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EGAS00001000322-sc-20130604 - samples

ABSTRACT: This project is to develop and validate a method to detect de novo mutations in a foetal genome through deep sequencing of cell-free DNA from the plasma of pregnant women. This data is part of a pre-publication release. For information on the proper use of pre-publication data shared by the Wellcome Trust Sanger Institute (including details of any publication moratoria), please see http://www.sanger.ac.uk/datasharing/

PROVIDER: EGAD00001000596 | EGA |

REPOSITORIES: EGA

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De novo mutations in cell free foetal DNA cffDNA

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