Map Error Reduction Using Genetic and Sequence-Based Physical Maps to Order Closely Linked Markers

• Published in: Human heredity Vol. 54; no. 1; pp. 34 - 44
• Main Authors: DeWan, Andrew T., Parrado, Antonio R., Matise, Tara C., Leal, Suzanne M.
• Format: Journal Article
• Language: English
• Published: Basel, Switzerland S. Karger AG 01.01.2002
• Subjects: Genetic Linkage; Genetic Markers; Humans; Original Paper; Physical Chromosome Mapping; Fine mapping; Map errors; Comprehensive genetic maps; Sequence-based physical maps
• ISSN: 0001-5652; 1423-0062
• DOI: 10.1159/000066697

The Marshfield comprehensive genetic maps are frequently used for linkage and association studies, however, for some regions of these maps the marker order has low level of likelihood ratio support. In order to investigate the level of statistical support and the accuracy of the genetic maps compared to sequence-based physical maps, two ~30 cM autosomal regions were selected. The first region was selected from chromosome 3 and consisted predominately of draft sequence. The second region was selected from chromosome 21 and consisted of finished sequence data. The physical order of these markers was based upon their position on Celera (CEL) and Human Genome Project-Santa Cruz (HGP-sc) sequence-based physical maps. The chromosome 3 and 21 regions contained 100 and 61 markers, respectively, on the Marshfield genetic map. The genetic and physical map order was consistent for 88.9 and 89.2% of the markers in the region on chromosome 3 and 21, respectively. Using a novel scoring criterion to assess inconsistent marker order between genetic and physical maps, it was determined that the physical order was likely the correct order for 3.3 and 7.1% of the markers in the chromosome 3 and 21 regions, respectively. To increase the accuracy of the order of markers selected for fine mapping a method is presented which combines information from genetic and sequence-based physical maps.