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Genomic characteristics of cattle copy number variations
BACKGROUND: Copy number variation (CNV) represents another important source of genetic variation complementary to single nucleotide polymorphism (SNP). High-density SNP array data have been routinely used to detect human CNVs, many of which have significant functional effects on gene expression and...
Αποθηκεύτηκε σε:
| Κύριοι συγγραφείς: | , , , , , , , , , , , |
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| Μορφή: | Artigo |
| Γλώσσα: | Inglês |
| Έκδοση: |
BioMed Central
2011
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| Θέματα: | |
| Διαθέσιμο Online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3053260/ https://ncbi.nlm.nih.gov/pubmed/21345189 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2164-12-127 |
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