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High-Throughput Multiplex Sequencing to Discover Copy Number Variants in Drosophila
Copy number variation (CNV) contributes in phenotypically relevant ways to the genetic variability of many organisms. Cost-effective genomewide methods for identifying copy number variation are necessary to elucidate the contribution that these structural variants make to the genomes of model organi...
Gorde:
| Egile Nagusiak: | , , , , , |
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| Formatua: | Artigo |
| Hizkuntza: | Inglês |
| Argitaratua: |
Genetics Society of America
2009
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| Gaiak: | |
| Sarrera elektronikoa: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2728881/ https://ncbi.nlm.nih.gov/pubmed/19528327 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1534/genetics.109.103218 |
| Etiketak: |
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