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Elusive Copy Number Variation in the Mouse Genome
BACKGROUND: Array comparative genomic hybridization (aCGH) to detect copy number variants (CNVs) in mammalian genomes has led to a growing awareness of the potential importance of this category of sequence variation as a cause of phenotypic variation. Yet there are large discrepancies between studie...
Tallennettuna:
| Päätekijät: | , , , , , , , |
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| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
Public Library of Science
2010
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2943477/ https://ncbi.nlm.nih.gov/pubmed/20877625 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0012839 |
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