecular diagnostics, while providing perspectives on how this rapidly changing field is likely to develop in Europe over the next several years. In addition to the technical issues, there are a number of other factors, including geographic differences, coverage of diagnostic tests from one country to another, challenges of clinical implementation of new procedures and the increased need for genetic counseling perspectives, that need to be understood in order to forecast how this field is likely to develop in Europe.

Agenda: 

ADVANCES AND CHALLENGES FOR PRENATAL MOLECULAR DIAGNOSTICS IN EUROPE 

  • Current Status, Issues and Challenges for Molecular Analysis of Invasively Obtained Prenatal Samples
  • NIPT Advances, Limitations and Future Directions
  • Change of Mind: Advances in Technology Call for Personalized Prenatal Testing

CYTOGENETICS AND CHROMOSOMAL MICROARRAYS 

  • Prenatal Arrays in the UK – Proposals for a National Approach
  • From Conventional to Molecular Karyotyping in a Diagnostic Laboratory – Challenges and Dilemmas
  • Prenatal Whole Genome SNP Array Diagnosis as a First-Line Test: Nature and Prevalence of Abnormal Results in Phenotypically Normal and Abnormal Fetuses
  • Data and Analysis using Array CGH for Prenatal Diagnostics

SEQUENCING OF CELL-FREE DNA 

  • A New Era in Prenatal Care: The Implementation of Non-Invasive Prenatal Testing (NIPT) in Switzerland
  • Introduction of Non-Invasive Prenatal Testing (NIPT) in the Netherlands
  • Ethical Issues and Considerations for the Implementation of Cell-Free DNA Sequencing
  • Epigenetic Strategies for NIPD: The Power of the Fetal Methylome
  • Development and Use of the WISECONDOR Programme for the Analysis of NIPT Data
  • Contingent cfDNA Screening with Additional Serum Markers – A Highly Cost-Effective Strategy
  • Non-invasive Cell-free DNA-based Prenatal Detection of Microdeletions using Single Nucleotide Polymorphism Targeted Sequencing

ISOLATION AND ANALYSIS OF FETAL CELLS FROM MATERNAL BLOOD 

  • Genetic Analysis of Trophoblastic Cells Isolated by ISET for Non-Invasive Prenatal Diagnosis
  • Progress in the Isolation and Identification of Fetal Cells from Maternal Blood
  • Isolation and Characterization of Individual Circulating Fetal Cells for Non-Invasive Prenatal Diagnosis
 
 
Organized by: Cambridge Healthtech Institute
Invited Speakers: For speaker information, click here.
 
Deadline for Abstracts: ---
 
Registration: Register now
E-mail: kwaterman@healthtech.com
 
   
 
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