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The sequences were analyzed using the BiQ Analyzer program [ 27]; conversion rates were found to be between 96% and 100%.
PCR products were sequenced in the ABI 3130XL capillary genetic analyzer and sequences were analyzed using the Sequencher software.
The sequences were analyzed using the software Sequence Analyzer with the Base Caller Cimarron 3.12.
Sequences were analyzed using the Sequencer software (Gene Codes, Ann Arbor, MI).
Typical sequences were analyzed using the NCBI BLAST database to identify the closest relatives.
Nucleotide and deduced amino acid sequences were analyzed using the BioNumerics software v7.1.
Sequences were analyzed using the BioEdit program [11].
Then, sequences were analyzed using the sliding-window technique.
The N terminal sequences were analyzed using the SignalP algorithm [38].
The sequences were analyzed using the Jalview multiple alignment editor [41].
The DNA and deduced protein sequences were analyzed using the program "JustBio" at http://www.justbio.com.justbio.com
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