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De-identified clinical data is assembled and entered so that it will be available along with the TMA recipient (or mother) block, tissue sections and tissue section virtual images.
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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).
Data was assembled and analyzed.
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.
All raw data were assembled and analyzed by 2 individuals blinded to the analysis (JH and JL).
DNA sequence data were assembled and aligned using the Lasergene software package (DNASTAR, Madison, WI, USA) and MacClade.
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