Performance comparisons of methylation and structural variants from low-input whole-genome methylation sequencing

AIM: Whole-genome methylation sequencing carries both DNA methylation and structural variant information (single nucleotide variant [SNV]; copy number variant [CNV]); however, limited data is available on the reliability of obtaining this information simultaneously from low-input DNA using various l...

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Detalles Bibliográficos
Autores principales: Sun, Zhifu, Behati, Saurabh, Wang, Panwen, Bhagwate, Aditya, McDonough, Samantha, Wang, Vivian, Taylor, William, Cunningham, Julie, Kisiel, John
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Future Medicine Ltd 2023
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10072131/
https://www.ncbi.nlm.nih.gov/pubmed/36919677
http://dx.doi.org/10.2217/epi-2022-0453

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10072131/
https://www.ncbi.nlm.nih.gov/pubmed/36919677
http://dx.doi.org/10.2217/epi-2022-0453

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