Ultra-Low DNA Input into Whole Genome Methylation Assays and Detection of Oncogenic Methylation and Copy Number Variants in Circulating Tumour DNA
- DOI
- 10.3390/epigenomes5010006
- Published
- 02
- Container
- Epigenomes
- Publisher
- Not recorded
- Open access
- yes
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Cite this work
BibTeX
@article{allodium:10.3390/epigenomes5010006,
title = {Ultra-Low DNA Input into Whole Genome Methylation Assays and Detection of Oncogenic Methylation and Copy Number Variants in Circulating Tumour DNA},
author = {Celina Whalley and Karl Payne and Enric Domingo and Andrew Blake and Susan Richman and Jill Brooks and Nikolaos Batis and Rachel Spruce and S-CORT Consortium and Hisham Mehanna and Paul Nankivell and Andrew D. Beggs},
year = {2021},
journal = {Epigenomes},
doi = {10.3390/epigenomes5010006},
url = {https://doi.org/10.3390/epigenomes5010006}
}RIS
TY - JOUR TI - Ultra-Low DNA Input into Whole Genome Methylation Assays and Detection of Oncogenic Methylation and Copy Number Variants in Circulating Tumour DNA AU - Celina Whalley AU - Karl Payne AU - Enric Domingo AU - Andrew Blake AU - Susan Richman AU - Jill Brooks AU - Nikolaos Batis AU - Rachel Spruce AU - S-CORT Consortium AU - Hisham Mehanna AU - Paul Nankivell AU - Andrew D. Beggs PY - 2021 JO - Epigenomes DO - 10.3390/epigenomes5010006 UR - https://doi.org/10.3390/epigenomes5010006 ER -
APA
Whalley, C., Payne, K., Domingo, E., Blake, A., Richman, S., Brooks, J., Batis, N., Spruce, R., Consortium, S., Mehanna, H., Nankivell, P., & Beggs, A. D. (2021). Ultra-Low DNA Input into Whole Genome Methylation Assays and Detection of Oncogenic Methylation and Copy Number Variants in Circulating Tumour DNA. Epigenomes. https://doi.org/10.3390/epigenomes5010006
Source records
- doaj · retrieved 2026-11-10T10:47:34.452Z