scholarly journals A first‐generation microsatellite linkage map of the ruff

2013 ◽  
Vol 3 (14) ◽  
pp. 4631-4640 ◽  
Author(s):  
Lindsay L. Farrell ◽  
Terry Burke ◽  
Jon Slate ◽  
David B. Lank
2004 ◽  
Vol 35 (3) ◽  
pp. 195-200 ◽  
Author(s):  
B. B. Kayang ◽  
A. Vignal ◽  
M. Inoue-Murayama ◽  
M. Miwa ◽  
J. L. Monvoisin ◽  
...  

Genetics ◽  
1996 ◽  
Vol 142 (2) ◽  
pp. 537-548 ◽  
Author(s):  
Michael W Nachman ◽  
Gary A Churchill

Abstract If loci are randomly distributed on a physical map, the density of markers on a genetic map will be inversely proportional to recombination rate. First proposed by MARY LYON, we have used this idea to estimate recombination rates from the Drosophila melanogaster linkage map. These results were compared with results of two other studies that estimated regional recombination rates in D. melanogaster using both physical and genetic maps. The three methods were largely concordant in identifying large-scale genomic patterns of recombination. The marker density method was then applied to the Mus musculus microsatellite linkage map. The distribution of microsatellites provided evidence for heterogeneity in recombination rates. Centromeric regions for several mouse chromosomes had significantly greater numbers of markers than expected, suggesting that recombination rates were lower in these regions. In contrast, most telomeric regions contained significantly fewer markers than expected. This indicates that recombination rates are elevated at the telomeres of many mouse chromosomes and is consistent with a comparison of the genetic and cytogenetic maps in these regions. The density of markers on a genetic map may provide a generally useful way to estimate regional recombination rates in species for which genetic, but not physical, maps are available.


Genetics ◽  
2004 ◽  
Vol 166 (1) ◽  
pp. 307-329 ◽  
Author(s):  
Paul B. Samollow ◽  
Candace M. Kammerer ◽  
Susan M. Mahaney ◽  
Jennifer L. Schneider ◽  
Scott J. Westenberger ◽  
...  

2011 ◽  
Vol 14 (2) ◽  
pp. 237-244 ◽  
Author(s):  
Sixin Liu ◽  
Caird E. Rexroad ◽  
Charlene R. Couch ◽  
Jan F. Cordes ◽  
Kimberly S. Reece ◽  
...  

2008 ◽  
Vol 39 (6) ◽  
pp. 623-634 ◽  
Author(s):  
D. A. Chistiakov ◽  
C. S. Tsigenopoulos ◽  
J. Lagnel ◽  
Y.-M. Guo ◽  
B. Hellemans ◽  
...  

BMC Genomics ◽  
2006 ◽  
Vol 7 (1) ◽  
Author(s):  
René Guyomard ◽  
Stéphane Mauger ◽  
Kamila Tabet-Canale ◽  
Sylvain Martineau ◽  
Carine Genet ◽  
...  

Heredity ◽  
2011 ◽  
Vol 107 (6) ◽  
pp. 530-536 ◽  
Author(s):  
J M Cano ◽  
M-H Li ◽  
A Laurila ◽  
J Vilkki ◽  
J Merilä

Genetics ◽  
2000 ◽  
Vol 155 (3) ◽  
pp. 1331-1345 ◽  
Author(s):  
Takashi Sakamoto ◽  
Roy G Danzmann ◽  
Karim Gharbi ◽  
Pamela Howard ◽  
Akiyuki Ozaki ◽  
...  

Abstract We constructed a genetic linkage map for a tetraploid derivative species, the rainbow trout (Oncorhynchus mykiss), using 191 microsatellite, 3 RAPD, 7 ESMP, and 7 allozyme markers in three backcross families. The linkage map consists of 29 linkage groups with potential arm displacements in the female map due to male-specific pseudolinkage arrangements. Synteny of duplicated microsatellite markers was used to identify and confirm some previously reported pseudolinkage arrangements based upon allozyme markers. Fifteen centromeric regions (20 chromosome arms) were identified with a half-tetrad analysis using gynogenetic diploids. Female map length is ~10 M, but this is a large underestimate as many genotyped segments remain unassigned at a LOD threshold of 3.0. Extreme differences in female:male map distances were observed (ratio F:M, 3.25:1). Females had much lower recombination rates (0.14:1) in telomeric regions than males, while recombination rates were much higher in females within regions proximal to the centromere (F:M, 10:1). Quadrivalent formations that appear almost exclusively in males are postulated to account for the observed differences.


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