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Molecular markers were derived from SNPs identified between the sequenced and annotated VW9 genome and de novo sequence of VW8.
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Substantial genetic differences exist between the sequenced tomato accessions and the reference sequence.
All of these data indicate of a degree of informational degeneracy between the sequence and folding codes.
We preformed real-time quantitative PCR (q-PCR) experiments for selected 30 miRNAs in 47 tissue-specific samples and found agreement between the sequencing and q-PCR data.
The hidden data can be viewed as the alignment between the sequence and the model.
The matrix score calculates a match between the sequence and the matrix.
We enforce this physical constraint when generating the optimal alignment between the sequence and template.
Discrepancies between the sequence and the consensus may be automatically highlighted by either color or symbol.
Thus, we broke correspondence between the sequence and the resistance value.
ORM is used to calculate matching scores between the sequence and contigs.
Optimal genotype concordance (100%) was observed between the sequence and TaqMan.
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