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Preparing DNA Libraries for Multiplexed Paired-End Deep Sequencing for Illumina GA Sequencers
Whole genome sequencing, also known as deep sequencing, is becoming a more affordable and efficient way to identify SNP mutations, deletions and insertions in DNA sequences across several different strains. Two major obstacles preventing the widespread use of deep sequencers are the costs involved i...
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| Main Authors: | , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2011
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| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3076644/ https://ncbi.nlm.nih.gov/pubmed/21400673 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/9780471729259.mc01e04s20 |
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