Perhaps most importantly, the consensus map permitted the location of ten phenotypic traits controlled by major genes, QTL for seven quantitative traits and 51 gene-based markers, providing a valuable resource for the development of tools for MAS in rose.
The development of 2860 anchor markers and the construction of a high-resolution RH map permitted the successful localization of 480 of the assembled contigs to their chromosomal regions, representing 87%% (794.8 Mb) of the entire chromosome.
Hardware implementations of the VQ (vector quantization) and SOM (self organizing map) permit the deployment of these computationally intensive algorithms as single chips or IP cores.
Integration of the genetic and physical map permits the identification of several transcription units from within the narrowed LGMD1A interval, including one that is muscle specific, representing candidate genes for this familial dystrophy.
The strategic map permits the following perspectives to be interlinked: The financial perspective; The client/community perspective; The internal procedure perspective; The growth and staff learning perspective.
The adaptability of concept mapping permits the use of multiple modalities such as the addition of face-to-face brainstorming; use of qualitative methods, including structured interviews; and review and use of published literature and guidelines.
Genetic linkage maps permit the elucidation of genome structure and organization and enable the identification of molecular markers linked to traits in an experimental segregating progeny, leading ultimately to the elucidation of the genetic basis of the trait of interest.
High precision syntenic breakpoint mapping permits the evaluation, at least in principle, of whether or not these evolutionary breaks coincide with potential hotspots of chromosomal rearrangement such as fragile sites or cancer-associated breakpoints.
QTL mapping permits the identification of polymorphisms involved in trait variation in one or few pedigree populations, thereby reducing background genetic variations as well as the number and complexity of interacting alleles, while genetic association testing permits the identification of polymorphisms of more general value over a wider range of genetic backgrounds.
Linkage mapping permits the location of genes controlling traits of importance to chromosomes through their association with molecular markers and thus, represents a powerful tool for the positional cloning of major genes, the characterisation of quantitative trait loci (QTL), and the anchoring and ordering of contigs and scaffolds of both physical maps and genome sequence assemblies.
Since the KW test showed that the significant QTL on LG12 encompassed a large part of the LG at a significance level of p < 0.0001 (df = 1), an MQM analysis carried out on the condensed map permitted restriction of the locus to a corresponding 1.3 Mbp interval of the reference genome.
