Sentence examples for pmi i from inspiring English sources

and SINR i r = P r α i, r r h i, r r H w PMI i r r 2 σ 2 + 2 N t m P m α i, r m. (24).

The RRH non-central area user determines the preferred codeword, the company cluster, and computes the SINR as PMI i r = max j = 1, …, I r h i, r r H w j r (25).

The details are given as follows:  The RRH central area user determines the preferred codeword and computes the SINR as PMI i r = max j = 1, …, I r h i, r r H w j r (23).

The RRH central area user determines the preferred codeword and computes the SINR as PMI i r = max j = 1, …, I r h i, r r H w j r (23).

The macro non-central area user determines the preferred codeword index PMI i m, the company cluster index P i m, and the SINR using the method similar to that of the RRH non-central area user.

The macro central area user determines the preferred codeword index PMI i m and computes SINR i m using the method similar to that of the RRH central area user.

The sample selection allowed us to establish the expression dynamics of these key cell-cycle regulators pre- and post-PMII in angiosperms with bicellular pollen.

Semi-quantitative RT-PCR analysis showed that the expression of FBL12 and FBL21 peaked at the 'division window' followed by a rapid decline post-PMII.

We used semi-quantitative RT-PCR to validate the expression of selected target genes and to extend the analysis post-PMII after 13, 24 and 48 h of pollen-tube growth.

The extended analysis of post-PMII stages provided additional information not obtained by microarrays to understand gene expression and mRNA stability in relation to gene function in the course of pollen-tube extension.

We selected nine candidate genes to verify their microarray expression profiles by real-time qRT-PCR at the two developmental stages used for microarray analysis (MPG and PT4) and extended the analysis to three developmental stages post-PMII (13 , 24and 48 h after in vitro pollen germination).