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Genome-Wide Identification of Copy Number Variations in Chinese Holstein
Recent studies of mammalian genomes have uncovered the vast extent of copy number variations (CNVs) that contribute to phenotypic diversity. Compared to SNP, a CNV can cover a wider chromosome region, which may potentially incur substantial sequence changes and induce more significant effects on phe...
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Main Authors: | , , , , , |
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Formato: | Artigo |
Idioma: | Inglês |
Publicado em: |
Public Library of Science
2012
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Assuntos: | |
Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3492429/ https://ncbi.nlm.nih.gov/pubmed/23144949 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0048732 |
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