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The results can also be alluded to the fact that the detection methods were designed to detect the non harmonic content in the signal.
Species-specific primers (given "RT" designation in the primer name) were designed to detect protein-coding sequences from cDNA.
Molecular probes were designed to detect genes coding for various oxygenase systems.
Experiments were designed to detect cumulative effects on accessory sex glands as well.
DNA RNA chimeric probes (cycling probes) were designed to detect the SNP at nucleotide 105705.
The sequences of oligonucleotides were designed to detect the H1N1 virus gene.
Short (9 bases) and specific probes were designed to detect SNP in TGF-β1.
RFLP assays were designed to detect each of the variant CYP1A1 alleles.
RT-PCR primers were designed to detect each of the eight rat mGluR transcripts.
Reverse transcription-LAMP (RT-LAMP) primers were designed to detect HuNoVs genogroups I (GI) and GII.
RT-PCR primers were designed to detect bunyavirus RNA in these samples.
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