Informed consent for whole-genome sequencing studies in the clinical setting. Proposed recommendations on essential content and process.

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From Guideline Database

This database contains updated guidelines, policies and recommendations on genomic research and practice, as provided by professional organizations, federal advisory groups, expert panels and policy groups.

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• Informed consent for whole-genome sequencing studies in the clinical setting. Proposed recommendations on essential content and process.  
  Published 2013
• Current issues in medically assisted reproduction and genetics in Europe: research, clinical practice, ethics, legal issues and policy. European Society of Human Genetics and European Society of Human Reproduction and Embryology.  
  Published 2013
• Whole-genome sequencing in newborn screening? A statement on the continued importance of targeted approaches in newborn screening programmes.  
  Published 2015 ( European Society of Human Genetics ) ( P3G International Paediatric Platform) ( Human Genome Organisation) ( PHG Foundation)

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