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All gp120 sequences were determined using an ABI 3100 sequencer and assembled using Sequencher (www.genecodes.com).
Sequences were determined in an ABI 3730xl capillary sequencer.
The forward and the reverse sequences were determined for all samples using an ABI PRISM 377 DNA sequencer.
Full-length Gag virus sequences were determined in 15 individuals.
However, 4 different kinds of sequences were determined among the SpeI-AvaI nPCR amplicons.
Plasmids sequences were determined using an ABI PRISM 3130xl Genetic Analyzer (Life Technologies, CA, USA).
The flanking sequences were determined via inverse PCR (An et al. [2003]; Ryu et al. [2004]).
The amplified fragment was cloned, and the complete sequences were determined.
The total 845 base pairs of psbA sequences were determined and aligned in this study.
DNA sequences were determined using the direct DyeDeoxy Terminator Cycle method.
New target DNA sequences were determined for the detection of 19 bacterial pathogens.
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