Abstract
The a priori theoretical distribution of marker-linked quantitative effects in crosses involving inbred lines, and the number of quantitative loci contributing to such effects was obtained by numerical analysis, and examined as a function of the number and effects of the quantitative loci differentiating the lines, the location of the marker relative to the chromosome ends, and the mapping function. Over a wide range of assumptions it was found that the probability that a given marker will have an associated linked quantitative effect equal in magnitude to 0.2 phenotypic standard deviations or greater is of the order of 0-10 or more. In most of these cases it can be expected that the marker-linked effects will be due to one, or at the most two, quantitative loci in the vicinity of the marker.
Original language | English |
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Pages (from-to) | 179-190 |
Number of pages | 12 |
Journal | Heredity |
Volume | 43 |
Issue number | 2 |
DOIs | |
State | Published - Oct 1979 |
Externally published | Yes |