Evaluation of Single-Molecule Sequencing Technologies for Structural Variant Detection in Two Swedish Human Genomes

Long-read single molecule sequencing is increasingly used in human genomics research, as it allows to accurately detect large-scale DNA rearrangements such as structural variations (SVs) at high resolution. However, few studies have evaluated the performance of different single molecule sequencing p...

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Detalles Bibliográficos
Autores principales: Fatima, Nazeefa, Petri, Anna, Gyllensten, Ulf, Feuk, Lars, Ameur, Adam
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7760597/
https://www.ncbi.nlm.nih.gov/pubmed/33266238
http://dx.doi.org/10.3390/genes11121444

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7760597/
https://www.ncbi.nlm.nih.gov/pubmed/33266238
http://dx.doi.org/10.3390/genes11121444

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