Extreme enrichment of VNTR-associated polymorphicity in human subtelomeres: genes with most VNTRs are predominantly expressed in the brain

The human genome harbors numerous structural variants (SVs) which, due to their repetitive nature, are currently underexplored in short-read whole-genome sequencing approaches. Using single-molecule, real-time (SMRT) long-read sequencing technology in combination with FALCON-Unzip, we generated a de...

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Detalles Bibliográficos
Autores principales: Linthorst, Jasper, Meert, Wim, Hestand, Matthew S., Korlach, Jonas, Vermeesch, Joris Robert, Reinders, Marcel J. T., Holstege, Henne
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7608644/
https://www.ncbi.nlm.nih.gov/pubmed/33139705
http://dx.doi.org/10.1038/s41398-020-01060-5

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7608644/
https://www.ncbi.nlm.nih.gov/pubmed/33139705
http://dx.doi.org/10.1038/s41398-020-01060-5

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