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We developed MSP primers based on these sequencing results.
Based on these sequencing results a primer (OVATE FOR 5) was designed and used along with primer OVATE REV1, for the amplification of a fragment belonging to the 5' upstream region from cv. "Round", which was sequenced too.
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Based on these sequences, a library was built containing nucleotide- and peptide-based tools capable of simultaneously targeting key cancer pathways or other diseases with a strong genetic background.
Based on these sequences, a strain-specific primer was designed for the amplification of one of the ISRs.
Strain-specific (SS) primers were developed based on these sequences.
Based on these sequence analyses, putative BVMO-encoding genes were identified.
Primer sets were designed based on these sequences and evaluated by PCR assays.
Based on these sequences, new primer sets were designed for specific identification of these two parasites by multiplex PCR.
Based on these sequences, we were able to design species-specific PCR primers for the precise identification of S. tundra.
Based on these sequences, phylogenetic trees were inferred which revealed a high degree of variability among the PRRSV Italian strains.
Based on these sequences, we statistically analyse the way in which graph colouring heuristics are automatically hybridised.
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