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A Human Genome Structural Variation Sequencing Resource Reveals Insights into Mutational Mechanisms
Understanding the prevailing mutational mechanisms responsible for human genome structural variation requires uniformity in the discovery of allelic variants and precision in terms of breakpoint delineation. We develop a resource based on capillary end-sequencing of 13.8 million fosmid clones from 1...
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| Main Authors: | , , , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2010
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3026629/ https://ncbi.nlm.nih.gov/pubmed/21111241 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.cell.2010.10.027 |
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