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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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Autori principali: Koboldt, Daniel C., Larson, David E., Chen, Ken, Ding, Li, Wilson, Richard K.
Natura: Artigo
Lingua:Inglês
Pubblicazione: 2012
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Accesso online: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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