Independent report

Implications of whole genome sequencing for newborn screening

Findings from a public dialogue.

• From: UK National Screening Committee
• Published: 8 July 2021

Documents

Implications of whole genome sequencing for newborn screening (executive summary)

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

PDF, 1.55 MB, 108 pages

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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.

Published 8 July 2021