Integrative genomics and transcriptomics analysis of human embryonic and induced pluripotent stem cells

BACKGROUND: Human genomic variations, including single nucleotide polymorphisms (SNPs) and copy number variations (CNVs), are associated with several phenotypic traits varying from mild features to hereditary diseases. Several genome-wide studies have reported genomic variants that correlate with ge...

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Detalles Bibliográficos
Autores principales: Laurila, Kirsti, Autio, Reija, Kong, Lingjia, Närvä, Elisa, Hussein, Samer, Otonkoski, Timo, Lahesmaa, Riitta, Lähdesmäki, Harri
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4298950/
https://www.ncbi.nlm.nih.gov/pubmed/25649046
http://dx.doi.org/10.1186/s13040-014-0032-2

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4298950/
https://www.ncbi.nlm.nih.gov/pubmed/25649046
http://dx.doi.org/10.1186/s13040-014-0032-2

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