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Genome-wide Mapping of Copy Number Variations Using SNP Arrays
The availability of high-density single nucleotide polymorphism (SNP) microarrays in recent years has proven to be a great step forward in the context of global analysis of genomic abnormalities in disease. SNP arrays offer great robustness, high resolution and the possibility to detect a variety of...
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| Asıl Yazarlar: | , , |
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| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
S. Karger GmbH
2009
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2941829/ https://ncbi.nlm.nih.gov/pubmed/21049075 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1159/000225372 |
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