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Improved detection of global copy number variation using high density, non-polymorphic oligonucleotide probes
BACKGROUND: DNA sequence diversity within the human genome may be more greatly affected by copy number variations (CNVs) than single nucleotide polymorphisms (SNPs). Although the importance of CNVs in genome wide association studies (GWAS) is becoming widely accepted, the optimal methods for identif...
Αποθηκεύτηκε σε:
| Κύριοι συγγραφείς: | , , , , , , , , , , |
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| Μορφή: | Artigo |
| Γλώσσα: | Inglês |
| Έκδοση: |
BioMed Central
2008
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| Θέματα: | |
| Διαθέσιμο Online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2374799/ https://ncbi.nlm.nih.gov/pubmed/18373861 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2156-9-27 |
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