Independent report

Implications of whole genome sequencing for newborn screening

Findings from a public dialogue.

Documents

Implications of whole genome sequencing for newborn screening (full report)

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Details

The implications of whole genome sequencing (WGS) for newborn screening public dialogue was commissioned in September 2020 by Genomics England and the UK National Screening Committee (UK NSC) with support from UK Research and Innovation’s Sciencewise programme.

Alongside the full report, you can view the executive summary in accessible format.

Updates to this page

Published 8 July 2021

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