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Exact(17)
For all qRT-PCR measurements, the abundance of each transcript was measured relative to that of RPLP0.
The expression of HER2 transcript was measured by quantitative real-time reverse-transcription assay in MUC4-transfected SKOV3 cells.
RNA was extracted and the major E1A 13S transcript was measured by RT-QPCR.
Then, the RPKM value for each transcript was measured in reads per kilobase of transcript sequence per million mapped reads [21].
The 'consistency' values (shown in the result tables) indicate the number of replicates in which a similar direction of change was seen for each transcript, in the replicates in which the transcript was measured.
The abundance of each mRNA transcript was measured and expressed in comparison to glyceraldehyde 3-phosphate dehydrogenase (GAPDH).
Similar(43)
This might be due to the time-course of the latter gene expression, the transcript being measured after 3 h of monocyte activation and that of secreted proteins after 24 h.
Each transcript is measured by 11 20 probesets, where a probeset consists of two almost identical sequences of length 25 bp.
Levels of human lamin A and progerin transcript were measured by quantitative RT-PCR (qRT-PCR) as previously described (41).
The relative abundances of each transcript were measured by SYBR Green real-time PCR and analyzed according to the comparative C t method.
The expression abundance of transcripts was measured by the number of tags mapped.
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