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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Bibliographic Details
Main Authors: Kidd, Jeffrey M., Graves, Tina, Newman, Tera, Fulton, Robert, Hayden, Hillary S., Malig, Maika, Kallicki, Joelle, Kaul, Rajinder, Wilson, Richard K., Eichler, Evan E.
Format: Artigo
Language:Inglês
Published: 2010
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Article
Online Access: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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