Deciphering complex genome rearrangements in C. elegans using short-read whole genome sequencing

Genomic rearrangements cause congenital disorders, cancer, and complex diseases in human. Yet, they are still understudied in rare diseases because their detection is challenging, despite the advent of whole genome sequencing (WGS) technologies. Short-read (srWGS) and long-read WGS approaches are re...

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Detalles Bibliográficos
Autores principales: Maroilley, Tatiana, Li, Xiao, Oldach, Matthew, Jean, Francesca, Stasiuk, Susan J., Tarailo-Graovac, Maja
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8440550/
https://www.ncbi.nlm.nih.gov/pubmed/34521941
http://dx.doi.org/10.1038/s41598-021-97764-9

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8440550/
https://www.ncbi.nlm.nih.gov/pubmed/34521941
http://dx.doi.org/10.1038/s41598-021-97764-9

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