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The z value vector was then multiplied by the appropriate coefficient vector.
The vector was then applied to deliver virus infectious clones to the nuclei of plant cells.
The composite feature vector was then fed to a number of statistical classifiers.
The binary vector was then used to introduce the OsNCED3::GUS or OsNCED4::GUS constructs into Japonica rice variety TNG67.
The resulting vector was then used to delete yfiB by two-step allelic exchange (Hmelo et al., 2015).
A document vector was then generated for each document, encoding the absence or presence of the remaining terms in a binary string (Table 2).
To down-regulate the expression level of the gene or lead to the loss-of-function of the gene, the vector was then introduced into rice via Agrobacterium-mediated transformation.
The vector was then transformed and expressed as per the manufacturers directions.
This vector was then injected into one-cell stage embryos with meganuclease I-SceI [88] [89].
The sequence of pEGFP-Luc2 vector was then confirmed both by restriction mapping and DNA sequencing of the plasmid.
Vector was then titered for DNase-resistant vector genomes by real time PCR relative to a standard.
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