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This paper reviews the efforts to date to identify and 'calibrate' WTP derived from one or more methods that involve assessment of hypothetical settings, be they (i) contingent valuation methods, (ii) choice experiments involving trading attributes between multiple alternatives, with or without referencing, or (iii) methods involving salient or non-salient incentives linked to actual behaviour.
Increasingly, healthcare decisions involve multiple alternatives with varying combinations of advantages and disadvantages.
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For many healthcare decisions, multiple alternatives are available with different combinations of advantages and disadvantages across several important dimensions.
A key issue is whether referendum formats with binary options are preferable to choice sets with multiple alternatives.
Building on these results and tools, we propose a novel approach for estimating potential outcomes for credit decisions with multiple alternatives based on matching on multiple propensity scores.
RFRS allows flexibility in both the number and identity of genes utilized from thousands to as few as 17 or eight genes, each with multiple alternatives.
The results show that (a) there is a natural interaction in the RDM task between similarity and the number of alternatives; (b) the number of alternatives influences "response caution", whereas the similarity between the alternatives influences "drift rate"; and (c) decisions in the RDM task are near optimal when participants are presented with multiple alternatives.
To this end, we developed a robust prognostic panel offering flexibility in both the number and identity of genes utilized from thousands to as few as eight genes, each with multiple alternatives to maximize the chance of successful migration to other assay technologies.
Many genes have multiple alternative transcripts with a different TSS.
Furthermore, if multiple alternative operons with different TSSs are transcribed in a sample, the assembled transcripts will be the possible longest alternative operon used in the sample.
In eukaryotic cells, GO annotations of related proteins to target genes revealed several processes through their domains that carry out diverse molecular functions and participate in multiple alternative interactions with other proteins, organelles, or locations in the cell (Table 4).
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