Sentence examples for analysis of the parental from inspiring English sources

An overview of the respective underlying number of datasets available for the analysis is shown in the flowchart in Figure 1. Figure 1 Overview of datasets available for the analysis of the parental willingness to pay (WTP).

MS/MS analysis of the parental ion at m/z 510.736 identified Glu362 in the sequence of the tryptic peptide FAE*IESK (with E* indicating EPG-modified glu) as the site of EPG attachment (Fig. 4A).

A comparison using contingency analysis of the parental and caregiver evaluations of overall behavioral pain reactivity type showed no significant relationship between the ratings obtained in the two situations.

In contrast, analysis of the HA-eEF1A E362D mutant revealed a tryptic fragment with m/z 809.404 and 405.206, representing the [M+H]+ and [M+2H]2+ ions of the unmodified heptapeptide FADIESK (results not shown; see also Table 1), with MS/MS analysis of the parental ion at m/z 405.206 confirming the absence of EPG (Fig. 4B).

Analysis of the parental documents ensured that 14 school-children were excluded for failing to meet the inclusion criteria.

Deletion of the gene was confirmed by Southern blot analysis of the parental line (data not shown) and two clonal lines derived from the parental line (Fig. S4).

Our analysis of the differential parental genome dosage effects on the endosperm development in the reciprocal interploidy crosses suggests distinct roles of parental genomes in seed development, with maternal genome functions to promote the endosperm cellularization and paternal genome functions to delay or inhibit cellularization potentially.

Analysis of the 42 parental stock specimens revealed 14 variable sites (1 transversion, 13 transitions), which defined 6 haplotypes (Table 1).

Time for downstream analysis of the findings (parental testing, validation by an alternative genetic test, etc).

The experimental MPVs enabled unequivocal exclusion of those genes for which the detected biased expression was due to differential hybridization affinity by the parental species' cDNAs to the same array, and therefore, allowed analysis of the bona fide parental expression dominance genes resulting from allohexaploidy-specified tuning.

RT-qPCR analysis of cultures of the parental and transfected parasite lines provided evidence of constitutive blood-stage expression of the introduced transgenes.