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Our study found that 31%and75%5% of the study patients had concretions from the procedure of expression and syringing, respectively.
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The procedures for transfection of expression vectors of HA-p68, fluorescent proteins, and Crm1 and duplex RNAi were similar to our previous reports [ 30, 50].
The robust-multi-array average (RMA) method was used for the normalization procedure of the raw expression data.
Finally, the procedure of estimating the expression value of each target gene has a linear complexity.
Formation of the 3′ end of precursor messenger RNA (pre-mRNA) is an essential step in the procedure of eukaryotic gene expression.
The procedure of finding significant expression regions was also performed for intergenic spaces, to find the probable regions of novel transcription, not known by the curators of the annotations in Phytozome.
In this investigation we studied gene pair co-expression change by using a stochastic process model for approximating the underlying dynamic procedure of the co-expression change during cancer progression.
This procedure revealed expression of dsRNA in small clusters distributed across the cytoplasm and the nucleus, panels A and B).
According to this procedure, the expression of 18 315 and 18 795 known transcripts was detected in the primary ALL and relapse samples, respectively (Supplementary Data 2), showing that 62 and 64% of annotated human genes were transcribed in the examined stages of the disease.
The reduction procedure artificially decreased the sensitivity of expression profiles by reducing their size.
The reduction procedure artificially decreased the specificity of expression profiles by substituting top-ranked genes with false positives.
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