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...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Argitaratua izan da:BioData Min
Egile Nagusiak: Laurila, Kirsti, Autio, Reija, Kong, Lingjia, Närvä, Elisa, Hussein, Samer, Otonkoski, Timo, Lahesmaa, Riitta, Lähdesmäki, Harri
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: BioMed Central 2014
Gaiak:
Research
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC4298950/
https://ncbi.nlm.nih.gov/pubmed/25649046
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13040-014-0032-2
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