By Cristian Araneda, Roberto Neira, Natalia Lam (auth.), Thomas Kocher, Chittaranjan Kole (eds.)
Mapping of animal genomes has generated large databases and a number of other new recommendations and techniques, that are worthwhile to explain beginning, evolution and phylogeny. Genetic and actual maps of genomes additional offer special information on chromosomal place, functionality, expression and rules of academically and economically very important genes. The sequence Genome Mapping and Genomics in Animals offers finished and updated experiences on genomic study on a wide number of chosen animal platforms, contributed by way of prime scientists from round the world.
This quantity summarizes the 1st period of genomic reports of aquaculture species, within which the instruments and assets essential to help whole-genome sequencing have been built. those instruments will increase efforts towards selective breeding of aquaculture species. incorporated during this quantity are summaries of labor on salmonids, cyprinids, catfish, tilapias, eu sea bass, eastern flounder, shrimps and oysters.
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Extra info for Genome mapping and genomics in fishes and aquatic animals
Differences in recombination rates between sexes are well documented and have been explained by lower frequencies of crossing over in the heterogametic sex. Apparently, in salmonid ﬁshes, this is increased by the formation of multivalents only in males. Evidence from rainbow and brown trout shows that in males, large chromosomal regions proximal to the centromere have recombination frequencies close to zero, in comparison with telomeric regions that exhibit higher recombination rates (Sakamoto et al.
A second QTL was mapped to linkage group OA-XXVII, where six AFLP markers (between GGTCCC60 and GATCC510) and three SSR loci (OmyFGT-1TUF, Ssa94NVH, and OtsG3) showed signiﬁcant association. A third QTL region was anchored in linkage group OA-III close to eight AFLP markers (from GCTCTC178 to GATCAG291) and three SSR loci (One8ASC, OMM1054, and Ogo2Ui/W; Table 6). These three regions bearing presumptive QTLs on the malebased map have been conﬁrmed in a separate analysis of three other families (Rodriguez et al.
1 Bulked Segregant Analysis In BSA, the co-segregation of many markers is followed in a segregating population obtained by crossing a single pair of parental ﬁsh with different phenotypic expressions for the discrete trait under study. A number of segregating individuals are used in each pool, with the objective of minimizing variation not associated with the trait of interest (Michelmore et al. 1991). This approach was used to identify sex-speciﬁc sequence characterized ampliﬁed region (SCAR) markers Omy-163 and OmyP9 linked to the Y chromosome in rainbow trout using AFLP screening (Felip et al.