This section proposes a test that addresses the stated requirement.
This section proposed several research and implementation gaps that require attention.
As discussed in Section 4.3.3, van der Sandt (1992) proposes that presuppositions whose descriptive content is relatively poor are hard to accommodate.
In this section, we propose that core self-evaluations can serve as a bridge to link these two constructs.
In this section, we propose that additional crucial steps are needed to move the field forward and accelerate the clinical adoption of whole exome or genome sequencing.
In this section, a novel approach is proposed that is based upon the integration of usability testing [1], conventional heuristic evaluation [31 33], ISO 9241-151 guidelines [26, 27] and data-mining knowledge discovery process [12, 49].
In a final section, a statistical framework is proposed that provides estimates of this distribution of DS.
In this section, we propose techniques that make use of the user separation and block size estimation methods proposed in the previous sections in order to improve the opportunity detection performance.
To recapitulate, in this section, we have proposed that the origin of linear chromosomes (genomes in pieces) was a eukaryotic innovation generated by the mobilization of group II intron-derived retroelements as a response to endosymbiosis stress (McClintock 1984; Koonin 2011).
In this section, we propose a method that requires no connection to the AP and no NAV duration reading.
In this section, we propose a framework that expresses a user's presence through a virtual human in a video conference.
