Linear amplification for deep sequencing - PubMed (original) (raw)
. 2011 Jun 23;6(7):1026-36.
doi: 10.1038/nprot.2011.345.
Affiliations
- PMID: 21720315
- DOI: 10.1038/nprot.2011.345
Linear amplification for deep sequencing
Wieteke A M Hoeijmakers et al. Nat Protoc. 2011.
Abstract
Linear amplification for deep sequencing (LADS) is an amplification method that produces representative libraries for Illumina next-generation sequencing within 2 d. The method relies on attaching two different sequencing adapters to blunt-end repaired and A-tailed DNA fragments, wherein one of the adapters is extended with the sequence for the T7 RNA polymerase promoter. Ligated and size-selected DNA fragments are transcribed in vitro with high RNA yields. Subsequent cDNA synthesis is initiated from a primer complementary to the first adapter, ensuring that the library will only contain full-length fragments with two distinct adapters. Contrary to the severely biased representation of AT- or GC-rich fragments in standard PCR-amplified libraries, the sequence coverage in T7-amplified libraries is indistinguishable from that of nonamplified libraries. Moreover, in contrast to amplification-free methods, LADS can generate sequencing libraries from a few nanograms of DNA, which is essential for all applications in which the starting material is limited.
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References
- Dev Cell. 2009 Sep;17(3):425-34 - PubMed
- Exp Cell Res. 2010 May 1;316(8):1339-43 - PubMed
- Nucleic Acids Res. 2008 Sep;36(16):e105 - PubMed
- Nat Rev Genet. 2009 Oct;10(10):669-80 - PubMed
- Nat Rev Genet. 2009 Jan;10(1):57-63 - PubMed
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