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Data was assembled and analyzed.
Primary sequence data was assembled and the consensus sequence from each amplicon was generated using the sequence software BioNumerics 5.1.
All data was assembled and analysed using Microsoft Excel and GraphPad Prism.
All of the data was assembled and provided a new database for the discovery of IiDIRs.
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These data were assembled and subjected to automated primer walking, before re-assembly using PHRAP (P Green) and then passed into directed manual finishing for completion to phase 3 (50), where the estimated error rate is less than 1/100 000 (33).
The best available data were assembled and used in the analysis.
Microsatellite data were scored in GENEMAPPER v.3.7 (Applied Biosystems) and sequence data were assembled and manually checked in GENEIOUS v.4.7.6 (Biomatters, Auckland, New Zealand).
Effective oversight depends on how these data are assembled and maintained in the short and long term and who does the job on behalf of the board.
Field data were assembled and analyzed, and different planning alternatives were proposed and tested in order to design three future scenarios.
Sequence data were assembled and visualized using Phred/Phrap/Consed software (www.phrap.com).
All raw data were assembled and analyzed by two individuals independently and blinded to the analyses performed by the other.
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