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SCAN database: facilitating integrative analyses of cytosine modification and expression QTL
Functional annotation of genetic variants including single nucleotide polymorphisms (SNPs) and copy number variations (CNV) promises to greatly improve our understanding of human complex traits. Previous transcriptomic studies involving individuals from different global populations have investigated...
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| Publicado no: | Database (Oxford) |
|---|---|
| Main Authors: | , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Oxford University Press
2015
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4375357/ https://ncbi.nlm.nih.gov/pubmed/25818895 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/database/bav025 |
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