| Literature DB >> 23900195 |
Makio Kihana1, Fuzuki Mizuno, Rikai Sawafuji, Li Wang, Shintaroh Ueda.
Abstract
Due to the difficulties in deep sequencing, high-throughput sequencing of ancient DNA has been limited to exceptionally well-preserved ancient materials. The primary factor is microbial attack popularly observed in the buried materials, and it causes drastic increase in relative ratio of microbial DNA in the extracted DNA. We present a unified strategy in which emulsion PCR is coupled with target enrichment followed by next-generation sequencing. The method made it possible to obtain efficiently non-duplicated reads mapped to target sequences of interest, and this can achieve deep and reliable sequencing of ancient DNA from typical materials, even though poorly preserved.Keywords: Ancient DNA; Emulsion PCR; Microbial attack; NGS; Next-generation sequencing; PCR; Target enrichment; UV; double-stranded DNA; dsDNA; kDa; kilo-dalton; next-generation sequencing; polymerase-chain reaction; ultraviolet
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Year: 2013 PMID: 23900195 DOI: 10.1016/j.gene.2013.07.040
Source DB: PubMed Journal: Gene ISSN: 0378-1119 Impact factor: 3.688