Characterizing polymorphic inversions in human genomes by single-cell sequencing

Identifying genomic features that differ between individuals and cells can help uncover the functional variants that drive phenotypes and disease susceptibilities. For this, single-cell studies are paramount, as it becomes increasingly clear that the contribution of rare but functional cellular subp...

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Detalles Bibliográficos
Autores principales: Sanders, Ashley D., Hills, Mark, Porubský, David, Guryev, Victor, Falconer, Ester, Lansdorp, Peter M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory Press 2016
Materias:
Method
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5088599/
https://www.ncbi.nlm.nih.gov/pubmed/27472961
http://dx.doi.org/10.1101/gr.201160.115

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5088599/
https://www.ncbi.nlm.nih.gov/pubmed/27472961
http://dx.doi.org/10.1101/gr.201160.115

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