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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Publicado no:Transl Psychiatry
Main Authors: Linthorst, Jasper, Meert, Wim, Hestand, Matthew S., Korlach, Jonas, Vermeesch, Joris Robert, Reinders, Marcel J. T., Holstege, Henne
Formato: Artigo
Idioma:Inglês
Publicado em: Nature Publishing Group UK 2020
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC7608644/
https://ncbi.nlm.nih.gov/pubmed/33139705
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41398-020-01060-5
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