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"The relocation will ensure that all newly assembled software can be verified by an independent organization, and show that software builds and updates received by customers match the source code provided for audit".
The transcriptome short reads were de novo assembled software following the protocol documented by Grabherr et al. [ 18].
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At present, with object-oriented programming the dominant paradigm, it is common to assemble software systems comprising components written in at least two different object-oriented languages.
E-speak could potentially find and assemble software from chunks of code or create teams of engineers for crash projects.
The GS FLX sequence data were assembled using Newbler assembly software.
The reads were assembled using SOAPdenovo assembler software [ 67] subsequently.
The sequence data were de novo assembled using Newbler assembly software.
The 454-reads were assembled using software version 2.3 Newbler, which has a cDNA option for transcriptome assembly.
Forward and reverse sequences were assembled using software Sequencher (GeneCodes).
However, even with the help of new assembling software, finishing a whole genome is a time-consuming task.
The clean reads were de novo assembled into 124,034 contigs with the assemble software of SOAPdenovo [27] (Table 1).
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