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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Detalles Bibliográficos
Autores principales: Handsaker, Robert E., Van Doren, Vanessa, Berman, Jennifer R., Genovese, Giulio, Kashin, Seva, Boettger, Linda M., McCarroll, Steven A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2015
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4405206/
https://www.ncbi.nlm.nih.gov/pubmed/25621458
http://dx.doi.org/10.1038/ng.3200

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4405206/
https://www.ncbi.nlm.nih.gov/pubmed/25621458
http://dx.doi.org/10.1038/ng.3200

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