Reflections on the cost of "low-cost" whole genome sequencing: framing the health policy debate.

Published

Journal Article

The cost of whole genome sequencing is dropping rapidly. There has been a great deal of enthusiasm about the potential for this technological advance to transform clinical care. Given the interest and significant investment in genomics, this seems an ideal time to consider what the evidence tells us about potential benefits and harms, particularly in the context of health care policy. The scale and pace of adoption of this powerful new technology should be driven by clinical need, clinical evidence, and a commitment to put patients at the centre of health care policy.

Full Text

Cited Authors

  • Caulfield, T; Evans, J; McGuire, A; McCabe, C; Bubela, T; Cook-Deegan, R; Fishman, J; Hogarth, S; Miller, FA; Ravitsky, V; Biesecker, B; Borry, P; Cho, MK; Carroll, JC; Etchegary, H; Joly, Y; Kato, K; Lee, SS-J; Rothenberg, K; Sankar, P; Szego, MJ; Ossorio, P; Pullman, D; Rousseau, F; Ungar, WJ; Wilson, B

Published Date

  • November 5, 2013

Published In

Volume / Issue

  • 11 / 11

Start / End Page

  • e1001699 -

PubMed ID

  • 24223516

Pubmed Central ID

  • 24223516

Electronic International Standard Serial Number (EISSN)

  • 1545-7885

International Standard Serial Number (ISSN)

  • 1544-9173

Digital Object Identifier (DOI)

  • 10.1371/journal.pbio.1001699

Language

  • eng