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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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Detalhes bibliográficos
Publicado no:Genome Res
Main Authors: Sanders, Ashley D., Hills, Mark, Porubský, David, Guryev, Victor, Falconer, Ester, Lansdorp, Peter M.
Formato: Artigo
Idioma:Inglês
Publicado em: Cold Spring Harbor Laboratory Press 2016
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5088599/
https://ncbi.nlm.nih.gov/pubmed/27472961
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1101/gr.201160.115
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