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This article also presents the experiments using a real video sequence to verify the proposed method.
Experiments were performed with "Mobile" sequence to verify the effectiveness of our method in managing the additional bandwidth requirement because of SSP-frames at the switching instants.
Plasmid inserts were then sequenced and compared to their respective reference sequence to verify the identity of nc5, arnp and ron4 cloned fragments, as well as the efficacy of the sequencing primers for the pELMO vector (ccdBsec-F and ccdBsec-R) compared to those for the pGEM-T Easy vector (SP6 and T7).
Sequences were aligned to the genome sequence to verify that the correct gene had been amplified.
Sanger sequencing of the cloned viral genome was performed to confirm the original metagenomic sequence, to verify circularity, and to allow ORF prediction.
BLAST analysis [ 29] was performed with the gDNA target sequence to verify the specificity through the lack of homology with other crops/cultivars.
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Other researchers used DNA sequencing to verify those results.
All the plasmids were sequenced to verify the sequence.
PCR products were sequenced to verify the specificity of the reaction.
The amplicons were cloned and sequenced to verify the encoding region.
This paper also presents experiments using real video sequences to verify the proposed method.
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