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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...
Tallennettuna:
| Päätekijät: | , , , , |
|---|---|
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
2012
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| Aiheet: | |
| Linkit: | 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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