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Isolates with results suggestive of mutations can be selected for sequence analysis in order to define the amino acid at the mutation site.
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Clones from these libraries were selected for sequence analysis on the basis of a heteroduplex mobility assay to maximise the diversity represented in the sample.
Only the sequences that included the complete gag open reading frame were selected for sequence analysis.
Out of these 20 clusters of genes, 7 that showed significant regulation were selected for sequence analysis (Table S4).
A total of 210 SFPs were selected for sequence validation.
Some CCNA1 methylation-positive CCs were selected for sequence analysis.
Additional genes were selected for sequence analysis based on clinical findings.
For each gastric biopsy library, at least 60 colonies were selected for sequencing.
Three clones were selected for sequencing and assembled into single var gene containing contigs.
After dot-blot and elimination of the most likely repetitive clones, 753 clones were selected for sequencing.
After performing MDA reactions, two replicate single-cell genomes were selected for sequencing on the Illumina platform.
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