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Large multi-allelic copy number variations in humans
Thousands of genome segments appear to be present in widely varying copy number in different human genomes. We developed ways to use increasingly abundant whole genome sequence data to identify the copy numbers, alleles and haplotypes present at most large, multi-allelic CNVs (mCNVs). We analyzed 84...
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| Publicado no: | Nat Genet |
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| Main Authors: | , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2015
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4405206/ https://ncbi.nlm.nih.gov/pubmed/25621458 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/ng.3200 |
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