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In addition, a blended design scheme is also proposed, which is achieved by using the stacking sequence table technique.
Combining both the MinION and Illumina reads yielded a consensus YCNV sequence sharing 99.93% identity with the Sanger determined YCNV sequence (Table 3).
This article introduces the concept of stacking sequence table (SST) for the optimal design of laminated composite structures with ply drops.
While the genome coverage of the mapped Illumina reads was better than that of the mapped MinION reads, the consensus YCNV sequences generated by both approaches shared more than 99.83% identity with the YCNV reference Sanger sequence (Table 3).
Overall, 195 million short-read sequences were produced and used for mapping onto the reference Nipponbare genome sequence (Table 1).
About 87 90% of the signatures matched to the japonica (Nipponbare) genomic sequence (Table S2 of the Electronic Supplementary Material).
Many represent only one viral cDNA sequence (Table 1).
Four OTUs contained only one sequence (Table S2).
Each actin synthetic peptide was recorded in relation to its amino acid sequence ("Table 2").
Another type of alteration of 23S rRNA genes is insertion of an intervening sequence (Table 3).
In the MFN2 gene, we identified four SNPs in the coding sequence (Table S1).
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