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Copy number variation in human genomes from three major ethno-linguistic groups in Africa
BACKGROUND: Copy number variation is an important class of genomic variation that has been reported in 75% of the human genome. However, it is underreported in African populations. Copy number variants (CNVs) could have important impacts on disease susceptibility and environmental adaptation. To des...
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| Publicado en: | BMC Genomics |
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| Main Authors: | , , , , , , , , , , , , , , , , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
BioMed Central
2020
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| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7147055/ https://ncbi.nlm.nih.gov/pubmed/32272904 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12864-020-6669-y |
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