Table 1B.

Description of In Silico Assignment of Microsatellite Markers to the Rat Genome


RNO

Markersa

e-PCR mappinga

Average spacing (kb)b

Inconsistencies (%)c
   1 1149 834 293.7 26 (3.1%)
   2 948 632 371.0 6 (0.9%)
   3 675 497 303.7 10 (2.0%)
   4 692 470 352.9 2 (0.4%)
   5 694 475 323.6 3 (0.6%)
   6 540 403 348.2 14 (3.5%)
   7 573 414 316.6 7 (1.7%)
   8 580 425 277.0 12 (2.8%)
   9 453 310 335.3 5 (1.6%)
10 686 480 215.4 5 (1.0%)
11 284 196 397.3 3 (1.5%)
12 307 205 215.0 4 (2.0%)
13 476 316 311.9 4 (1.3%)
14 355 258 377.8 3 (1.2%)
15 381 266 375.9 4 (1.5%)
16 315 223 372.8 2 (0.9%)
17 416 311 281.2 2 (0.6%)
18 325 234 342.5 2 (0.9%)
19 253 172 297.6 0 (0.0%)
20 194 123 389.4 1 (0.8%)
Unassigned 1289 853
Total
11,585
8097
270.4
115 (1.4%)

a The number of markers used for e-PCR mapping to the rat genome sequence includes all available microsatellites, including 1289 markers previously defined by a D-Number nomenclature (e.g., D0Got, D0Mco) that could not be assigned to a rat chromosome by genetic or RH mapping

b The average distance between markers in the genomic sequence was calculated with the chromosome length determined in the June 2003 rat genome assembly, and includes above-described markers that are only mapped by e-PCR

c Details of markers that are assigned to different chromosomes by linkage or RH mapping and e-PCR are available in our data repository (http://www.well.ox.ac.uk/rat_mapping_resources)