DNA methylation signature classification of rare disorders using publicly available methylation data
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Originalsprog | Engelsk |
---|---|
Tidsskrift | Clinical Genetics |
Vol/bind | 103 |
Udgave nummer | 6 |
Sider (fra-til) | 688-692 |
Antal sider | 5 |
ISSN | 0009-9163 |
DOI | |
Status | Udgivet - 2023 |
Bibliografisk note
Funding Information:
We acknowledge Darci T. Butcher and colleagues for making the methylation data available for public use. Several of the authors of this publication are members of the European Reference Network on Rare Congenital Malformations and Rare Intellectual Disability ERN‐ITHACA (EU Framework Partnership Agreement ID: 3HP‐HP‐FPA ERN‐01‐2016/739516). This work was supported, in part, by the Italian Ministry of Health (Ricerca Corrente 2021, to Andrea Ciolfi; 5x1000 2021 and RCR‐2020‐23670068_001, to Marco Tartaglia), Italian Ministry of Research (FOE 2019, to Marco Tartaglia), A.P. Møller Fonden (20‐L‐0371, to Mathis Hildonen), Familien Hede Nielsens Fond (2021‐0010, to Mathis Hildonen), and OUH & RH fælles forskningspulje (A4734, to Zeynep Tümer).
Publisher Copyright:
© 2023 The Authors. Clinical Genetics published by John Wiley & Sons Ltd.
ID: 363269700