Figure 4

Detecting crossovers. A chromosomal SNP map for a recombinant progeny (clone A6AF) of a GT1 (type I) X CTG (type III) cross is represented, along with the published (triangles) and array-based (lines) genotyping calls for this clone. There is almost total agreement between markers called by both methods (>98.5%). The inset table summarizes the benefits of mapping crossovers using the array across 5 randomly selected progeny, showing that on average more breakpoints are discovered, and cover regions that are approximately 11-fold smaller. The numbers in parentheses in the breakpoint columns represent previous results using RFLP analysis.