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Intriguingly, three WNT-related maps (listed in 2, 15 and 16 of Table 1) were enriched.
There were 33 markers with conflicting chromosome locations among the CSS-F2, CSS-RIL and CSH-RIL maps (listed in Additional file 2: Table S5).
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In total, 15,514 polymorphic markers were used for quantitative trait locus (QTL) mapping (listed in Table S2).
Plasmid maps were listed in Additional file 1: Figure S1.
Cellular processes with the corresponding number of maps are listed in Table 3.
The numerical values of all connectivity maps are listed in Supplementary Table 1.
The EC numbers used for generating maps are listed in Additional file 10, showing the normalized counts for Unitrans and R values for the different cross-comparisons between treatments.
QTLs detected from consensus and parental maps are listed in Tables 3 and 4, Additional file 8: Table S6 and Additional file 9: Table S7 (main features of stable QTLs only), and Additional file 10: Table S8 and Additional file 11: Table S9 (detailed features of all QTLs).
The locus name and genetic map position for all SNP loci in the 29 LGs of genetic map are listed in Supplementary Table S4.
Based on the mapping relations listed in Table 1, the failure rate of a component can be generated randomly between the areas.
The 70 PathExpand interactors not present in the original CCKR map are listed in Table 3.
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