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Security is provided by using random length of the forbidden symbols and randomly placing these dummy symbols in the probability table.
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To avoid the possibility of preferential amplification due to poly (A) tail length, we standardized the cDNA synthesis procedures by using random primers that can account for transcript abundances, irrespective of the poly (A) tail status.
Random variation between individuals was accounted for by using random intercepts.
RNA was reverse transcribed by using random hexamers as primers.
Trials were combined by using random effects meta-analysis.
Total RNA was reverse transcribed by using random hexamer primers.
Choice data were analyzed by using random-parameters logit.
Meta-analyses were performed by using random-effects models.
Participants were recruited by using random-digit dialing.
PSG9 expression patterns were analysed using random primed radiolabeled full-length PSG9 cDNA.
289, yielded a novel mammalian virus from the family Caliciviridae that we further characterized by near full-length genome sequencing using random amplification with next-generation sequencing, specific reverse transcription PCRs, and 3′ rapid amplification of cDNA ends PCR as described (6, 7 ).
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