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The TaqMan readings were analyzed using the "Sequence Detector" v1.6.3 software (Applied Biosystems).
Real-time PCR data were analyzed using the Sequence detector version 2.2.2 software supplied with the 7900 HT Fast-Real-Time Fast-Real-Time Fast-Real-Time PCR System Applied Biosystems
Real-time PCR amplification was performed using an Applied Biosystems 7900HT Real-Time PCR System and analyzed using the sequence detector software.
Data were analyzed using the Sequence Detector v1.9 software, and statistical analyses were performed using the R-statistical computing programming language (R Development Core Team 2006 R: a language and environment for statistical computing. R Foundation for Statistical Computing, Vienna, Austria.
Quantitative data was analyzed using the Sequence Detection System software (v1.0; Applied Biosystems).
Real-time data were analyzed using the Sequence Detection System 1.7 (Applied Biosystems).
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Results were analyzed using the sequencing analysis software for the sequencer (Version 1.5; AB Applied Biosystems, Foster City, CA, USA).
Sequences were analyzed using the Sequencer software (Gene Codes, Ann Arbor, MI).
The sequences were analyzed using the software Sequence Analyzer with the Base Caller Cimarron 3.12.
Sequencing results were analyzed using the BioEdit sequence alignment editor (Ibis Biosciences); primer sequences were removed and nucleotide similarity comparisons were made using the GenBank database.
Sequence polymorphisms were analyzed using the DNA Sequence Polymorphism (DnaSP5) software version 5.0 (Librado and Rozas 2009) and Molecular Evolutionary Genetics Analysis (MEGA5) software version 5.0 (Tamura et al. 2011).
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