Whole-Genome Sequencing in Newborn Screening Programs

Author:

Knoppers Bartha M.1,Sénécal Karine1,Borry Pascal2,Avard Denise1

Affiliation:

1. Department of Human Genetics, McGill University, Montreal, Quebec H3A OG1, Canada.

2. Department of Public Health and Primary Care, University of Leuven, Leuven, 3000 Leuven, Belgium.

Abstract

The possible introduction of whole-genome sequencing into newborn screening programs should proceed with caution.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

General Medicine

Reference34 articles.

1. What ethical and legal principles should guide the genotyping of children as part of a personalised screening programme for common cancer?

2. Centers for Disease Control and Prevention “Ten Great Public Health Achievements–United States 2001-2010 ” Morbidity and Mortality Weekly Report (Centers for Disease Control and Prevention Washington DC 2011); published online (www.cdc.gov/mmwr/pdf/wk/mm6019.pdf).

3. Developing a national newborn screening strategy for Canada;Wilson K.;Health Law Rev.,2010

4. Newborn screening: new developments, new dilemmas

5. C. Curtin ASHG panelists discuss interest in sequencing-based newborn screening. GenomeWeb (2013).

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