Literature DB >> 23677179

The 'thousand-dollar genome': an ethical exploration.

Wybo J Dondorp1, Guido M W R de Wert.   

Abstract

Sequencing an individual's complete genome is expected to be possible for a relatively low sum 'one thousand dollars' within a few years. Sequencing refers to determining the order of base pairs that make up the genome. The result is a library of three billion letter combinations. Cheap whole-genome sequencing is of greatest importance to medical scientific research. Comparing individual complete genomes will lead to a better understanding of the contribution genetic variation makes to health and disease. As knowledge increases, the 'thousand-dollar genome' will also become increasingly important to healthcare. The applications that come within reach raise a number of ethical questions. This monitoring report addresses the issue.

Mesh:

Year:  2013        PMID: 23677179      PMCID: PMC3660958          DOI: 10.1038/ejhg.2013.73

Source DB:  PubMed          Journal:  Eur J Hum Genet        ISSN: 1018-4813            Impact factor:   4.246


  70 in total

1.  Newborn screening technology: proceed with caution.

Authors:  Jeffrey R Botkin; Ellen Wright Clayton; Norman C Fost; Wylie Burke; Thomas H Murray; Mary Ann Baily; Benjamin Wilfond; Alfred Berg; Lainie Friedman Ross
Journal:  Pediatrics       Date:  2006-05       Impact factor: 7.124

Review 2.  [Rapid prenatal diagnosis of chromosomal abnormalities; limitations and possibilities].

Authors:  L P ten Kate
Journal:  Ned Tijdschr Geneeskd       Date:  2006-07-22

3.  A vision of the future of newborn screening.

Authors:  Duane Alexander; Peter C van Dyck
Journal:  Pediatrics       Date:  2006-05       Impact factor: 7.124

4.  Neonatal screening: old dogma or sound principle?

Authors:  Nicholas Wald
Journal:  Pediatrics       Date:  2007-02       Impact factor: 7.124

5.  Microarray genetic screening: a prenatal roadblock for life?

Authors:  Evelyne Shuster
Journal:  Lancet       Date:  2007-02-10       Impact factor: 79.321

6.  Gene sequencing. The race for the $1000 genome.

Authors:  Robert F Service
Journal:  Science       Date:  2006-03-17       Impact factor: 47.728

Review 7.  Comparative genomic hybridization and prenatal diagnosis.

Authors:  Ignatia B Van den Veyver; Arthur L Beaudet
Journal:  Curr Opin Obstet Gynecol       Date:  2006-04       Impact factor: 1.927

Review 8.  Deciphering the role of heterozygous mutations in genes associated with parkinsonism.

Authors:  Christine Klein; Katja Lohmann-Hedrich; Ekaterina Rogaeva; Michael G Schlossmacher; Anthony E Lang
Journal:  Lancet Neurol       Date:  2007-07       Impact factor: 44.182

Review 9.  Screening for conditions that do not meet the Wilson and Jungner criteria: the case of Duchenne muscular dystrophy.

Authors:  Lainie Friedman Ross
Journal:  Am J Med Genet A       Date:  2006-04-15       Impact factor: 2.802

10.  Prenatal diagnosis of chromosomal abnormalities using array-based comparative genomic hybridization.

Authors:  Trilochan Sahoo; Sau Wai Cheung; Patricia Ward; Sandra Darilek; Ankita Patel; Daniela del Gaudio; Sung Hae L Kang; Seema R Lalani; Jiangzhen Li; Sallie McAdoo; Audrey Burke; Chad A Shaw; Pawel Stankiewicz; A Craig Chinault; Ignatia B Van den Veyver; Benjamin B Roa; Arthur L Beaudet; Christine M Eng
Journal:  Genet Med       Date:  2006-11       Impact factor: 8.822

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  23 in total

1.  Next generation sequencing for newborn screening: are we there yet?

Authors:  Eitan Friedman
Journal:  Genet Res (Camb)       Date:  2015-09-22       Impact factor: 1.588

2.  Challenges of using next generation sequencing in newborn screening.

Authors:  Eyal Reinstein
Journal:  Genet Res (Camb)       Date:  2015-11-02       Impact factor: 1.588

3.  Regulating biobanking with children's tissue: a legal analysis and the experts' view.

Authors:  Elcke J Kranendonk; M Corrette Ploem; Raoul C M Hennekam
Journal:  Eur J Hum Genet       Date:  2015-04-15       Impact factor: 4.246

4.  Expanded carrier screening panels-does bigger mean better?

Authors:  Sara Wienke; Kimberly Brown; Meagan Farmer; Charlie Strange
Journal:  J Community Genet       Date:  2013-09-24

5.  A Family-Centered Model for Sharing Genetic Risk.

Authors:  Mary B Daly
Journal:  J Law Med Ethics       Date:  2015       Impact factor: 1.718

6.  Sequencing Newborns: A Call for Nuanced Use of Genomic Technologies.

Authors:  Josephine Johnston; John D Lantos; Aaron Goldenberg; Flavia Chen; Erik Parens; Barbara A Koenig
Journal:  Hastings Cent Rep       Date:  2018-07       Impact factor: 2.683

7.  The Ethics of General Population Preventive Genomic Sequencing: Rights and Social Justice.

Authors:  Clair Morrissey; Rebecca L Walker
Journal:  J Med Philos       Date:  2018-01-12

8.  Big Data Privacy in Biomedical Research.

Authors:  Shuang Wang; Luca Bonomi; Wenrui Dai; Feng Chen; Cynthia Cheung; Cinnamon S Bloss; Samuel Cheng; Xiaoqian Jiang
Journal:  IEEE Trans Big Data       Date:  2016-09-13

9.  Rapid Challenges: Ethics and Genomic Neonatal Intensive Care.

Authors:  Christopher Gyngell; Ainsley J Newson; Dominic Wilkinson; Zornitza Stark; Julian Savulescu
Journal:  Pediatrics       Date:  2019-01       Impact factor: 7.124

Review 10.  Genomic Testing in The Paediatric Population: Ethical Considerations in Light of Recent Policy Statements.

Authors:  Ainsley J Newson; Lisa Schonstein
Journal:  Mol Diagn Ther       Date:  2016-10       Impact factor: 4.074

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