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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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| 主要な著者: | , |
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| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
2011
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| オンライン･アクセス: | 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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