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Copy Number Variation detection from 1000 Genomes project exon capture sequencing data
BACKGROUND: DNA capture technologies combined with high-throughput sequencing now enable cost-effective, deep-coverage, targeted sequencing of complete exomes. This is well suited for SNP discovery and genotyping. However there has been little attention devoted to Copy Number Variation (CNV) detecti...
Αποθηκεύτηκε σε:
| Κύριοι συγγραφείς: | , , , , , , |
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| Μορφή: | Artigo |
| Γλώσσα: | Inglês |
| Έκδοση: |
BioMed Central
2012
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| Θέματα: | |
| Διαθέσιμο Online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3563612/ https://ncbi.nlm.nih.gov/pubmed/23157288 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2105-13-305 |
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