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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...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Egile Nagusiak: Daines, Bryce, Wang, Hui, Li, Yumei, Han, Yi, Gibbs, Richard, Chen, Rui
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: Genetics Society of America 2009
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
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