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Biological relevance of CNV calling methods using familial relatedness including monozygotic twins
BACKGROUND: Studies involving the analysis of structural variation including Copy Number Variation (CNV) have recently exploded in the literature. Furthermore, CNVs have been associated with a number of complex diseases and neurodevelopmental disorders. Common methods for CNV detection use SNP, CNV,...
Αποθηκεύτηκε σε:
| Κύριοι συγγραφείς: | , , , , , , |
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| Μορφή: | Artigo |
| Γλώσσα: | Inglês |
| Έκδοση: |
BioMed Central
2014
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| Θέματα: | |
| Διαθέσιμο Online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4021055/ https://ncbi.nlm.nih.gov/pubmed/24750645 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2105-15-114 |
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