A simple method for combining genetic mapping data from multiple crosses and experimental designs.

PLoS One · 2007 · PMC2001185 · PMID 17940600

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barely significantno p-value reported

In addition, combining loci that are barely significant or narrowly miss the criteria for significance in multiple populations can clearly lead to strong observations of new loci or improved confidence in previously known loci.

also in 875 other papers

highly significantno p-value reported

This is particularly useful when a simple cross with highly significant loci is being considered since the software used to sort P-values (OutParser.py) runs in approximately N 2 time with respect to number of permutations.

also in 132,142 other papers

Quoted from the open-access full text in Europe PMC under the licence the publisher applied. The sentence is reproduced exactly as published; the emphasis is ours.