A data set used in QTL analysis will consist of a set of molecular marker scores and a set of phenotypic traits for each individual or line of the mapping population. Typically, a QTL data set will consist of 100 or more markers and five or more traits. A partial view of a data set for the Oregon Wolfe Barley population is shown in Table 1.
|
Marker Scores
|
Trait Values
|
Line
|
ABG704
|
Wx
|
MWG089
|
CDO475
|
plant height
|
days to heading
|
1
|
A
|
A
|
A
|
A
|
73.34
|
39.3
|
2
|
B
|
B
|
A
|
A
|
40.01
|
23.7
|
4
|
A
|
A
|
A
|
A
|
59.37
|
41.0
|
5
|
B
|
A
|
.
|
B
|
81.92
|
46.3
|
6
|
B
|
B
|
A
|
A
|
37.47
|
28.0
|
7
|
B
|
B
|
B
|
B
|
71.12
|
43.0
|
8
|
A
|
A
|
B
|
B
|
39.69
|
30.4
|
9
|
A
|
B
|
B
|
B
|
78.42
|
60.8
|
10
|
A
|
A
|
A
|
A
|
48.90
|
32.0
|
Table 1. A subset of marker scores and phenotypic traits for 10 lines of the Oregon Wolfe Barley population, http://barleyworld.org/oregonwolfe. A and B scores refer to the parental alleles at a marker locus, and a period indicates missing data. |
|
In addition to the marker and trait data, a marker linkage map is usually developed for each mapping population. A linkage map is required for simple and composite interval mapping, and is very useful, but not essential, for single-factor analysis of variance. Note the linkage map example (Fig. 7).