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Massively Parallel Sequencing Approaches for Characterization of Structural Variation

The emergence of next-generation sequencing (NGS) technologies offers an incredible opportunity to comprehensively study DNA sequence variation in human genomes. Commercially available platforms from Roche (454), Illumina (Genome Analyzer and Hiseq 2000), and Applied Biosystems (SOLiD) have the capa...

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Bibliografske podrobnosti
Main Authors: Koboldt, Daniel C., Larson, David E., Chen, Ken, Ding, Li, Wilson, Richard K.
Format: Artigo
Jezik:Inglês
Izdano: 2012
Teme:
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC3679911/
https://ncbi.nlm.nih.gov/pubmed/22228022
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/978-1-61779-507-7_18
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