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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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| Publicado no: | BioData Min |
|---|---|
| Main Authors: | , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2014
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| Assuntos: | |
| Acesso em linha: | 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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