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In these samples, enterovirus 96 was identified by sequence analysis utilizing a seminested PCR system.
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For these samples, enterovirus 96 was identified by sequence analysis of VP1 coding region utilizing a seminested PCR [ 12] (data not shown).
DNA sequences of the constructed plasmids were verified by sequence analysis (Eurofins Genomics, Tokyo, Japan).
These were verified by sequence analysis.
Sequence data analysis utilizes publicly available software supplemented by an expert-curated compendium of >2000 CFTR variants.
The absence of undesirable mutations in the OsIRE1 loci was confirmed by sequencing analysis.
Glaubitz, J.C. et al. TASSEL-GBS: a high capacity genotyping by sequencing analysis pipeline.
All constructs were verified by sequencing analysis.
Sequences were verified by sequencing analysis.
Real-time PCR and sequence analysis were utilized to identify Ha- and Ki- ras mutation (Gly -> Val).
Our preliminary analysis utilized sequence features for all amino acid residues in each protein, obtained from UniProt features records [ 13].
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