Cost-effective DNA methylation profiling by FML-seq.


Journal

Life science alliance
ISSN: 2575-1077
Titre abrégé: Life Sci Alliance
Pays: United States
ID NLM: 101728869

Informations de publication

Date de publication:
12 2023
Historique:
received: 17 08 2023
revised: 20 09 2023
accepted: 21 09 2023
medline: 5 10 2023
pubmed: 30 9 2023
entrez: 29 9 2023
Statut: epublish

Résumé

Current methods for profiling DNA methylation require costly reagents, sequencing, and labor time. We introduce fragmentation at methylated loci and sequencing (FML-seq), a sequencing library protocol that greatly reduces all these costs. Relative to other techniques tested on the same human cell lines, FML-seq produces similar measurements of absolute and differential cytosine methylation at a fraction of the price. FML-seq enables inexpensive, high-throughput experimental designs for large-scale epigenetics research projects.

Identifiants

pubmed: 37775270
pii: 6/12/e202302326
doi: 10.26508/lsa.202302326
pmc: PMC10546043
pii:
doi:

Substances chimiques

Fluorometholone SV0CSG527L

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : NCI NIH HHS
ID : R01 CA193694
Pays : United States

Commentaires et corrections

Type : UpdateOf

Informations de copyright

© 2023 Foley et al.

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Auteurs

Joseph W Foley (JW)

Department of Pathology, Stanford University School of Medicine, Stanford, CA, USA jwfoley@nus.edu.sg.

Shirley X Zhu (SX)

Department of Pathology, Stanford University School of Medicine, Stanford, CA, USA.

Robert B West (RB)

Department of Pathology, Stanford University School of Medicine, Stanford, CA, USA.

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Classifications MeSH